NCT07579767

Brief Summary

This study will test whether an 8-week multi-component positive psychology-based psychoeducation program can reduce perceived stress and improve psychological flexibility among first-year undergraduate nursing students. Eligible students who provide informed consent will be randomly assigned to either an intervention group or a waitlist control group. The intervention group will attend weekly 60-75 minute psychoeducation sessions including brief psychoeducation, experiential exercises, shared reflection, and home practice assignments. The waitlist control group will continue their usual routine during the study period and will not receive any intervention before post-test assessment. Outcomes will be assessed at baseline and immediately after the 8-week program using the Perceived Stress Scale-14 and the Acceptance and Action Questionnaire-II.

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
66

participants targeted

Target at P50-P75 for not_applicable

Timeline
3mo left

Started May 2026

Shorter than P25 for not_applicable

Status
not yet 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

Study Progress11%
May 2026Jul 2026

First Submitted

Initial submission to the registry

May 5, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

May 12, 2026

Completed
3 days until next milestone

Study Start

First participant enrolled

May 15, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2026

Last Updated

May 12, 2026

Status Verified

May 1, 2026

Enrollment Period

3 months

First QC Date

May 5, 2026

Last Update Submit

May 5, 2026

Conditions

Keywords

Positive PsychologyPsychoeducationPerceived StressPsychological FlexibilityUniversity Students

Outcome Measures

Primary Outcomes (1)

  • Change in Perceived Stress Scale-14 Total Score From Baseline to Post-intervention

    Perceived stress will be assessed using the Perceived Stress Scale-14. The scale consists of 14 self-report items scored on a 5-point Likert scale from 0 to 4. Total scores range from 0 to 56, with higher scores indicating higher perceived stress. Change will be evaluated from baseline to immediately after the 8-week intervention.

    Baseline and immediately after the 8-week intervention

Secondary Outcomes (1)

  • Change in Acceptance and Action Questionnaire-II Total Score From Baseline to Post-intervention

    Baseline and immediately after the 8-week intervention

Study Arms (2)

Positive Psychology Based Psychoeducation Program

EXPERIMENTAL

Participants in this arm will receive an 8-week multi-component positive psychology based psychoeducation program. Sessions will be delivered once weekly and will last approximately 60-75 minutes. Each session will include brief psychoeducation, experiential exercises, shared reflection, and home practice assignments.

Behavioral: Positive Psychology Based Psychoeducation Program

Waitlist Control

NO INTERVENTION

Participants in this arm will continue their usual routine during the 8-week study period and will not receive the psychoeducation program before post-test assessment. After post-test data collection is completed, they will be offered the psychoeducation program content as a booklet.

Interventions

The intervention is an 8-week multi-component positive psychology based psychoeducation program delivered once weekly in 60-75 minute sessions. The program includes psychoeducation and experiential practices related to gratitude, savoring, signature strengths, hope and goal-setting, meaning and values-based action, self-compassion, and maintenance of wellbeing practices. Each session includes brief psychoeducation, practice exercises, shared reflection, and a home practice assignment.

Positive Psychology Based Psychoeducation Program

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Being a first-year undergraduate student in the Department of Nursing at Harran University.
  • Volunteering to participate in the study and providing informed consent.
  • Having no reading, comprehension, or communication difficulty that would prevent completion of the data collection tools.
  • Being 18 years of age or older.

You may not qualify if:

  • Receiving regular psychotherapy or psychoeducation during the same academic period.
  • Having participated in a structured positive psychology-based psychoeducation or intervention program within the last 6 months.
  • Having a history of psychiatric hospitalization within the last 3 months or having an acute psychiatric crisis or instability that would make participation in the sessions inappropriate.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Stress, Psychological

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

Study Officials

  • Rabia Kaya, PhD

    Harran University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
Due to the nature of the psychoeducation intervention, participants and the researcher delivering the intervention cannot be blinded to group allocation. Outcomes will be assessed using self-report scales.
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Participants will be randomized in a 1:1 ratio to either the intervention group or the waitlist control group. The intervention group will receive the 8-week multi-component positive psychology based psychoeducation program, while the waitlist control group will continue their usual routine during the study period.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

May 5, 2026

First Posted

May 12, 2026

Study Start

May 15, 2026

Primary Completion (Estimated)

July 31, 2026

Study Completion (Estimated)

July 31, 2026

Last Updated

May 12, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be publicly shared because participants will be recruited from a single cohort of first-year nursing students, which may increase the risk of re-identification even after de-identification. Aggregate findings will be reported in scientific publications.