Professional Documents
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DOC-20240710-WA0017.
DOC-20240710-WA0017.
• Validation refers to whether or not that the test measures what it was designed
to measure.
• The validity of the instruments for data collection for our study will be done
through expert judgement, face validity and pilot testing.
• Face validity is the assessment of whether an instrument appears on its face to
measure what its intended to measure.
• Pilot study will be done and any correction found will be made accordingly in
relation to the study topic. The results of the pilot study will not be included in
the final findings of the research.
• For expert judgement, three or more lecturers should revies the instrument and
agree if its appropriate for a particular situation.
• A research that uses an instrument that is not validated is usually met with
suspicion (Fowler, 2009).
Data Management, Analysis and
Presentation
• Procedure for data management and storage
Data collected will be recorded into Google sheets 2021 and used to examine the
variables under study.
The whole data under the management of the researcher will be stored, managed
and applied.
For the electronic data, the data will be stored in an encrypted form with access
only to the researchers.
The hard data will be stored in the nursing library for a few years before it being
destroyed.
Procedure for Data Analysis and
Presentation
• Raw data gathered will be recorded in a google sheet. We will check for any
missing values, outliers or inconsistencies and clean the dataset ensuring data
integrity.
• Data will be coded then transported to an efficient statistical tool for accurate
analysis.
• The results obtained will be presented in various forms including tables, graphs,
charts and measures of central tendency.
Ethical Consideration
• Are a set of principles that guide the research designs and practices.
• This study will consider ethical issues into account.
• These will include : Obtaining an informed consent, information confidentiality,
voluntary participation, anonymity, right to withdraw, physical or psychological
harm and deception and debriefing.
• We will seek permission from the Dean of Students regarding approval of the
study.
• The informed consent will be appropriately documented.
• I will give the participants a document explaining to them what will be needed of
them and the potential risks.
• The participants are not forced to participate in research if the study brings harm
to them
Expected Findings and Relevance to
Knowledge