Metamemory (FOK) in Episodic Memory Post TBI - Schmitter-Edgecombe & Anderson Washington

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Neuropsychology Copyright 2007 by the American Psychological Association

2007, Vol. 21, No. 2, 224 –234 0894-4105/07/$12.00 DOI: 10.1037/0894-4105.21.2.224

Feeling of Knowing in Episodic Memory Following Moderate to Severe


Closed-Head Injury
Maureen Schmitter-Edgecombe Jonathan W. Anderson
Washington State University Eastern Washington University

The ability to accurately monitor one’s memory is a metacognitive process that is important in everyday
life. The authors examined episodic memory feeling-of-knowing (FOK) ratings in 21 moderate to severe
closed-head injury (CHI) participants (more than 1 year postinjury) and 21 controls. Participants
studied 36 critical cue–target word pairs. Following a brief delay, they were asked to recall the target that
corresponded to a given cue. Confidence ratings were made for recalled words, and FOK judgments were
This article is intended solely for the personal use of the individual user and is not to be disseminated broadly.

made for nonrecalled words in terms of the likelihood of recognizing the target word on a subsequent
This document is copyrighted by the American Psychological Association or one of its allied publishers.

recognition test. CHI participants demonstrated less accurate recall but accurate ability to judge their
recall performance (retrospective memory monitoring). They also demonstrated intact FOK judgments
when providing binary judgments but demonstrated difficulties making finer discriminations on an
ordinal scale (prospective memory monitoring). These findings suggest that memory monitoring is not a
unitary construct. It is proposed that CHI participants may display intact memory monitoring when
predictions are based on familiarity assessment but not when continued probing for additional episodic
information is required.

Keywords: traumatic brain injury, memory monitoring, metamemory, metacognition

People’s ability to accurately monitor information stored in Early studies investigating metamemory accuracy following CHI
memory is a metacognitive ability that has considerable impor- generally suggest that CHI individuals tend to overestimate their
tance in everyday life. For example, faced with failure when memory abilities (Boake, Freeland, Ringholz, Nance, & Edwards,
attempting to recall information from memory, individuals must 1995; Port, Willmott, & Charlton, 2002; Roche, Fleming, & Shum,
decide the extent to which the information seems readily accessi- 2002; Sbordone, Seyranian, & Ruff, 1998). However, several vari-
ble and, consequently, whether they should continue an effort to ables appear to moderate this outcome. A less severe head injury
retrieve it (Koriat, 2000). Within the closed-head injury (CHI) (Leathem, Murphy, & Flett, 1998; Sherer et al., 1998), a greater time
literature, although deficits in episodic memory have been well since injury (Allen & Ruff, 1990; Sunderland, Harris, & Baddeley,
documented (e.g., Knight, Harnett, & Titov, 2005; Levin, Gold- 1983), and a nondepressed mood state (Boake et al., 1995), for
stein, High, & Eisenberg, 1988; Vanderploeg, Crowell, & Curtiss, example, all have been found to lead to better memory self-awareness
2001), few studies have evaluated the cognitive mechanisms by
following CHI. In these early studies, metamemory accuracy was
which metamemory judgments are made. This is an important area
most commonly investigated by contrasting CHI patients’ self-ratings
of study as it has been suggested that inaccurate metamemory can
of their memory functioning with objective test findings or with
impede a person’s ability to benefit from rehabilitation (Herbert &
Powell, 1989; Lam, McMahon, Priddy, & Gehred-Schulz, 1988). ratings made by family members and rehabilitation staff (Flemming,
In addition, several case studies have shown that providing feed- Strong, & Ashton, 1996). More recently, metamemory abilities fol-
back and review about memory performance can improve the lowing CHI have been investigated using experimental techniques
metamemory accuracy of individuals with CHI (Giacino & Cice- that require participants to make estimates about their memory per-
rone, 1998; Schlund, 1999). In this study, we used a feeling-of- formance in close temporal proximity to the memory task (e.g.,
knowing (FOK) paradigm and confidence level ratings to investi- Kennedy, 2004; Kennedy & Nawrocki, 2003; Kennedy & Yorkston,
gate the prospective and retrospective memory monitoring abilities 2000; Schmitter-Edgecombe & Woo, 2004). Such measurement tech-
of moderate to severe CHI participants at the time of retrieval. niques include eliciting global predictions, in which judgments are
made about how many items from a study list will subsequently be
recalled, and item-by-item predictions, in which predictions are made
about the likelihood of subsequent recall for individual items.
Maureen Schmitter-Edgecombe, Department of Psychology, Washing- In a recent study that elicited global memory predictions, Schmit-
ton State University; Jonathan W. Anderson, Department of Psychology, ter-Edgecombe and Woo (2004) found that metamemory was better
Eastern Washington University. preserved than actual memory performance in participants who suf-
This study was partially supported by Grant R01 NS47690 from the fered a severe CHI. In that study, participants with severe CHI (more
National Institute of Neurological Disease and Stroke. We thank Matthew
than 1 year postinjury) and controls predicted their recall for verbal
Wright and Ellen Woo for their support in coordinating data collection. We
also thank the members of the Head Injury Research Team for their help in
and visual material both prior to and following experience with the
collecting and scoring the data. memory tasks. Although CHI participants exhibited poorer recall than
Correspondence concerning this article should be addressed to Maureen controls, this study found that both groups were equally self-aware of
Schmitter-Edgecombe, Department of Psychology, Washington State Uni- how differing task demands influenced their recall. That is, both CHI
versity, Pullman, WA 99164-4820. E-mail: schmitter-e@wsu.edu and control participants predicted better recall for material presented

224
FEELING-OF-KNOWING JUDGMENTS AFTER CHI 225

multiple times as opposed to on a single occasion and for material that 1992; Marquié & Huet, 2000). The FOK ratings, on the other hand,
would be recalled immediately as opposed to after a delay. Both represent a prospective judgment about whether the participant will
groups also successfully modified their predictions following task later recognize a studied target item that could not be brought to
exposure, indicating that the CHI participants were able to self- consciousness at that moment. By obtaining confidence level ratings
monitor their performances and use experience to derive more accu- in addition to FOK judgments, we were able to examine both retro-
rate memory performance expectations. spective and prospective memory monitoring accuracy. Previous re-
The results of a series of studies conducted by Kennedy and search has demonstrated dissociations between retrospective and pro-
colleagues (Kennedy, 2001; Kennedy & Nawrocki, 2003; Kennedy & spective monitoring accuracy, with intact recall confidence and im-
Yorkston, 2000) also suggest that moderate to severe CHI individuals paired prospective memory monitoring being found in both
maintain the ability to accurately monitor episodic information during Alzheimer’s disease patients and patients with lesions in the frontal
learning. These studies used the judgment-of-learning (JOL) proce- lobe (Pappas et al., 1992; Schnyer et al., 2004). Consistent with
dure, which requires participants, at the end of a learning trial or after previous literature (e.g., Schmitter-Edgecombe, Marks, Wright, &
a short delay, to make item-by-item judgments regarding the likeli- Ventura, 2004; Vanderploeg et al., 2001), we expected that partici-
pants with CHI would perform more poorly than controls on the
This article is intended solely for the personal use of the individual user and is not to be disseminated broadly.

hood that they will remember specific learned information on a


This document is copyrighted by the American Psychological Association or one of its allied publishers.

subsequent memory test. Kennedy and Nawrocki (2003) found that episodic recall and recognition tasks. Prior research suggests that
when making delayed JOL predictions about subsequent recall for moderate to severe CHI participants can successfully monitor their
acquired narrative information (i.e., 2 min after narrative presenta- performances at the time of learning (Kennedy & Yorkston, 2000;
tion), both the CHI and control groups were more accurate in pre- Schmitter-Edgecombe & Woo, 2004) and that they can demonstrate
dicting recall for stated information than for implied information. intact recall confidence accuracy for newly learned episodic informa-
Furthermore, Kennedy and Yorkston (2000) showed that CHI and tion (Kennedy, 2001). The purpose of this study was to investigate
control participants were very accurate in making delayed JOL pre- whether moderate to severe CHI participants would also exhibit intact
dictions (i.e., 2– 4 min after presentation) about their ability to later prospective memory as well as retrospective memory monitoring
recall word pairs but were inaccurate when making predictions im- abilities at the time of retrieval.
mediately after studying the word pairs. These findings suggest that, As a secondary aim of this study, we investigated the relation
similar to controls, participants with CHI are able to benefit from the among episodic memory FOK, retrospective memory monitoring, and
opportunity to self-monitor items successfully stored in memory at the executive–frontal and medial–temporal functions. Prior research sug-
time of learning. gests that frontal cortical structures are involved in predictions about
The present study expands previous item-by-item memory mon- episodic memory retrieval in the FOK paradigm (Janowsky, Shi-
itoring research in the CHI population by investigating memory mamura, & Squire, 1989; Schnyer, Nicholls, & Verfaellie, 2005;
monitoring at the time of retrieval using an FOK paradigm. In the Schnyer et al., 2004; Souchay et al., 2000). For example, the results of
typical FOK procedure (Hart, 1965), participants are asked to FOK judgment research with brain-injured patients (Janowsky et al.,
estimate the likelihood that they will subsequently recognize a 1989) and a recent functional magnetic resonance imaging study
piece of information that they had failed to recall either from (Schnyer et al., 2005) suggest that the prefrontal cortex plays an
semantic memory or from recently learned episodic memory (e.g., important role in monitoring the contents of memory. Souchay et al.
T. O. Nelson & Narens, 1990; Souchay, Isingrini, & Espagnet, (2000) also showed that age-related decline in episodic memory FOK
2000). To evaluate FOK accuracy as an expression of participants’ accuracy could partially be accounted for by a composite score of
actual metamemorial knowledge, FOK ratings are compared with various tests of executive abilities. In addition to executive–frontal
success or failure on a recognition test. Unlike JOLs, which are functions, research conducted with individuals with focal temporal
made during the study phase and are thought to rely heavily on lobe epilepsy suggests that medial temporal lobe dysfunction can
participants’ prior knowledge of variables that will influence their impact FOK accuracy (Prevey, Delaney, & Mattson, 1988; Prevey,
memory performance, FOKs are made after the recall attempt and Delaney, Mattson, & Tice, 1991). Consistent with this notion,
are thought to reflect participants’ capacity to monitor their per- Souchay, Isingrini, and Gil (2002) recently found that episodic mem-
formance by generating and using feedback from their memory ory deficits were a more important factor than executive functions in
performance (Bieman-Copland & Charness, 1994). Consequently, explaining the FOK inaccuracy found in Alzheimer’s disease patients.
FOK judgments have been viewed as involving a computation In cases of moderate to severe CHI, both the prefrontal cortex and the
process in which the by-product of the retrieval process is used to temporal lobe area have a higher probability of being damaged as
evaluate the ease of future access to the answer (Koriat & Levy- compared with other areas of the cortex (Adams et al., 1989; Schnei-
Sadot, 2001; Souchay & Isingrini, 2004; Souchay et al., 2000). bel & Levin, 1997; Wilson, Hadley, Wiedmann, & Teasdale, 1995).
In the present study, moderate to severe CHI and control partici- By examining the pattern of associations among FOK accuracy,
pants learned cue–target word pairs. Following a distractor task, they retrospective memory monitoring, and neuropsychological tests sen-
were presented with the cue words and asked to recall the target sitive to executive–frontal functions and medial–temporal functions,
words. For those items they were unable to recall, participants were we may uncover information about those factors that contribute to
asked to provide an FOK judgment about the likelihood that they metamemorial judgments following moderate to severe CHI.
would be able to recognize the correct answer among a number of
alternatives. For those items to which they produced an answer, Method
participants provided a confidence level rating about their recall
Participants
attempt (Costermans, Lories, & Ansay, 1992). The confidence level
ratings represent a retrospective judgment about whether a provided Twenty-one individuals (6 female, 15 males) who had suffered
answer has been correctly recalled from memory (Costermans et al., a moderate to severe CHI and 21 neurologically normal controls (9
226 SCHMITTER-EDGECOMBE AND ANDERSON

female, 12 male) were the participants in this study. The majority scores on the Shipley Institute of Living Scale (Zachary, 1991)
of participants with CHI were identified through patient records revealed slightly poorer performance by the CHI group
obtained from a regional traumatic brain injury rehabilitation pro- (M ⫽ 98.90, SD ⫽ 8.61) compared with the control group (M ⫽
gram in Spokane, Washington. Others were recruited through 105.10, SD ⫽ 6.66), t(40) ⫽ 2.59, p ⬍ .05.
presentations made at several head injury support groups. This To characterize the CHI population and highlight those areas in
experiment was completed as part of a larger test battery that which the CHI group was experiencing residual cognitive difficul-
included standardized neuropsychological tests and other experi- ties, we administered a battery of neuropsychological tests. As can
mental measures (see Schmitter-Edgecombe & Bales, 2005; be seen in Table 1, consistent with the typical cognitive sequelae
Schmitter-Edgecombe & Kayne, 2006). The participants with CHI of a moderate to severe CHI, the CHI participants performed more
received feedback regarding their cognitive functioning in return poorly than the controls on tests assessing attention and speeded
for their time. processing (Symbol Digit Modalities Test, Smith, 1991; Trail
Participants were considered to have suffered a moderate to Making Test—Part A, Reitan, 1958), immediate and delayed ver-
severe CHI if review of medical records indicated that (a) depth of bal memory (California Verbal Learning Test [CVLT], Delis,
Kramer, Kaplan, & Ober, 1987; Wechsler Memory Scale—III
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coma, as assessed by the Glasgow Coma Scale (Teasdale &


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Jennett, 1974), was 12 or less (n ⫽ 13) or (b) duration of coma was [WMS–III], Wechsler, 1997b), and executive functioning (Trail
greater than 2 hr (n ⫽ 5). In the three cases for which we were Making Test—Part B [Trails B], Reitan, 1958; Letter–Number
unable to obtain medical records, both the participant and a sig- Sequencing subtest from the WAIS–III, Wechsler, 1997a; Con-
nificant other reported a coma duration of 5 days or greater. In trolled Oral Word Association Test, Benton & Hamsher, 1976). In
addition, duration of posttraumatic amnesia (PTA), assessed ret- contrast to the above performances, the groups did not differ
rospectively by careful clinical questioning of the participant, significantly on a confrontation naming test (Test of Adolescent/
was 7 days or longer for all CHI participants (M ⫽ 90 days, SD ⫽ Adult Word Finding, German, 1990) or in perseverative respond-
111; range ⫽ 7–390); 76% of participants reported PTAs of more ing on an executive functioning task (Wisconsin Card Sorting Test
than 2 weeks, and 67% of more than 4 weeks. [WCST], Heaton, 1981).
All participants with CHI were assessed at least 1 year following
injury (M ⫽ 6.92 years, SD ⫽ 6.72; range ⫽ 1–22) and were Stimuli
experiencing residual cognitive deficits; 71% were more than 2
Two sets of cue–target word pair stimuli were constructed. Each
years postinjury, and 33% were more than 6 years postinjury. The
stimulus set contained the same 36 cue words but a different target
majority of participants with CHI had suffered their head injuries
word. The target words were low associates to the cue words. The
as a result of a motor vehicle or motorcycle accident (n ⫽ 17), with
target words were balanced across stimulus sets in terms of cue-
the remaining injuries resulting from either a fall of greater than 10
to-target strength (Set A: .011–.019; Set B: .011–.019), word
feet (n ⫽ 3) or a bicycle accident (n ⫽ 1). To minimize possible
frequency (Set A: 1–72 per million; Set B: 1– 82 per million), and
developmental effects on performance, we included in the CHI
concreteness (Set A: 5.05– 6.76; Set B: 5.13– 6.96; D. L. Nelson,
group only individuals who were at least 16 years old at the time
McEvoy, & Schreiber, 1998). The target words from both stimulus
of injury (range ⫽ 17–50 years) and less than 55 years old at
sets were used in the recognition test along with four other dis-
testing (range ⫽ 18 –52 years). Participants were excluded from
tracter words that were also low associates to each cue word
the study if they had a preexisting neurological, psychiatric, or
(cue-to-target strength ⫽ .011–.22). During study, each cue word
developmental disorder (or disorders) other than a CHI, a history
was presented in black lowercase letters in 36-point Times font
of treatment for substance abuse, or a history of multiple head
on 8.5 ⫻ 5.5-in. paper. Each target word was presented directly
injuries. All participants demonstrated adequate visual acuity as
below the cue word in black uppercase 36-point Times font. A
indicated by a Snellen ratio of at least .50 at a distance of 41 cm.
total of eight additional cue–target word pairs were created; four
Six of the control participants were neurologically normal un-
pairs were added to the beginning and end of each stimulus set to
dergraduate students participating as a requirement for course
minimize primacy and recency effects. These cue–target buffer
credit. The remaining 15 control participants were recruited from
pairs remained constant across each stimulus set. Assignment to
the community through the use of advertisement. In return for their
stimulus set was counterbalanced within each group.
participation, they received monetary compensation. To increase
the likelihood that the CHI participants’ premorbid abilities were
Procedure
roughly equivalent to those of the controls, we closely matched the
age (M ⫽ 33.14, SD ⫽ 10.51) and educational level (M ⫽ 13.14, Each participant completed a study phase and a test phase. For
SD ⫽ 1.62) of the CHI participants to the age (M ⫽ 29.58, the study phase, participants were told that they would be pre-
SD ⫽ 10.75) and educational level (M ⫽ 13.76, SD ⫽ 1.81) of the sented with cue–target word pairs and that their task was to learn
control participants (ts ⬍ 1.2). In addition, an estimate of premor- the target words. They were told to use the cue word (printed in
bid Wechsler Adult Intelligence Scale—Revised (WAIS–R) Full lowercase letters) to help them learn the corresponding target word
Scale Intelligence Quotient (FSIQ) derived from the Barona index (printed in uppercase letters) because the memory test would
equation (Barona, Reynolds, & Chastain, 1984), which takes into involve presenting them with the cue word and asking for the
account six demographic variables (i.e., age, sex, race, education, corresponding target word. Each cue–target word pair was pre-
occupation, and region), revealed that the CHI (M ⫽ 106.50, sented for 6 s. The cue–target word pairs were presented in the
SD ⫽ 4.77) and control (M ⫽ 105.36, SD ⫽ 7.53) groups did not same order for all participants.
differ significantly in premorbid abilities, t(40) ⫽ 0.56. At the time Following the study phase, participants completed the Symbol
of study, the WAIS–R FSIQ estimate derived from participants’ Digit Modalities Test, which took approximately 8 min to admin-
FEELING-OF-KNOWING JUDGMENTS AFTER CHI 227

Table 1
Demographic Data and Mean Summary Data for the Closed-Head Injury and Control Groups
M SD N

Test variable CHI Con CHI Con CHI Con Cohen’s d

Demographics
Age 33.14 29.58 10.51 10.75 21 21 ⫺0.34
Education 13.14 13.76 1.62 1.81 21 21 0.37
Gender 6 F, 15 M 9 F, 12 M
Estimated premorbid FSIQa 105.36 106.50 4.77 7.53 21 21 0.18
Intellectual ability/word finding
WAIS–R estimated FSIQb 98.90 105.10* 8.61 6.66 20 21 0.83
TAWF total correct 33.55 34.48 3.20 1.72 20 21 0.37
Attention/speeded processing
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SDMT total oral correct 54.53 69.00** 17.27 14.80 20 20 0.94


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SDMT total written correct 47.30 59.95** 13.48 11.83 21 20 1.01


Trails A (time) 34.62 22.24* 23.01 6.46 21 21 ⫺0.75
Verbal memory
CVLT Trials 1–5 40.14 55.71*** 15.87 9.20 21 21 1.23
CVLT Long-Delay Free Recall 7.65 12.33*** 4.49 2.33 20 21 1.35
WMS–III Logical Memory I 35.90 45.38** 10.46 9.43 21 21 0.97
WMS–III Logical Memory II 19.43 28.81*** 9.22 6.70 21 21 1.19
Executive functioning
Trails B (time) 82.50 49.33** 51.49 17.62 20 21 ⫺0.89
WAIS–III L-N Sequencing 9.48 12.10** 3.46 2.34 21 21 0.91
COWAT total correct 32.95 41.20* 10.00 10.61 20 20 0.82
WCST-64 Perseverative Errors 7.67 6.33 6.35 2.48 18 21 ⫺0.29

Note. Unless otherwise indicated, mean scores are raw scores. CHI ⫽ closed-head injury; Con ⫽ control;
FSIQ ⫽ Full Scale Intelligence Quotient; WAIS–R ⫽ Wechsler Adult Intelligence Scale—Revised; TAWF ⫽
Test of Adult Word Finding; SDMT ⫽ Symbol Digit Modalities Test; Trails A ⫽ Trail Making Test—Part A;
CVLT ⫽ California Verbal Learning Test; WMS–III ⫽ Wechsler Memory Scale—Third Edition; Trails B ⫽
Trail Making Test—Part B; WAIS–III ⫽ Wechsler Adult Intelligence Scale—Third Edition; L-N ⫽ Letter–
Number; COWAT ⫽ Controlled Oral Word Association Test (Form PRW); WCST ⫽ Wisconsin Card Sorting
Test.
a
Estimated premorbid Wechsler Adult Intelligence Scale—Revised FSIQ was based on the Barona index
equation (Barona, Reynolds, & Chastain, 1984), which takes into account the following six demographic
variables: age, sex, race, education, occupation, and region.
b
Estimated Wechsler Adult Intelligence Scale—Revised FSIQ was derived from participants’ total score on the
Shipley Institute of Living Scale (Zachary, 1991).
*
p ⬍ .05. ** p ⬍ .01. *** p ⬍ .001.

ister. For the test phase, participants were first presented one-by- Results
one with the cue word in the same type font as during study and
given 15 s to produce the corresponding target word. Whenever a Episodic Memory Performance: Recall and Recognition
potential target word was produced, participants were asked to Before recall and recognition performances of the CHI and
make a level-of-confidence rating about the correctness of their
control groups were compared, raw data were converted to mean
answer using a 7-point rating scale (1 ⫽ I am not at all sure that
proportional data. As expected, the data revealed poorer recall and
my answer is correct to 7 ⫽ I am absolutely sure that my answer
recognition performance by the CHI participants. The mean pro-
is correct). Whenever participants were unable to think of the
portion of answers provided during the cued recall task was
target word, they were asked to make an FOK judgment about their
ability to correctly recognize the target word from among six significantly greater for the control group (M ⫽ .66, SD ⫽ .20)
words when presented with the cue word. FOK ratings were also compared with the CHI group (M ⫽ .46, SD ⫽ .21), t(40) ⫽ 3.13,
made on a 7-point Likert scale, ranging from 1 (I am absolutely p ⬍ .005. Of the answers provided, the mean proportion of
sure that I will not recognize the correct answer) to 7 (I am successfully recalled target words was also significantly greater for
absolutely sure that I will recognize the correct answer). The the controls (M ⫽ .80, SD ⫽ .20) compared with the CHI partic-
testing phase did not begin until the experimenter was sure that the ipants (M ⫽ .62, SD ⫽ .32), t(40) ⫽ 2.13, p ⬍ .05. The proportion
participants understood what they were supposed to do. The sec- of correct answers on the recognition task similarly differed be-
ond part of the test phase involved having participants complete tween the groups, with the CHI group (M ⫽ .68, SD ⫽ .24)
the recognition test for all 36 items, not just the subset of items for recognizing proportionally fewer of the target words than the
which they had made FOK judgments. Participants were given a control group (M ⫽ .85, SD ⫽ .14), t(40) ⫽ 2.84, p ⬍ .01.
sheet of paper with the cue words in the left-hand column, and they Furthermore, the CHI group (M ⫽ .59, SD ⫽ .26) recognized
were asked to circle the corresponding target word for each cue proportionally fewer items that they provided FOK judgments for
word. The cue words for the recall and recognition tests were than the control group (M ⫽ .73, SD ⫽ .20), t(40) ⫽ 1.96, p ⬍ .05.
presented in the same order. In contrast, for those target items that were unsuccessfully re-
228 SCHMITTER-EDGECOMBE AND ANDERSON

called, both groups showed proportionally similar levels of recog- used. That is, because confidence judgments were rated on a
nition (for CHI participants, M ⫽ .67, SD ⫽ .33; for controls, M ⫽ 7-point scale, gamma was calculated by casting the frequency of
.65, SD ⫽ .32). responses into a 2 (recall: correct or incorrect) ⫻ 7 (ratings: 1, 2, 3,
4, 5, 6, and 7) contingency table. The cell frequencies, or number
of cases per each cell of the 2 ⫻ 7 table, were then entered as a
Retrospective Memory Monitoring
weight variable, and gamma was calculated through the Crosstabs
Confidence ratings. Before comparing the confidence level option of SPSS 12.01 (SPSS, 1999). Owing to limitations of the
(CL) judgments of the CHI and control groups, we evaluated gamma statistic (Schraw, 1995), participants who had used only
whether the two groups had used the CL rating scale in a similar one or two of the ratings were eliminated from the analysis.
fashion. The percentages of ratings falling into the different cate- Therefore, 5 controls and 3 CHI participants could not be included
gories were entered into a 2 (group: CHI or control) ⫻ 7 (rating: 1, in the group comparison of the gamma statistic. An independent-
2, 3, 4, 5, 6, and 7) mixed-model analysis of variance (ANOVA). samples t test conducted on the gamma coefficient revealed that
The analysis revealed a main effect for ratings, F(6, 240) ⫽ 39.73, the CHI group (M ⫽ .64, SD ⫽ .56) and the control group (M ⫽
MSE ⫽ 259.61, p ⬍ .001. Tests of simple effects indicated a .75, SD ⫽ .35) did not differ significantly in level of association
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between CL ratings and recall performance (t ⬍ 1; see Table 2). In


This document is copyrighted by the American Psychological Association or one of its allied publishers.

greater use of the I am absolutely sure that my answer is correct


category (M ⫽ 48%) as compared with all other categories ( ps ⬍ addition, the gamma correlations for both groups indicated a strong
.001). In addition, the category ratings for My answer is most likely association between recall performance and CL judgments, with
correct (M ⫽ 16%), My answer might be correct (M ⫽ 13%), and the gamma index being significantly above zero for both the CHI
My answer is just as likely to be correct as incorrect (M ⫽ 10%) group, t(17) ⫽ 4.87, p ⬍ .001, and the control group, t(15) ⫽ 8.64,
were used more often than the category ratings for My answer p ⬍ .001.
might be incorrect (M ⫽ 6%), My answer is most likely incorrect Unlike the gamma coefficient, which assesses the joint proba-
(M ⫽ 3%), and I am not at all sure that my answer is correct (M ⫽ bility of judgments and memory performance, the Hamann coef-
4%) ( ps ⬍ .05). There was no significant main effect of group ficient requires each of the ratings and memory performances to be
(F ⬍ 1) or Group ⫻ Rating interaction (F ⬍ 1), indicating that the treated as mutually exclusive probabilities and provides a measure
CHI and control groups had used the CL rating scale in a quali- of agreement accuracy between ratings and memory performance
tatively similar way. (Schraw, 1995). Because of the need for binary data to compute
Because the CHI and control groups had distributed their ratings this statistic, CL ratings were clustered, with ratings 1– 4 consid-
across the CL scale in a similar way, we then determined whether ered not confident and ratings 5–7 considered confident. Because
participants had assigned higher CL ratings to words that they had of the additive function of this statistic, all 21 participants could be
correctly recalled as compared with incorrectly recalled words. A used in the analysis. Evaluation of the Hamann coefficient revealed
total of 5 control participants and 2 CHI participants who never that the CHI group (M ⫽ .53, SD ⫽ .39) did not differ significantly
produced an incorrect target word could not be included in this from the control group (M ⫽ .69, SD ⫽ .27) in the accuracy of
analysis. The group (CHI or control) by recall (correct or incorrect) retrospective judgment. The Hamann index was also greater than
mixed-model ANOVA revealed that the mean CL rating assigned chance for both the CHI, t(20) ⫽ 6.30, p ⬍ .001, and control,
to target words that were correctly recalled (M ⫽ 6.17, SD ⫽ 0.12) t(20) ⫽ 11.62, p ⬍ .001, groups. These findings indicate that,
was significantly higher than the mean CL rating assigned to similar to controls, the CHI participants were able to reliably
incorrectly recalled target words (M ⫽ 4.56, SD ⫽ 0.25), F(1, identify those target words that they had successfully recalled from
33) ⫽ 41.84, MSE ⫽ 1.08, p ⬍ .001. There was no significant those that they had unsuccessfully recalled.
main effect of group (F ⬍ 1). In addition, there was no significant
interaction between group and recall (F ⬍ 1), as the discrepancy
Prospective Memory Monitoring
between mean ratings for correctly and incorrectly recalled target
words was similar for the CHI (difference ⫽ 1.82) and control FOK ratings. Similar to the procedure used with the CL rat-
(difference ⫽ 1.40) groups. These findings indicate that both ings, the percentages of FOK ratings falling into the different
groups were able to show discrimination between successfully categories were entered into a 2 (group: CHI or control) ⫻ 7
recalled and unsuccessfully recalled target words. (ratings: 1, 2, 3, 4, 5, 6, and 7) mixed-model ANOVA to determine
Measures of association and agreement accuracy. Consistent whether the CHI and control groups had used the FOK scale in a
with recent metacognitive literature (e.g., Souchay, Isingrini, similar manner. Results indicated a main effect for ratings, F(6,
Clarys, Taconnat, & Eustache, 2002, 2004), to determine both 240) ⫽ 7.85, MSE ⫽ 470.25, p ⬍ .001. Follow-up tests of simple
degree of association (i.e., the degree to which levels of one effects indicated a greater use of the I might recognize the correct
variable covary with levels of a second variable) and relative answer category (M ⫽ 33%) than all other categories ( ps ⬍ .01).
accuracy (i.e., the degree to which judgments match correct and In addition, the category ratings for I will most likely recognize the
incorrect performance) between CL ratings and recall perfor- correct answer (M ⫽ 20%), I am just as likely to recognize as to
mance, we calculated the Goodman–Kruskal gamma correlation not recognize the correct answer (M ⫽ 15%), and I might not
and the Hamann coefficient, respectively (see T. O. Nelson, 1984; recognize the correct answer (M ⫽ 12%) were used more than
Schraw, 1995). Both the gamma and Hamann coefficients are category ratings I am absolutely sure that I will recognize the
nonparametric correlation measures that range from –1 to 1, with 0 correct answer (M ⫽ 8%), I will most likely not recognize the
corresponding to no association (gamma) or chance levels of correct answer (M ⫽ 8%), and I am absolutely sure that I will not
accuracy (Hamann). recognize the correct answer (M ⫽ 4%) ( ps ⬍ .05). Of note, there
For the gamma calculation, the original CL rating values were was no significant main effect of group (F ⬍ 1) or indication of a
FEELING-OF-KNOWING JUDGMENTS AFTER CHI 229

Table 2
Means for Confidence Levels and Feeling-of-Knowing Ratings and Gamma and Hamann Indices
for the Closed-Head Injury and Control Groups
M SD N

Test variable CHI Con CHI Con CHI Con Cohen’s d

Confidence level ratings


Correct recalla 6.03 6.32 0.87 0.46 19 16 0.41
Incorrect recalla 4.63 4.50 1.67 1.35 19 16 0.08
Gamma indexb .64 .75 .56 .35 18 16 0.25
95% CI .39–.89 .59–.91
Hamann index .53 .69 .39 .27 21 21 0.49
95% CI .40–.76 .59–.89
Feeling-of-knowing ratings
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Correct recognitionc 4.48 4.86 1.41 0.98 18 17 0.31


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Incorrect recognitionc 4.10 4.33 1.17 0.94 18 17 0.21


Gamma indexb .19 .48* .44 .38 17 17 0.73
95% CI ⫺.01–.39 .31–.65
Hamann index .20 .26 .41 .46 21 21 0.14
95% CI .01–.39 .05–.47

Note. CHI ⫽ closed-head injury; Con ⫽ control; CI ⫽ confidence interval.


a
Participants who never produced an incorrect target word were removed from analysis.
b
Owing to limitations of the gamma statistic (Schraw, 1995), gamma coefficients could not be computed for
participants who had used only one or two of the ratings.
c
Participants who either successfully recognized, or did not recognize (CHI ⫽ 1), all target words for which they
had made a feeling-of-knowing judgment were removed from analysis.
*
p ⬍ .05.

Group ⫻ Rating interaction (F ⬍ 1). This suggests that both An independent-samples t test of the gamma coefficient for
groups used the FOK rating scale in a qualitatively similar way. prospective memory monitoring revealed that control participants’
A mixed-model ANOVA was then used to determine whether overall gamma coefficient (M ⫽ .48, SD ⫽ .38) showed a signif-
participants assigned higher FOK ratings to words they later suc- icantly higher level of association between FOK judgments and
cessfully recognized. A total of 4 control participants and 3 CHI recognition performance than that of the CHI participants (M ⫽
participants could not be included in this analysis because they .19, SD ⫽ .44), t(32) ⫽ 2.07, p ⬍ .05. In addition, whereas the
either successfully recognized, or did not recognize (CHI ⫽ 1), all level of association between FOK judgments and recognition was
target words for which they had made an FOK judgment. The significantly above chance for the control participants,
group (CHI or control) by recognition (correct or incorrect) anal- t(16) ⫽ 5.20, p ⬍ .001, the level of association did not differ
ysis revealed a significant main effect of recognition, F(1, significantly from “zero” or “no association” for the CHI partici-
33) ⫽ 15.37, MSE ⫽ 0.14, p ⬍ .001, that was modified by a pants (t ⫽ 1.80). To compute the Hamann coefficient, ratings were
significant Group ⫻ Recognition interaction, F(1, 33) ⫽ 5.89, again clustered, with FOK ratings 1– 4 coded as not likely to be
MSE ⫽ 0.14, p ⬍ .05. Evaluation of the interaction revealed that recognized and FOK ratings 5–7 coded as likely to be recognized.
the control participants made higher FOK ratings for target words In contrast to the gamma index, the Hamann coefficient did not
that they later correctly recognized (M ⫽ 4.86, SD ⫽ 0.98) indicate a significant difference between the CHI (M ⫽ .20, SD ⫽
compared with those they incorrectly recognized (M ⫽ 4.33, .41) and control (M ⫽ .26, SD ⫽ .46) groups in the accuracy of
SD ⫽ 0.94), t(16) ⫽ 3.78, p ⬍ .005. In contrast, CHI participants FOK judgments (t ⬍ 1). In addition, the Hamann coefficients were
did not show a significant difference in their FOK ratings for significantly above chance for both the CHI group, t(20) ⫽ 2.21,
correctly recognized (M ⫽ 4.48, SD ⫽ 1.41) and incorrectly p ⬍ .05, and the control group, t(20) ⫽ 2.54, p ⬍ .05. These
recognized (M ⫽ 4.10, SD ⫽ 0.94) target words, t(17) ⫽ 1.33, p ⬎ findings suggest that the CHI participants showed adequate accu-
.20. There was no significant main effect of group (F ⫽ 1.22). This racy in FOK judgments concerning whether they would success-
index of prospective memory monitoring indicates that the CHI fully recognize a target but demonstrated difficulties discriminat-
group experienced more difficulty than the control group in cor- ing their ratings along an ordinal scale. Furthermore, correlational
rectly predicting those target words that they would later success- analyses revealed that FOK gamma and FOK Hamann were not
fully recognize. significantly related for the CHI participants (r ⫽ .23). For the
Measures of association and agreement accuracy. Similar to control group, FOK Hamann and FOK gamma were significantly
the procedure followed for retrospective memory monitoring, we correlated (r ⫽ .69, p ⬍ .005).
calculated the gamma and Hamann statistics to determine the
degree of association and relative accuracy between FOK ratings
Correlations With Neuropsychological Variables
and recognition performance. Again, owing to the limitations of
the gamma coefficient, a gamma index could not be computed Correlations were calculated to examine the relationship be-
for 4 controls and 4 CHI participants. All 21 participants were used tween retrospective and prospective memory monitoring ability
in the calculation of the Hamann index. and the memory and executive measures shown in Table 3. The
230 SCHMITTER-EDGECOMBE AND ANDERSON

Table 3
Correlations Among the Neuropsychological Tests Sensitive to Memory and Executive Functioning and the Gamma and Hamann
Coefficients for the Closed-Head Injury (CHI) Group and the CHI and Control Groups Combined
CHI CHI and controls

CL FOK CL FOK

Test variable Gamma Hamann Gamma Hamann Gamma Hamann Gamma Hamann

Verbal memory
CVLT Trials 1–5 .13 .24 .32 .31 .25 .34* .39* .16
CVLT Long-Delay Free Recall ⫺.04 .38 .27 .38 .03 .41* .39* .12
WMS–III Logical Memory I .14 .38 .28 .25 .10 .31* .35* .22
WMS–III Logical Memory II ⫺.07 .39 .30 .48* .08 .39* .34* .33*
Composite score .04 .35 .33 .37 .13 .40** .40* .23
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Executive functioning
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Trails B (time) ⫺.24 ⫺.56* ⫺.20 ⫺.18 ⫺.31 ⫺.48** ⫺.25 ⫺.18
WAIS–III L-N Sequencing .04 .36 .09 .01 .09 .38 .33 .11
COWAT Total Correct ⫺.23 .07 .27 .08 .04 .21 .17 .09
WCST–64 Perseverative Errors ⫺.06 ⫺.28 ⫺.02 ⫺.55* ⫺.17 ⫺.24 ⫺.15 ⫺.36
Composite score .08 .45* .16 .33 .20 .45** .30 .26

Note. Values are partial correlations controlling for age. CL ⫽ confidence-level judgments; FOK ⫽ feeling-of-knowing judgments; CVLT ⫽ California
Verbal Learning Test; WMS–III ⫽ Wechsler Memory Scale—Third Edition; Trails B ⫽ Trail Making Test—Part B; WAIS–III ⫽ Wechsler Adult
Intelligence Scale—Third Edition; L-N ⫽ Letter–Number; COWAT ⫽ Controlled Oral Word Association Test (Form PRW); WCST ⫽ Wisconsin Card
Sorting Test.
*
p ⬍ .05. ** p ⬍ .01.

analyses were first conducted for the CHI participants and then, to the executive functioning composite (rs ⫽ .01 to .33) or the
maximize the statistical power of our analyses, for both the CHI memory composite (rs ⫽ –.01 to .37). For both groups combined,
and the control participants. Because the measures represented raw significant correlations were observed between the CL Hamann
scores, we attempted to reduce the confounding effects of age by index and both the memory (r ⫽ .40, p ⬍ .01) and executive
partialing out age in all of the correlational analyses conducted. functioning (r ⫽ .45, p ⬍ .01) composites. A significant correla-
For the CHI participants, a significant correlation was observed tion was also observed between the FOK gamma index and the
between the CL index and Trails B (r ⫽ –.56, p ⬍ .05). Significant memory composite (r ⫽ .40, p ⬍ .05). No other correlations
correlations were also observed between the FOK Hamann index reached significance for either the executive functioning composite
and WMS–III Logical Memory II (r ⫽ .48, p ⬍ .05) and WCST (rs ⫽ .09 to .30) or the memory composite (rs ⫽ .02 to .29).
Perseverative Errors (r ⫽ –.55, p ⬍ .05). No other correlations Because the memory score appeared to be a reliable predictor of
were significant (rs ⫽ –.24 to .32). For the CHI and control
FOK gamma performance, which was the one measure in which
participants combined, the CL Hamann index correlated signifi-
the CHI participants performed more poorly than the controls, we
cantly with all four of the memory measures (rs ⫽ .34 to .41, ps ⬍
attempted to evaluate the role of memory as a mediator of
.05) and with Trails B (r ⫽ –.48, p ⬍ .01) and Letter–Number
metamemory monitoring differences between the CHI and control
Sequencing (r ⫽ .38, p ⬍ .05). The FOK gamma index also
correlated significantly with all four of the memory measures (rs ⫽ participants. To do this, we used an analysis of covariance. If
.34 to .39, ps ⬍ .05). In addition, significant correlations were memory capacity mediates the CHI effect on FOK gamma, remov-
observed between the FOK Hamann index and Logical Memory II ing the composite memory score should reduce the CHI effect on
(r ⫽ .33, p ⬍ .05) and WCST Perseverative Errors (r ⫽ –.36, p ⬍ FOK gamma. The analysis revealed that when the memory com-
.05). No other correlations were significant (rs ⫽ –.31 to .32). posite score was controlled for, the difference between the CHI
We then examined the roles of memory and executive function- and control groups was no longer significant, F(1, 31) ⫽ 0.65, p ⬎
ing as mediators of memory monitoring ability. The neuropsycho- .40. The adjusted means of FOK gamma for the CHI and control
logical tests sensitive to frontal– executive functioning (Trails B groups were .27 and .41, respectively.
time; WAIS–III Letter–Number Sequencing; Controlled Oral
Word Association Test, total number of words; and WCST Perse-
Correlations With Injury Characteristics
verative Errors) and memory functioning (CVLT Total Recalled,
Trials 1–5; CVLT Long-Delay Free Recall; WMS–III Logical Correlations were also conducted for the CHI participants be-
Memory I and II) were converted to z scores and then averaged. tween the prospective (FOK gamma and Hamann) and retrospec-
The four measures of memory (rs ⫽ .69 to .92) and of executive tive (CL gamma and Hamann) measures of memory monitoring
functioning (rs ⫽ .45 to .69) were well correlated. All composite and injury characteristics (i.e., time since injury and severity of
measures were scaled so that better performance was reflected by injury). No significant correlations emerged between the memory
higher values. For the CHI participants, the composite measure of monitoring measures and either time since injury (rs ⫽ –.31 to .30)
executive functioning correlated with the CL Hamann index (r ⫽ or injury severity as assessed by self-reported length of PTA (rs ⫽
.45, p ⬍ .05). No other correlations reached significance for either –.22 to –.10). In addition, no significant correlations were found
FEELING-OF-KNOWING JUDGMENTS AFTER CHI 231

between the neuropsychological tests sensitive to memory and from an ordinal scale, the gamma statistic is more sensitive than
either time since injury (rs ⫽ .03 to .29) or PTA (rs ⫽ –.17 to .38). the Hamann index to the distribution of scores. These findings
indicate that although chronic (more than 1 year postinjury), mod-
erate to severe CHI participants showed adequate accuracy in FOK
Discussion
judgments concerning whether they would successfully recognize
This study expands previous research by investigating, at the a target, they demonstrated difficulties discriminating their ratings
time of memory retrieval, both retrospective and prospective mem- along an ordinal scale.
ory monitoring abilities in a CHI population. The CHI participants Consistent with other studies that have shown dissociations
in this study all had suffered moderate to severe brain injuries, between retrospective and prospective memory monitoring abili-
were greater than 1 year postinjury, and were exhibiting residual ties in clinical populations (e.g., Pannu, Kaszniak, & Rapcsak,
neuropsychological impairments at the time of testing. The CHI 2005; Pappas et al., 1992; Schnyer et al., 2004), these data indicate
and control participants learned cue–target word pairs and, after a that memory monitoring is not a unitary function. These data
distractor task, were asked to recall each target word when pre- further suggest that FOK decisions are based, in part, on some
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sented with the corresponding cue word. Whenever participants abilities that are not tapped by simple recall confidence. Koriat and
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produced an answer to a cue word, they were asked to provide a Levy-Sadot (2001) proposed that accurate FOK retrieval predic-
confidence rating about their memory performance. This confi- tions involve a cascading two-step process beginning with assess-
dence rating, which reflected participants’ judgment about whether ment of the relative familiarity of the cue (Metcalfe, 1993; Reder
the retrieved word was the correct target word, served as our & Ritter, 1992) and ending with an effortful accessibility assess-
measure of retrospective memory monitoring. If participants did ment (Koriat, 1993, 1997). In the first step, if cue familiarity is
not provide an answer, they made an FOK judgment about whether low, then a fast “don’t know” response may be initiated (Klin,
they believed they would be able to recognize the target word from Guzman, & Levine, 1997); the target is discounted (i.e., feeling of
among a group of distractor items. FOKs reflect judgments about not knowing) and memory search is discontinued. In contrast, if
whether sought after information is still in memory even though it the cue elicits partial familiarity about the target, memory interro-
cannot be retrieved at the moment, and the FOK judgment served gation is initiated (Reder, 1987). This second step is hypothesized
as our measure of prospective memory monitoring. to involve a deliberate search process during which a relative sense
In line with past research, the CHI group’s recall and recogni- of the accessibility of the memory is evaluated on the basis of the
tion for the studied material was poorer than that of the control amount of ease and access to partial clues (e.g., fragments of the
group. Despite demonstrating impairment in episodic memory, the target, semantic and episodic attributes), regardless of whether the
CHI participants did not differ significantly from controls in their clues are correct. According to Koriat and Levy-Sadot (2001), cue
ability to assign confidence ratings to their recall performance. familiarity and accessibility may contribute to FOK judgments
That is, the CHI and control groups demonstrated similar levels of either independently or interchangeably.
judgment accuracy and association between recall performance In terms of abilities involved in recall confidence ratings, Coster-
and CL judgments, and both groups assigned higher CL ratings to mans et al. (1992) hypothesized that because CL judgments are
correct as compared with incorrect recall attempts. In addition, for required only when a tentative target word is produced, partici-
both groups, the measures assessing memory monitoring accuracy pants may use the strength of the link between the cue and target
(i.e., CL Hamann) and association (i.e., CL gamma) were well to generate a CL estimate. However, this option does not exist for
above chance, and participants were highly confident in the ratings FOK ratings. Schnyer et al. (2004) recently suggested that the
given to correctly recalled targets (i.e., My answer is most likely initial stage of FOK judgments may tap processes similar to those
correct). These findings demonstrate that despite impairments in involved in confidence ratings. That is, these authors hypothesized
episodic memory, participants with moderate to severe CHIs were that the ability to evaluate cue familiarity may be functionally
able to show accurate retrospective memory monitoring abilities similar to the ease-of-generation assessment proposed as the basis
for retrieved items. of confidence ratings. On the basis of their finding of intact
In regard to prospective memory monitoring ability, we found confidence judgments and impaired FOK ratings in patients with
that when assessing the relative accuracy of predictions (i.e., frontal lobe lesions, Schnyer et al. proposed that these patients may
Hamann index), CHI participants’ FOK judgments about their display an intact ability to monitor recall accuracy and retrieval
future memory performance did not differ from controls. That is, predictions on the basis of familiarity assessment but fail when
the degree to which FOK judgments, when dichotomized into monitoring requires continued probing for additional episodic in-
likely to be recognized (ratings 5–7) and not likely to be recognized formation. If this model is correct, then similar to frontal lobe
(ratings 1– 4), matched subsequent correct and incorrect recogni- patients, our data suggest, CHI participants may experience greater
tion performance was above chance and similar for the CHI and monitoring difficulty than controls when memory monitoring in-
control participants. In contrast, analysis of the degree of covaria- volves evaluating the ease of future accessibility to an answer.
tion between FOK judgments and recognition performance re- Similar to the retrospective confidence levels used in the present
vealed a lower level of association for the CHI participants com- study, Kennedy and Yorkston (2000) found that CHI and control
pared with controls. Furthermore, unlike for controls, the CHI participants did not differ in their memory accuracy predictions
participants’ gamma coefficient was no better than chance, indi- when predicting memory performance following retrieval at-
cating no association between FOK judgments and recognition tempts. Using the JOL procedure, Kennedy and colleagues
performance. In addition, unlike the controls, the CHI participants (Kennedy, 2001; Kennedy & Nawrocki, 2003; Kennedy & York-
did not assign higher FOK ratings to target words that were later ston, 2000) have also consistently shown that moderate to severe
correctly as compared with incorrectly recognized. Computed CHI individuals maintain the ability to accurately monitor episodic
232 SCHMITTER-EDGECOMBE AND ANDERSON

information during learning. The current data extend this previous measure may be partially mediated by episodic memory perfor-
research by showing that participants with CHI may experience mance in moderate to severe CHI participants.
prospective memory monitoring difficulties when making judg- The study data also appear to suggest that the requirements
ments at the time of retrieval. Unlike FOK judgments, which are involved in making subtle distinctions along an ordinal scale are
believed to begin with the assessment of the cue and then, if there more influenced by episodic memory abilities than those involved
is a sufficient degree of familiarity, shift to an accessibility assess- in making binary yes–no distinctions. This may be so because the
ment of memory (Koriat & Levy-Sadot, 2001), JOL predictions ability to make finer discriminations regarding the likelihood that
are thought to be best accommodated by cue-familiarity theory a solicited target is retained in memory and will be recognized at
(Koriat, 1997). Therefore, the overall pattern of findings in the CHI a later time requires greater reliance on the ability to conduct an
metamemorial judgment literature is consistent with the idea that effortful, deliberate search of clues available in memory. As Koriat
CHI participants may experience difficulties when monitoring (1993, 1997) suggested, FOK predictions can be conceptualized as
being based on a partial product of retrieval memory operations.
requires continued probing for additional episodic information but
Given that participants had only 15 s to produce a corresponding
not when recall accuracy and retrieval predictions are based on
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target word, it could be that the CHI participants’ prospective


familiarity assessment.
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monitoring performance was limited by the amount of partial clues


Our data are also consistent with Schraw’s (1995) suggestion
that could be brought to mind during that limited time frame and/or
that the gamma and Hamann indices do not measure exactly the by the use of less efficient strategic retrieval strategies. Both of
same phenomenon and that both should be examined in FOK these possibilities would limit the amount of information that may
research. More specifically, we found that the CHI and control be needed to accurately capture the degree of covariation between
groups’ prospective memory monitoring performance differed sig- recognition performance and FOK judgments. The role that mem-
nificantly when measured with the gamma index but not when ory difficulties may play in metamemory performance is currently
assessed with the Hamann coefficient. In addition, no significant in need of further exploration. In an early study, Janowsky et al.
correlation between the gamma and Hamann indices was found for (1989) found that patients with Korsakoff’s syndrome were unable
the CHI participants. According to Schraw, the Hamann index is a to make accurate FOK judgments about newly learned sentences
more appropriate measure of judgment accuracy whereas the following a 5-min delay, whereas participants with frontal lobe
gamma index is more appropriate for capturing the degree of lesions were impaired only after a 1–3-day delay when the mem-
covariation between recognition performance and FOK judgments. ory trace was weakened. These authors hypothesized that frontal
Thus, it appears that although the CHI participants in this study lobe lesions and memory impairment together may result in more
were able to determine at a gross level whether they would be able severe metamemory difficulties than frontal lobe lesions alone.
to correctly recognize the answer at a future time point (perhaps by Consistent with this hypothesis, in a recent comprehensive review
relying on cue familiarity), they had difficulty making finer dis- of metamemory experiments in neurological populations, Pannu
criminations about the accuracy of subsequent memory retrieval and Kaszniak (2005) found that the patient groups that had mem-
along an ordinal rating scale. ory loss in addition to frontal dysfunction (e.g., Alzheimer’s de-
Recently, Souchay et al. (2004) suggested that the Hamann mentia, Korsakoff’s syndrome) performed the most poorly on
index can be taken as a more sensitive measure of FOK judgments metamemory tasks.
than the gamma statistic. They based this conclusion on their The participants with CHI in this study all had experienced
finding that the Hamann coefficient was more highly correlated diffuse brain damage as a result of a moderate to severe CHI in
with executive functioning in older adults than the gamma index. young to middle adulthood. In addition, they all were Caucasian
Although we found no significant association between our frontal– individuals who were more than 1 year postinjury and had recov-
executive composite and either the FOK gamma index or the ered to a cognitive level that allowed for semi-independent to
Hamann index, we did find for the CHI group that perseverative independent living. Furthermore, none of the participants were in
errors on the WCST correlated significantly with the Hamann the demented range of functioning. Participants were also recruited
measure. This may suggest that perseverative responding is more retrospectively from a rehabilitation center and from support
highly related to poor metamemory abilities than other compo- groups. Therefore, generalizability may not extend well to indi-
nents of frontal lobe functioning. However, we also found that the viduals with CHI who experience focal frontal lobe lesions or to
correlation coefficient involving the frontal– executive composite those whose cognitive deficits are so severe that they are unable to
was substantially higher for FOK Hamann (r ⫽ .33) than for FOK integrate and maintain knowledge regarding their own functioning.
gamma (r ⫽ .16). This may suggest that executive functioning In addition, in the present study we investigated FOK accuracy on
deficits play a more prominent role in explaining FOK inaccuracy an episodic memory task that involved recognition predictions
than in capturing the degree of covariation between recognition about newly learned information. Given that episodic FOK accu-
performance and FOK judgments. Consistent with this notion, for racy and semantic FOK accuracy (i.e., predictions about informa-
the CHI and control participants combined, we found that our tion already stored in memory) have been found to dissociate in
memory composite measure and all four of our measures of some clinical populations (e.g., Brandt, 1985; Janowsky et al.,
episodic memory ability correlated significantly with the FOK 1989; Souchay et al., 2002) and have been hypothesized to depend
gamma index but not with the FOK Hamann index. Furthermore, differentially on frontal functions (Souchay et al., 2002; Souchay,
after we covaried out the memory composite measure (Schnyer et Bacon, & Danion, 2006), future studies are needed to investigate
al., 2004), the CHI group’s gamma index was above chance and semantic FOK and/or directly contrast semantic and episodic FOK
did not differ from that of the control group. These findings accuracy following moderate to severe CHI. Furthermore, because
suggest that for episodic memory FOK tasks, the FOK gamma this research was conducted in a laboratory setting and involved
FEELING-OF-KNOWING JUDGMENTS AFTER CHI 233

item-by-item predictions for cue–target word pairs, the generaliz- German, D. J. (1990). National College of Education Test of Adolescent/
ability of these findings to real-world situations that involve ret- Adult Word Finding. Austin, TX: PRO-ED.
rospective and prospective memory monitoring remains to be Giacino, J. T., & Cicerone, K. D. (1998). Varieties of deficit unawareness
explored. Given the impact that inaccurate metamemory can have after brain injury. Journal of Head Trauma Rehabilitation, 13, 1–15.
Hart, J. T. (1965). Memory and the feeling-of-knowing experience. Journal
on a person’s ability to benefit from rehabilitation, future studies
of Educational Psychology, 56, 208 –216.
are needed to better understand issues related to metamemory
Heaton, R. K. (1981). A manual for the Wisconsin Card Sorting Test.
following brain injury, especially in the early phases of recovery. Odessa, FL: Psychological Assessment Resources.
In conclusion, we used an FOK procedure and CL ratings to Herbert, C. M., & Powell, G. E. (1989). Insight and progress in rehabili-
investigate prospective and retrospective memory monitoring abil- tation. Clinical Rehabilitation, 3, 125–130.
ities in a moderate to severe CHI population that was more than 1 Janowsky, J. S., Shimamura, A. P., & Squire, L. R. (1989). Memory and
year postinjury. We found that despite impaired episodic memory metamemory: Comparisons between patients with frontal lobe lesions
performance, the CHI participants demonstrated accurate retro- and amnesic patients. Psychobiology, 17, 3–11.
spective memory monitoring abilities for recalled items. Prospec- Kennedy, M. R. T. (2001). Retrospective confidence judgments made by
This article is intended solely for the personal use of the individual user and is not to be disseminated broadly.

tive memory monitoring abilities were found to be intact when adults with traumatic brain injury: Relative and absolute accuracy. Brain
This document is copyrighted by the American Psychological Association or one of its allied publishers.

assessed by binary judgments about whether an item that could not Injury, 15, 469 – 487.
be retrieved would be recognized but not when finer discrimina- Kennedy, M. R. T. (2004). Self-monitoring recall during two tasks after
tions were required on an ordinal scale. These findings indicate traumatic brain injury: A preliminary study. American Journal of
that the difficulties the moderate to severe CHI participants expe- Speech-Language Pathology, 13, 142–154.
rienced with prospective memory monitoring are not part of a Kennedy, M. R. T., & Nawrocki, M. D. (2003). Delayed predictive accuracy
more global monitoring deficit and that FOK predictions are in- of narrative recall after traumatic brain injury: Salience and explicitness.
fluenced by abilities that are not tapped by simple recall confi- Journal of Speech, Language, and Hearing Research, 46, 98 –112.
dence. To account for the pattern of study findings, we hypothe- Kennedy, M. R. T., & Yorkston, K. M. (2000). Accuracy of metamemory
after traumatic brain injury: Predictions during verbal learning. Journal
sized that CHI participants were functionally similar to controls
of Speech, Language, and Hearing Research, 43, 1072–1086.
when making accurate monitoring judgments based either on the
Klin, C. M., Guzman, A. E., & Levine, W. H. (1997). Knowing that you
strength of the link between cue and retrieved target or on cue
don’t know: Metamemory and discourse processing. Journal of Exper-
familiarity, but that they appeared to deteriorate when prospective
imental Psychology: Learning, Memory, and Cognition, 23, 1378 –1393.
monitoring judgments required continued probing for additional Knight, R. G., Harnett, M., & Titov, N. (2005). The effects of traumatic
episodic information. Future research will be needed to further brain injury on the predicted and actual performance of a test of pro-
evaluate the plausibility of this hypothesis and the role that mem- spective remembering. Brain Injury, 19, 27–38.
ory loss plays in metamemory performance. Koriat, A. (1993). How do we know that we know? The accessibility model
of the feeling of knowing. Psychological Review, 100, 609 – 639.
Koriat, A. (1997). Monitoring one’s own knowledge during study: A
References cue-utilization approach to judgments of learning. Journal of Experi-
Adams, J. H., Doyle, D., Ford, I., Gennarelli, T. A., Graham, D. I., & mental Psychology: General, 126, 349 –370.
McLellan, D. R. (1989). Diffuse axonal injury in head injury: Definition, Koriat, A. (2000). Control processes in remembering. In E. Tulving & C.
diagnosis, and grading. Histopathology, 15, 49 –59. Fergus (Eds.), The Oxford handbook of memory (pp. 333–346). New
Allen, C. C., & Ruff, R. M. (1990). Self-rating versus neuropsychological York: Oxford University Press.
performance of moderate versus severe head-injured patients. Brain Koriat, A., & Levy-Sadot, R. (2001). The combined contributions of the
Injury, 4, 7–17. cue-familiarity and accessibility heuristics to feelings of knowing. Journal
Barona, A., Reynolds, C. R., & Chastain, R. (1984). A demographically of Experimental Psychology: Learning, Memory, and Cognition, 27, 34 –53.
based index of premorbid intelligence for the WAIS–R. Journal of Lam, C. S., McMahon, B. T., Priddy, D. A., & Gehred-Schulz, A. (1988).
Consulting and Clinical Psychology, 52, 885– 887. Deficit awareness and treatment performance among traumatic head
Benton, A., & Hamsher, K. (1976). Multilingual aphasia examination. injury adults. Brain Injury, 2, 235–242.
Iowa City: University of Iowa Press. Leathem, J. M., Murphy, L. J., & Flett, R. A. (1998). Self- and informant-
Bieman-Copland, S., & Charness, N. (1994). Memory knowledge and ratings on the Patient Competency Rating Scale in patients with trau-
memory monitoring in adulthood. Psychology and Aging, 9, 287–302. matic brain injury. Journal of Clinical and Experimental Neuropsychol-
Boake, C., Freeland, J. C., Ringholz, G. M., Nance, M. L., & Edwards, ogy, 20, 694 –705.
K. E. (1995). Awareness of memory loss after severe closed-head injury. Levin, H. S., Goldstein, F. C., High, W. M., & Eisenberg, H. M. (1988).
Brain Injury, 9, 273–283. Disproportionately severe memory deficit in relation to normal intellec-
Brandt, J. (1985). Access to knowledge in the dementia of Huntington’s tual functioning after closed head injury. Journal of Neurology, Neuro-
disease. Developmental Neuropsychology, 1, 335–348. surgery, & Psychiatry, 51, 1294 –1301.
Costermans, J., Lories, G., & Ansay, C. (1992). Confidence level and Marquié, J. C., & Huet, N. (2000). Age differences in feeling-of-knowing
feeling of knowing in question answering: The weight of inferential and confidence judgments as a function of knowledge domain. Psychol-
processes. Journal of Experimental Psychology: Learning, Memory, and ogy and Aging, 15, 451– 461.
Cognition, 18, 142–150. Metcalfe, J. (1993). Novelty monitoring, metacognition, and control in a
Delis, D. C., Kramer, J. H., Kaplan, E., & Ober, B. A. (1987). California composite holographic associative recall model: Implications for Kor-
Verbal Learning Test: Adult version [Manual]. San Antonio, TX: Psy- sakoff amnesia. Psychological Review, 100, 3–22.
chological Corporation. Nelson, D. L., McEvoy, C. L., & Schreiber, T. A. (1998). The University
Flemming, J. M., Strong, J., & Ashton, R. (1996). Self-awareness of of South Florida word association, rhyme, and word fragment norms.
deficits in adults with traumatic brain injury: How best to measure? Retrieved January 15, 2003, from http://w3.usf.edu/FreeAssociation/
Brain Injury, 10, 1–16. Intro.html
234 SCHMITTER-EDGECOMBE AND ANDERSON

Nelson, T. O. (1984). A comparison of current measures of the accuracy of Goldman-Rakic (Eds.), Development of the prefrontal cortex: Evolution,
feeling-of-knowing predictions. Psychological Bulletin, 95, 109 –133. neurobiology, and behavior (pp. 241–260). Baltimore: Brookes Publish-
Nelson, T. O., & Narens, L. (1990). Metamemory: A theoretical framework ing.
and new findings. In G. H. Bower (Ed.), The psychology of learning and Schnyer, D. M., Nicholls, L., & Verfaellie, M. (2005). The role of VMPC
motivation (pp. 125–173). New York: Academic Press. in metamemorial judgments of content retrievability. Journal of Cogni-
Pannu, J. K., & Kaszniak, A. W. (2005). Metamemory experiments in tive Neuroscience, 17, 832– 846.
neurological populations: A review. Neuropsychology Review, 15, 105– Schnyer, D. M., Verfaellie, M., Alexander, M. P., LaFleche, G., Nicholls,
130. L., & Kaszniak, A. W. (2004). A role for right medial prefrontal cortex
in accurate feeling-of-knowing judgments: Evidence from patients with
Pannu, J. K., Kaszniak, A. W., & Rapcsak, S. Z. (2005). Metamemory for
lesions to frontal cortex. Neuropsychologia, 42, 957–966.
faces following frontal lobe damage. Journal of the International Neu-
Schraw, G. (1995). Measures of feeling-of-knowing accuracy: A new look
ropsychological Society, 11, 668 – 676.
at an old problem. Applied Cognitive Psychology, 9, 321–332.
Pappas, B. A., Sunderland, T., Weingartner, H. M., Vitiello, B., Martinson,
Sherer, M., Boake, C., Levin, E., Silver, B. V., Ringholz, G., & High,
H., & Putnam, K. (1992). Alzheimer’s disease and feeling-of-knowing W. M., Jr. (1998). Characteristics of impaired awareness after traumatic
for knowledge and episodic memory. Journals of Gerontology, 47, brain injury. Journal of the International Neuropsychological Society, 4,
This article is intended solely for the personal use of the individual user and is not to be disseminated broadly.

159 –164. 380 –387.


This document is copyrighted by the American Psychological Association or one of its allied publishers.

Port, A., Willmott, C., & Charlton, J. (2002). Self-awareness following Smith, A. (1991). Symbol Digit Modalities Test. Los Angeles: Western
traumatic brain injury and implications for rehabilitation. Brain In- Psychological Services.
jury, 16, 277–289. Souchay, C., Bacon, E., & Danion, J. M. (2006). Metamemory in schizo-
Prevey, M. L., Delaney, R. C., & Mattson, R. H. (1988). Metamemory in phrenia: An exploration of feeling-of-knowing state. Journal of Clinical
temporal lobe epilepsy: Self-monitoring of memory functioning. Brain and Experimental Neuropsychology, 28, 828 – 840.
and Cognition, 7, 298 –311. Souchay, C., & Isingrini, M. (2004). Age-related differences in the relation
Prevey, M. L., Delaney, R. C., Mattson, R. H., & Tice, D. M. (1991). between monitoring and control of learning. Experimental Aging Re-
Feeling-of-knowing in temporal lobe epilepsy: Monitoring knowledge search, 30, 179 –193.
inaccessible to conscious recall. Cortex, 27, 81–92. Souchay, C., Isingrini, M., Clarys, D., Taconnat, L., & Eustache, F. (2004).
Reder, L. M. (1987). Strategy selection in question answering. Cognitive Executive functioning and judgment-of-learning versus feeling-of-
Psychology, 19, 90 –138. knowing in older adults. Experimental Aging Research, 30, 47– 62.
Reder, L. M., & Ritter, F. E. (1992). What determines initial feeling of Souchay, C., Isingrini, M., & Espagnet, L. (2000). Aging, episodic memory
knowing? Familiarity with question terms, not with the answer. Journal feeling-of-knowing, and frontal functioning. Neuropsychology, 14, 299 –
309.
of Experimental Psychology: Learning, Memory, and Cognition, 18,
Souchay, C., Isingrini, M., & Gil, R. (2002). Alzheimer’s disease and
435– 451.
feeling-of-knowing in episodic memory. Neuropsychologia, 40, 2386 –
Reitan, R. M. (1958). Validity of the Trail Making Test as an indicator of
2396.
organic brain damage. Perceptual and Motor Skills, 8, 271–276.
SPSS. (1999). SPSS Base 9.0 user’s guide. Chicago: Author.
Roche, N. L., Fleming, J. M., & Shum, D. H. K. (2002). Self-awareness of Sunderland, A., Harris, J. E., & Baddeley, A. D. (1983). Do laboratory tests
prospective memory failure in adults with traumatic brain injury. Brain predict everyday memory? A neuropsychological study. Journal of
Injury, 16, 931–945. Verbal Learning and Verbal Behavior, 22, 341–357.
Sbordone, R. J., Seyranian, G. D., & Ruff, R. M. (1998). Are subjective Teasdale, G., & Jennett, B. (1974). Assessment of coma and impaired
complaints of traumatically brain injured patients reliable? Brain In- consciousness. A practical scale. Lancet, 13, 81– 84.
jury, 12, 505–515. Vanderploeg, R. D., Crowell, T. A., & Curtiss, G. (2001). Verbal learning
Schlund, M. W. (1999). Self awareness: Effects of feedback and review on and memory deficits in traumatic brain injury: Encoding, consolidation,
verbal self reports and remembering following brain injury. Brain In- and retrieval. Journal of Clinical and Experimental Neuropsychol-
jury, 13, 375–380. ogy, 23, 185–195.
Schmitter-Edgecombe, M., & Bales, J. W. (2005). Understanding text after Wechsler, D. (1997a). Wechsler Adult Intelligence Scale—Third edition.
severe closed-head injury: Assessing inferences and memory operations San Antonio, TX: Harcourt Assessment.
with a think-aloud procedure. Brain and Language, 94, 331–346. Wechsler, D. (1997b). Wechsler Memory Scale—Third edition. San Anto-
Schmitter-Edgecombe, M., & Kayne, M. (2006). Costs of a predictable nio, TX: Harcourt Assessment.
switch between simple cognitive tasks following severe closed-head Wilson, J. T. L., Hadley, D. M., Wiedmann, K. D., & Teasdale, G. M.
injury. Neuropsychology, 20, 675– 684. (1995). Neuropsychological consequences of two patterns of brain dam-
Schmitter-Edgecombe, M., Marks, W., Wright, M., & Ventura, M. (2004). age shown by MRI in survivors of severe head injury. Journals of
Retrieval inhibition in directed forgetting following severe closed-head Neurology, Neurosurgery, and Psychiatry, 59, 328 –331.
injury. Neuropsychology, 18, 104 –114. Zachary, R. A. (1991). Shipley Institute of Living Scale—Revised manual.
Schmitter-Edgecombe, M., & Woo, E. (2004). Memory self-awareness and Los Angeles: Western Psychological Services.
memory self-monitoring following severe closed-head injury. Brain
Injury, 18, 997–1016. Received June 26, 2006
Schneibel, R. S., & Levin, H. S. (1997). Frontal lobe dysfunction following Revision received October 4, 2006
closed head injury in children. In N. A. Krasnegor, G. R. Lyon, & P. S. Accepted December 11, 2006 䡲

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