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DIABETICMedicine

DOI: 10.1111/dme.14078

Short Report: Educational and Psychological Aspects


A pilot randomized controlled trial of a gratitude
intervention for adolescents with Type 1 diabetes

K. R. Schache1, P. L. Hofman2 and A. S. Serlachius1


1
Department of Psychological Medicine, and 2Liggins Institute, University of Auckland, Auckland, New Zealand

Accepted 13 July 2019

Abstract
Aim Cost-effective psychosocial interventions that can feasibly be implemented into busy clinical settings are needed to
improve psychological and physical health outcomes in adolescents with Type 1 diabetes. We examined the efficacy of a
gratitude journalling intervention to improve psychological well-being and glycaemic control in adolescents aged 10–16
years with Type 1 diabetes.
Methods Eighty adolescents were randomized to the 8-week gratitude intervention (N = 40) or standard care
(N = 40). Self-reported measures of stress, quality of life, self-care, depression and gratitude were assessed at baseline
and 8 weeks after baseline. Glycaemic control (HbA1c) was assessed at baseline and 12 weeks after baseline. A per-
protocol analysis was conducted with the adolescents who completed all questionnaires (N = 60). Analysis of covariance
(ANCOVA) was used to examine differences between treatment arms at follow-up adjusting for baseline scores.
Results There was no evidence of any between-group differences in the psychological or behavioural measures at follow-up
(all P-values > 0.05). Glycaemic control slightly increased in the control group while remaining stable in the gratitude group,
with a between-group difference of 6.1 mmol/mol [95% confidence interval (CI) 2.6 to 14.7; 0.6%, 95% CI 0.2 to 1.3] at
12 weeks after baseline. After adjusting for baseline HbA1c, this between-group difference was significant (P = 0.048).
Conclusions This is the first randomized trial of a gratitude journalling intervention for adolescents with Type 1
diabetes. Gratitude journalling interventions represent a clinically usable approach. If and how it helps to stabilise
glycaemic control in adolescents with Type 1 diabetes remains to be confirmed in future research.
Diabet. Med. 00, 1–5 (2019)

on their efficacy for influencing physiological health outcomes


Introduction
[10]. Gratitude interventions come in different formats with the
Adolescents with Type 1 diabetes are at a high risk for most common being a gratitude journal [8], where participants
psychiatric disorders and suboptimal glycaemic control as they are asked to write a list of things for which they are thankful; the
navigate a new developmental period while managing a chronic format also used in the current study. Our objective was to
illness [1,2]. Reviews and meta-analyses of psychosocial examine the efficacy of a gratitude journalling intervention for
interventions for adolescents with Type 1 diabetes have adolescents with Type 1 diabetes. We hypothesized that the
demonstrated efficacy in improving psychological well-being, gratitude intervention would improve psychological well-being
but improvements are often harder to achieve for glycaemic and glycaemic control in comparison with standard care.
control [2,3]. There is also a lack of studies that are cost-
effective and can realistically be integrated into clinical care
Research design and methods
[4,5]. A promising approach may be gratitude interventions.
Observational studies in healthy populations have found a A pilot randomized controlled trial (RCT) of an 8-week
consistent association between highgratitude and lower rates of gratitude journalling intervention (treatment group) was
depression and stress [6,7]. Gratitude interventions have compared with standard care (control group) in 80 adolescents
demonstrated improvements in psychological well-being in with Type 1 diabetes between March and June 2017. Ethical
healthy adolescent populations [8,9] and research is emerging approval was granted by the Health and Disability Ethics
Committee and all participants provided written informed
consent. CONSORT guidelines were followed and the trial
Correspondence to: Anna Serlachius. E-mail: a.serlachius@auckland.ac.nz

ª 2019 Diabetes UK 1
DIABETICMedicine Gratitude intervention in adolescents with Type 1 diabetes  K. R. Schache et al.

and at their next clinic visit 12 weeks after baseline (window


What’s new? of 12–16 weeks after baseline). Other covariates which were
• There is a growing need for clinically usable interven- assessed included sex, age, ethnicity, comorbidities, insulin
tions to improve psychological well-being in adoles- regimen and date of diagnosis.
cents with Type 1 diabetes. After completing baseline questionnaires, participants
were randomized into the treatment group (gratitude inter-
• Gratitude journalling interventions are a novel vention) or the control group (standard care). The treatment
approach for improving psychological and physical group was provided with a journal and based on previous
health outcomes in adolescents. gratitude interventions [8] were asked to write down three
• We found no evidence to suggest that the gratitude things they were grateful for every day for 8 weeks. The
intervention improved psychological outcomes in ado- heading on each page of the journal read ‘Today I am
lescents with Type 1 diabetes. thankful for:’ and had three lines underneath for adolescents
to write down anything they wanted. Additionally, the pages
• The gratitude journalling intervention may help to were labelled with each day of the week, serving as a cue to
stabilize glycaemic control in adolescents with Type 1 action. Participants were also told that the journals were
diabetes compared with standard care. confidential and they would not be collected at the end of the
• Further research is needed to clarify whether gratitude study. During the 8-week trial, no additional reminders were
journalling interventions are a useful approach to provided.
improve health outcomes in this population. Eight weeks after baseline, both groups were asked to
complete the same set of questionnaires. At the follow-up
assessment, an additional question was added to the treat-
was registered with the Australian New Zealand Clinical ment group’s questionnaires to assess adherence to the
Trials Registry (ANZCTR) (ACTRN12617000248369). journal (daily/almost every day/two or three times a week/
once a week or less).
Participants and randomization

Participants were recruited from three paediatric and ado- Statistical analyses
lescent diabetes clinics in Auckland, New Zealand. Inclusion The sample size was based on a hypothesized difference in
criteria included being 10–16 years old and diagnosed with stress levels (primary outcome) at follow-up between the two
Type 1 diabetes for > 6 months. Exclusion criteria included groups using an independent samples t-test (one-tailed) with
non-English-speaking adolescents and adolescents diagnosed 80% power and a significance level of 0.05. For the power
with serious developmental or psychiatric disorders requiring calculation, we used an effect size from a stress management
ongoing treatment. During recruitment 150 adolescents were intervention for youth [16], which found a large effect in
approached, of which 80 consented to participate and were stress levels between groups (Cohen’s d =0.6). A minimum of
randomized. The most common reason for non-participation 72 participants were required, which was increased to 80 to
was lack of time to participate in research. Treatment allow for attrition.
allocations were computer generated by a biostatistician Eleven participants from the control group and nine
independent of the intervention delivery and participants from the treatment group were lost to follow-up and did
were randomized using sequentially numbered sealed opaque not complete their post-intervention questionnaires.
envelopes. Because of the high attrition, a per-protocol analysis was
conducted, in which the 20 participants who were lost to
follow-up were not included (N = 60). For HbA1c, there
Measures and intervention
were two missing values at follow-up, which we treated as
At baseline, participants completed the following self-report missing data. Data were tested for violations of statistical
questionnaires: Diabetes Stress Questionnaire for Youths assumptions. Analysis of covariance (ANCOVA) was used
(higher scores indicate higher stress) [11], the Centre for to examine differences between groups at follow-up
Epidemiological Studies Depression Scale for Children adjusting for baseline scores. Means, standard deviations
(higher scores indicate higher levels of depressive symptoms) (SD) and 95% confidence intervals (CI) are presented with
[12], the ‘Impact of Diabetes’ subscale from the Diabetes the analyses.
Quality of Life for Youths scale (higher scores indicate worse
quality of life) [13], the Self-Care Inventory-Revised Version
Results
(higher scores indicate more optimal self-care behaviours)
[14] and the Gratitude Questionnaire-6 (higher scores The baseline characteristics of the two treatment arms
indicate greater levels of gratitude) [15]. Glycaemic control (N = 60) as well as the group lost to follow-up (N = 20)
(HbA1c) was also measured as part of their routine clinic visit are presented in Table S1.

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Short Report DIABETICMedicine

Per-protocol Between-group differences at follow-up (per protocol)

The baseline demographic and clinical characteristics were Table 1 depicts the mean differences in outcome measures
similar between the treatment and control groups. The between the groups at baseline and 8 weeks after baseline (12
mean age for the total sample (N = 60) was 12.2 years (SD weeks after baseline for HbA1c). As reflected in the mean
1.8) and there were 32 girls (53.3%). The majority of the differences and 95% CIs, there was no evidence of any group
sample identified as New Zealand European (N = 39, differences in stress, quality of life, self-care behaviours,
65%), with eight participants (13.3%) identifying as Maori depression or gratitude. For HbA1c there was a between-
(indigenous New Zealanders), four as Pasifika (6.7%) and group difference of 6.1 mmol/mol (95% CI 2.6 to 14.7;
nine (15%) as other ethnic groups. The baseline HbA1c for 0.6%, 95% CI 0.2 to 1.3) at 12 weeks after baseline.
the total sample was 69 mmol/mol (SD 12.2) (8.4%, SD 1.1). Lastly, ANCOVAs were also conducted to examine group
Thirty-three participants (55%) were on multiple daily differences at follow-up while adjusting for baseline scores.
injections and 27 participants (45%) were on pump The results of the ANCOVA mostly supported the above
therapy. findings. The effect of the gratitude journalling intervention
on HbA1c was statistically significant after adjusting for
baseline scores, F(1, 56) = 4.08, P = 0.048. Figure 1
Lost to follow-up demonstrates that while HbA1c remained stable during the
The adolescents who were lost to follow-up had a higher 12 weeks in the gratitude group, HbA1c increased in the
baseline HbA1c (78 mmol/mol, SD 18.4; 9.3%, SD 1.7), higher control group.
levels of stress, worse quality of life, and reported lower self-
care behaviours than the participants who completed the Supplementary analyses
intervention (see Table S1). Although underpowered, subgroup analyses were carried out
to explore whether the lack of between-group differences in
the psychological measures at follow-up might be due to a
Self-reported adherence to the gratitude intervention
ceiling effect (e.g. the GQ-6 has a range between 7 and 42
Forty-five per cent of adolescents in the treatment group and both groups scored > 30 at baseline) or due to non-
reported writing in their gratitude journal every day or adherence to the intervention. No between-group differences
almost every day. An additional 26% reported using it two were found at follow-up between the participants in the
or three times per week and 29% once a week or less during intervention group who had lower/suboptimal scores on the
the 8-week trial period. psychosocial outcomes at baseline (e.g. using the cut-off for

Table 1 Mean differences in outcome measures at baseline and follow-up (per protocol analysis)

Measures Gratitude N = 31) Control N = 29) Mean difference 95% CI) P-value*

Stress
Baseline 32.8 (8.8) 34.3 (7.8) 1.5 ( 2.8 to 5.8)
8 weeks 31.2 (8.5) 32.5 (8.2) 1.3 ( 3.0 to 5.6) 0.999
Impact of diabetes
Baseline 47.0 (12.5) 48.7 (10.6) 1.6 ( 4.4 to 7.6)
8 weeks 48.2 (13.1) 48.5 (10.2) 0.3 ( 5.8 to 6.4) 0.585
Self-care
Baseline 58.4 (7.6) 57.8 (8.2) 0.6 ( 4.7 to 3.5)
8 weeks 59.3 (5.7) 58.2 (8.2) 1.1 ( 4.7 to 2.6) 0.591
Depression
Baseline 14.9 (12.6) 14.1 (10.7) 0.7 ( 6.8 to 5.3)
8 weeks 13.9 (12.7) 12.2 (7.9) 1.7 ( 7.2 to 3.8) 0.600
Gratitude
Baseline 35.5 (6.6) 34.1 (5.1) 1.4 ( 4.5 to 1.7)
8 weeks 36.3 (6.7) 36.0 (4.4) 0.3 ( 3.2 to 2.7) 0.530
HbA1c
Baseline (mmol/mol) 69 (10.9) 68 (13.7) 0.3 ( 6.6 to 6.1)
Baseline (%) 8.4 (1.0) 8.4 (1.3) 0.02 ( 0.6 to 0.6)
12 weeks (mmol/mol) 68 (10.7) 74 (21.0) 6.1 ( 2.6 to 14.7)
12 weeks (%) 8.3 (1.0) 8.9 (1.9) 0.6 ( 0.2 to 1.3) 0.048*

P-values refer to analysis of covariance (ANCOVA) for between-group comparisons at follow-up. Data are unadjusted means (SD).
*P < 0.05. ANCOVAs adjusting for baseline scores.

ª 2019 Diabetes UK 3
DIABETICMedicine Gratitude intervention in adolescents with Type 1 diabetes  K. R. Schache et al.

90 intervention. There are a few possible reasons for why self-


reported gratitude did not improve in the treatment group,
including that gratitude scores at baseline were relatively high
HbA1c (mmol/mol)

80
in both groups, indicating that a ceiling effect may have
occurred, although our supplementary analyses did not sup-
70 port this theory. Another likelihood for the lack of improve-
ments in psychological outcomes include both the high
attrition (N = 20) and relatively high non-adherence to the
60
gratitude intervention (> 50% of adolescents allocated to the
treatment group did not write in their gratitude journal every
50 day), therefore diluting the effects of the intervention and
Baseline 12 weeks post-intervention
decreasing power. Notably, in our supplementary analyses,
FIGURE 1 Change in HbA1c from baseline to 12 weeks after baseline the more adherent adolescents demonstrated significantly
for the per protocol analysis (N = 60). Means at 12 weeks are adjusted lower HbA1c at follow-up compared with those who were
for baseline HbA1c. Error bars represent 95% confidence intervals. less adherent, but there were no group differences in the
Solid line, gratitude group; dashed line, control group. psychological measures. This provides further evidence that
the gratitude journaling intervention may help to stabilize
the depression scale or dichotomizing gratitude) and the HbA1c, but the mechanisms remain unknown. Finally, the
control group (all P > 0.05). Similarly, no differences were adolescents who were lost to follow-up had higher HbA1c
found at follow-up when we compared participants who and reported higher stress and worse quality of life, indicat-
adhered to the gratitude journal (wrote in the journal daily/ ing that they may have had the most scope to improve. It is
almost daily, N = 14) and the control group (all P > 0.05). well known that adolescents are a notably hard-to-reach
Lastly, we also compared the adherent participants (N = 14) group and adolescents with Type 1 diabetes are already
with those who wrote in the gratitude journal less regularly overburdened with diabetes-related tasks. Therefore, devel-
(N = 16) in the intervention group only. Although no between- oping psychosocial interventions that are feasible and appeal
group differences were found in the psychological measures at to this population remains an important goal for future
baseline or 3 months, a group difference was observed for research.
HbA1c at follow-up after adjusting for baseline scores, F(1, Strengths of this study include its clinical utility. Many
27) = 4.24, P = 0.049, with the more adherent group demon- psychological interventions for people living with chronic
strating lower HbA1c. Although underpowered, these findings disease are not translated well or translatable at all into a
suggest that those participants who adhered to the gratitude clinical setting [5]. Limitations of this study include its short-
intervention had a greater improvement in HbA1c compared term follow-up, high levels of attrition and relatively high
with those who were less adherent, with a between-group levels of non-adherence to the journalling intervention. We
difference of 9.2 mmol/mol (95% CI 16.6 to 1.9; 0.8%, also did not have an active control group. We plan to follow-
95% CI 1.5 to 0.2) at 12 weeks after baseline. up this cohort of adolescents to examine if these results are
maintained. Future research is required to confirm these
findings in a larger sample with an active control group and
Conclusions
to examine the underlying pathways through which gratitude
This is the first RCT of a gratitude journaling intervention for may be influencing glycaemic control.
adolescents with Type 1 diabetes. The results did not support
our hypotheses that a gratitude intervention would improve
Funding sources
psychological well-being in adolescents with Type 1 diabetes
compared with standard care; however, the findings did None.
suggest that a gratitude intervention may have the potential
to stabilize glycaemic control in adolescents with Type 1
Competing interest
diabetes. Gratitude interventions may influence health out-
comes via an increase in healthy behaviours (e.g. improved None declared.
diet) [17] or through biological functioning (e.g. inflammation,
blood pressure) [18,19]. Changes in HbA1c due to a psycho-
Ethical approval
logical intervention alone are difficult to achieve [3] and so this
pilot study provides a basis for future research into this area. The study was approved by the Health and Disability Ethics
Unexpectedly we did not see any changes in the psycholog- Committee [Auckland, New Zealand], and informed consent
ical or behavioural measures, including self-care behaviours or was obtained from all participants. This research study was
gratitude, which makes it difficult to ascertain that the conducted in accordance with the guidelines of the Declara-
between-group differences in HbA1c were due to the gratitude tion of Helsinki

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Short Report DIABETICMedicine

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