- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07404748
Stress Management and Life Satisfaction in University Students (USSMLS)
April 7, 2026 updated by: Feyza KARSLI, Erzincan Binali Yildirim Universitesi
The Effect of Stress Management Training on Perceived Stress and Life Satisfaction: An Experimental Mediation Analysis
This study aims to examine the effects of a structured psychoeducational program on the psychological well-being of university students.
Participants will be randomly assigned to either a psychoeducational group or a control group.
The psychoeducational program includes sessions designed to improve stress coping skills.
Data will be collected using self-report questionnaires administered after the intervention.
The study does not involve any drugs or medical devices and is considered to be of minimal risk.
The findings are expected to contribute to the development of effective psychosocial interventions for young adults.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
This study is designed to evaluate the relationship between coping with stress, perceived stress, and life satisfaction within a causal framework using an experimental mediating model.
The study examines the effect of structured stress coping training on participants' perceived stress and life satisfaction.
Psychoeducation is widely used in mental health settings to improve individuals' understanding of emotions, stress, and coping strategies.
However, evidence regarding its effectiveness in specific populations is limited.
Participants will be randomly assigned to either an intervention group receiving a psychoeducation program and performing a stress task, or a control group receiving no intervention and performing a stress task, for the duration of the study.
The psychoeducation program will be delivered in a group format and will focus on topics such as emotional awareness, stress management, adaptive coping skills, and problem-solving.
Data will be collected using self-report measures following completion of the intervention.
The study does not involve any pharmacological treatment or medical devices and is considered to be of minimal risk.
The results of this study are expected to shed light on future psychosocial intervention programs.
Study Type
Interventional
Enrollment (Estimated)
60
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
-
-
Merkez
-
Erzincan, Merkez, Turkey (Türkiye), 24100
- Erzincan Binali Yıldırım University
-
-
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:
- Being a university student
- Willingness to participate voluntarily in the study
- Attendance at all sessions throughout the education program
- No prior participation in a similar stress management or stress coping education program
Exclusion Criteria:
- Not being a university student
- Not providing voluntary consent to participate in the study
- Irregular attendance or non-completion of the education sessions
- Previous participation in a similar stress management or stress coping education 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: Prevention
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control Group (No Stress Education, No Stress Task)
Participants in this group receive neither stress training nor stress tasks.
|
|
|
Experimental: Stress Task Only (No Stress Education)
Participants in this group receive stress-related tasks that do not involve stress training.
|
A stress task-based intervention that includes structured activities designed to engage participants and encourage active participation.
|
|
Experimental: Stress Education Only (No Stress Task)
Participants in this group receive stress training without any stressful tasks.
|
A structured stress training program designed to increase participants' awareness of stress and teach them basic stress management and coping strategies.
|
|
Experimental: Stress Education + Stress Task
Participants in this group receive both stress training and the task.
|
A stress task-based intervention that includes structured activities designed to engage participants and encourage active participation.
A structured stress training program designed to increase participants' awareness of stress and teach them basic stress management and coping strategies.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Life Satisfaction Score (Satisfaction With Life Scale)
Time Frame: Baseline and 4 weeks
|
Life satisfaction was assessed using the Satisfaction With Life Scale (SWLS) developed by Diener et al. (1985), a validated self-report measure.
The scale consists of 5 items rated on a 7-point Likert scale, yielding total scores ranging from 5 to 35.
Higher scores indicate greater life satisfaction.
|
Baseline and 4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived Stress Score (Perceived Stress Scale-14)
Time Frame: Baseline and 4 weeks
|
Perceived stress was assessed using the Perceived Stress Scale-14 (PSS-14) developed by Cohen, Kamarck, and Mermelstein (1983), a validated self-report questionnaire designed to measure the degree to which situations in one's life are appraised as stressful.
The scale consists of 14 items rated on a 5-point Likert scale ranging from 0 (never) to 4 (very often).
Total scores range from 0 to 56, with higher scores indicating greater perceived stress.
Seven positively stated items are reverse scored.
|
Baseline and 4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: FEYZA KARSLI, Erzincan Binali Yıldırım University, Department of Psychology
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)
February 16, 2026
Primary Completion (Actual)
March 31, 2026
Study Completion (Estimated)
April 1, 2026
Study Registration Dates
First Submitted
December 19, 2025
First Submitted That Met QC Criteria
February 8, 2026
First Posted (Actual)
February 11, 2026
Study Record Updates
Last Update Posted (Actual)
April 8, 2026
Last Update Submitted That Met QC Criteria
April 7, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- Protocol No: 11/03
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Individual participant data will not be shared due to ethical and confidentiality considerations, as the study involves sensitive psychological information and participants did not provide consent for data sharing.
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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