NCT07404748

Brief Summary

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.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

First Submitted

Initial submission to the registry

December 19, 2025

Completed
2 months until next milestone

First Posted

Study publicly available on registry

February 11, 2026

Completed
5 days until next milestone

Study Start

First participant enrolled

February 16, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 31, 2026

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2026

Completed
Last Updated

April 8, 2026

Status Verified

April 1, 2026

Enrollment Period

1 month

First QC Date

December 19, 2025

Last Update Submit

April 7, 2026

Conditions

Keywords

PsychoeducationStress managementCoping skillsYoung adultsYouth mental health

Outcome Measures

Primary Outcomes (1)

  • Life Satisfaction Score (Satisfaction With Life Scale)

    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 Outcomes (1)

  • Perceived Stress Score (Perceived Stress Scale-14)

    Baseline and 4 weeks

Study Arms (4)

Control Group (No Stress Education, No Stress Task)

NO INTERVENTION

Participants in this group receive neither stress training nor stress tasks.

Stress Task Only (No Stress Education)

EXPERIMENTAL

Participants in this group receive stress-related tasks that do not involve stress training.

Behavioral: Stress Task

Stress Education Only (No Stress Task)

EXPERIMENTAL

Participants in this group receive stress training without any stressful tasks.

Behavioral: Stress Education

Stress Education + Stress Task

EXPERIMENTAL

Participants in this group receive both stress training and the task.

Behavioral: Stress EducationBehavioral: Stress Task

Interventions

A structured stress training program designed to increase participants' awareness of stress and teach them basic stress management and coping strategies.

Stress Education + Stress TaskStress Education Only (No Stress Task)
Stress TaskBEHAVIORAL

A stress task-based intervention that includes structured activities designed to engage participants and encourage active participation.

Stress Education + Stress TaskStress Task Only (No Stress Education)

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Erzincan Binali Yıldırım University

Erzincan, Merkez, 24100, Turkey (Türkiye)

Location

Study Officials

  • FEYZA KARSLI

    Erzincan Binali Yıldırım University, Department of Psychology

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
Not applicable. This is an open-label study with no masking.
Purpose
PREVENTION
Intervention Model
FACTORIAL
Model Details: This study employs a 2×2 factorial randomized design. Participants are randomly assigned to four groups based on the presence or absence of the intervention component and the presence or absence of the stress task. This design allows for the examination of the main and interaction effects of the intervention components.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

December 19, 2025

First Posted

February 11, 2026

Study Start

February 16, 2026

Primary Completion

March 31, 2026

Study Completion

April 1, 2026

Last Updated

April 8, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

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.

Locations