- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07424131
The Effect of Theory-based Education on Cultural Sensitivity and Compassion
April 21, 2026 updated by: Sakarya University
The Effect of Theory-based Education on Cultural Sensitivity and Compassion Levels in Nursing Students
Strengthening cultural sensitivity and compassion plays a critical role in reducing health inequalities, especially for vulnerable and disadvantaged groups.
This study is designed to determine the effect of an educational program based on the Theory of Planned Behavior on the cultural sensitivity and compassion levels of nursing students.
The study, planned as a parallel-group, single-blind, randomized pre-test-post-test controlled experimental design, will include a total of 80 students, with 40 students in each group.
The intervention group will receive an educational program based on the Theory of Planned Behavior, in modules over four weeks.
Data will be analyzed using IBM SPSS Statistics for Windows, version 27.0 (IBM Corp, Armonk, NY, USA).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
80
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Adapazarı
-
Sakarya, Adapazarı, Turkey (Türkiye), 54000
- Sakarya Provincial Directorate of Health
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Students studying in the nursing department of a university,
- Who volunteer to participate in the study,
- Who were born in Turkey or have lived in Turkey for at least one year,
- Who have no difficulty speaking and understanding Turkish and have started clinical internships.
Exclusion Criteria:
- Students who did not give their consent at any stage of the study and withdrew,
- Those who have serious difficulties in speaking and understanding Turkish,
- Those who have previously participated in a similar training program.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
|
The intervention group will receive a training program based on the Theory of Planned Behavior, consisting of 4-week modules.
|
|
No Intervention: Control
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cultural Sensitivity Scale for Nursing Students
Time Frame: Four Weeks
|
The 15-item scale is a 6-point Likert type.
The scale has 4 sub-dimensions: (1) Patient and healthcare professional behavior, (2) Self-assessment, (3) Self-awareness, and (4) Cultural influence.
The lowest possible score on the scale is 15, and the highest possible score is 90.
As the score on the scale increases, the level of cultural sensitivity also increases.
|
Four Weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Compassion Scale
Time Frame: Four Weeks
|
The scale consists of 24 items in total and six sub-dimensions: "Compassion, Indifference, Awareness of Sharing, Detachment, Mindfulness, and Disengagement."
The scale is a 5-point Likert type.
The total score ranges from 24 to 120, with higher scores indicating increased levels of compassion.
|
Four Weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 6, 2025
Primary Completion (Actual)
October 31, 2025
Study Completion (Actual)
March 4, 2026
Study Registration Dates
First Submitted
February 13, 2026
First Submitted That Met QC Criteria
February 13, 2026
First Posted (Actual)
February 20, 2026
Study Record Updates
Last Update Posted (Actual)
April 22, 2026
Last Update Submitted That Met QC Criteria
April 21, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 81829502.903/2
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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