NCT07506694

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

87
On Track

Trial Health Score

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

Enrollment
90

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 15, 2022

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 16, 2022

Completed
3.5 years until next milestone

First Submitted

Initial submission to the registry

February 26, 2026

Completed
1 month until next milestone

First Posted

Study publicly available on registry

April 2, 2026

Completed
Last Updated

April 2, 2026

Status Verified

March 1, 2026

Enrollment Period

2 months

First QC Date

February 26, 2026

Last Update Submit

March 28, 2026

Conditions

Keywords

Nursing StudentsPsychoeducationCognitive Behavioral ApproachAnxietyDepressionStress

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

EXPERIMENTAL

Participants in this group received a group-based stress management psychoeducation program, designed to improve coping skills and reduce perceived stress levels, over seven sessions.

Behavioral: CBT-Based Stress Management Psychoeducation Program

Control Group

NO INTERVENTION

Participants 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.

CBT-Based Stress Management Psychoeducation Program

Eligibility Criteria

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

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

Study Sites (1)

Usak University, Faculty of Health Sciences

Uşak, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Anxiety DisordersDepression

Condition Hierarchy (Ancestors)

Mental DisordersBehavioral SymptomsBehavior

Study Officials

  • Saliha Esra ERYILMAZ AYDIN, PhD

    Usak University, Faculty of Health Sciences, Department of Nursing

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: This study was designed as a parallel group intervention study. Participants were assigned to either an intervention group receiving a psychoeducational program on stress management based on a cognitive behavioral approach, or a control group receiving no intervention. Both groups were evaluated at baseline, after the intervention period, and 3 months after the completion of the training, and the outcomes between the groups were compared.
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.

Locations