Effect of a Cognitive Behavioral Stress Management Psychoeducation Program in Nursing Students
SYPP
The Effect of a Cognitive-Behavioral Approach-Based Stress Management Psychoeducation Program on Depressive, Anxiety, and Stress Symptom Levels in Nursing Students
1 other identifier
interventional
90
1 country
1
Brief Summary
This study aimed to evaluate the effect of a cognitive-behavioral approach-based stress management psychoeducation program on the depression, anxiety, and stress levels of nursing students. The study was conducted with undergraduate nursing students studying at the Faculty of Health Sciences of a university. Students in the experimental group received a structured stress management psychoeducation program based on the cognitive-behavioral approach. The control group received no intervention. Data were collected three times using self-report questionnaires: before, after, and three months after the intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2022
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 15, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 15, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
August 16, 2022
CompletedFirst Submitted
Initial submission to the registry
February 26, 2026
CompletedFirst Posted
Study publicly available on registry
April 2, 2026
CompletedApril 2, 2026
March 1, 2026
2 months
February 26, 2026
March 28, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Depression, Anxiety, and Stress Levels
Changes in depression, anxiety, and stress levels were assessed using the Depression Anxiety Stress Scale-21 (DASS-21). The items on the scale are designed to assess how individuals have felt in the past week, and participants are asked to read these statements and rate the frequency of negative emotions. This 21-item scale uses a 4-point Likert scale (0=never-3=always) and consists of 7 questions each measuring the dimensions of depression, anxiety, and stress. A score of 5 or higher on the depression subscale, 4 or higher on the anxiety subscale, and 8 or higher on the stress subscale indicates that the individual has the relevant problem.
Baseline (pre-intervention), immediately after the intervention, and 3-month follow-up
Study Arms (2)
CBT-Based Stress Management Psychoeducation Program
EXPERIMENTALParticipants in this group received a group-based stress management psychoeducation program, designed to improve coping skills and reduce perceived stress levels, over seven sessions.
Control Group
NO INTERVENTIONParticipants in this arm did not receive the psychoeducation program during the study period and were placed on a wait-list.
Interventions
The intervention implemented consisted of a structured psycho-educational program based on the principles of cognitive behavioral therapy. The program was conducted in group sessions and aimed to improve stress coping skills and reduce levels of depression, anxiety, and stress.
Eligibility Criteria
You may qualify if:
- Scoring between 10 and 29 on the Beck Depression Inventory (BDI) during the initial assessment
- Being between 18 and 25 years of age
- Not having received any prior psychiatric diagnosis or treatment
- Not having received prior stress management training
- Volunteering to participate in the study
You may not qualify if:
- Scoring outside the 10-29 range on the BDS
- Being under 18 or over 25 years of age
- Having a history of psychiatric diagnosis or treatment
- Having received stress management training
- Refusing to participate in the study
- Not having attended more than three sessions
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Uşak Universitylead
Study Sites (1)
Usak University, Faculty of Health Sciences
Uşak, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Saliha Esra ERYILMAZ AYDIN, PhD
Usak University, Faculty of Health Sciences, Department of Nursing
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 26, 2026
First Posted
April 2, 2026
Study Start
March 15, 2022
Primary Completion
May 15, 2022
Study Completion
August 16, 2022
Last Updated
April 2, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be made publicly available due to ethical restrictions, as the study involves sensitive psychological data and participant consent did not cover data sharing beyond the research team.