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Clinical Trials/NCT07357129
NCT07357129Not yet recruitingNot Applicable

A Psychosocial Intervention Program to Improve Stress Management Among Young Women: A Pilot Study

Bogazici University0 sites60 target enrollmentStarted: January 15, 2026Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
60
Primary Endpoint
K10

Study Overview

Brief Summary

This pilot study aims to evaluate the feasibility and probable impact of a low intensity psychosocial intervention program designed to help individuals to manage their stress levels. Consequently, this study will implement and measure the feasibility, randomization, retention, assessment procedures, and preliminary effects of the Self-Help Plus (SH+) program developed by the World Health Organization. This intervention, which has been used among immigrants and has proven to be effective, is intended to be implemented for the first time among distressed young Turkish-speaking women in Türkiye (ages between 18 and 29). Participants who will receive this intervention program will be compared with others in the control group who experience similar stress levels but will not receive SH+ during the trial period. Participants in the control group will receive SH+ after the completion of follow-up assessments at 3 months.

Detailed Description

This pilot study aims to evaluate the feasibility, acceptability, appropriateness, and probable effectiveness of a community-based stress management program, designed to reduce the stress levels and improve psychological well-being.

Stress is part of daily life; ability to effectively cope with stress plays a crucial role in both physical health and psychological well-being. Numerous studies have shown that effective stress management is a protective factor for physical and psychological well-being. The positive effects of stress coping skills are not limited to reducing current psychological distress; they also act as protective skills, preparing individuals for future stressors. Globally and in Türkiye, the rate of psychiatric disorders is higher among women than men. Major depression and anxiety disorders, the most common disorders around the globe, are twice as common in women as in men.

Consequently, this study aims to implement and measure the feasibility of the Self-Help Plus (SH+) program developed by the World Health Organization in the Turkish context. This intervention, which has been used among immigrants and has proven to be effective, is intended to be implemented for the first time among distressed Turkish-speaking women in Türkiye. The primary goal of the proposed pilot study is to measure its feasibility and probable effectiveness, in order to design a fully powered RCT.

The study will be conducted in Istanbul, Türkiye. Participants will be recruited through social media outlets and via snowballing. Once required number of participants who meet inclusion criteria (distressed without suicide risk) is reached (total of 60 participants), they will be randomly assigned to intervention and control groups (randomization to two arms according to 1:1 principle using an online randomization software). 30 randomly allocated participants will be divided into two groups, and will receive five sessions of SH+ (sessions are weekly, last about 90 to 120 minutes). The remaining 30 participants will be on a waitlist, and will receive the program once follow up assessments are completed. All participants will complete primary and secondary outcome measures at three time points: baseline, within one week upon completion of 5 week sessions (post assessment), and 3 months after the completion of 5 week sessions (follow-up assessment).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 29 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • being a woman
  • being ages between 18 and 29
  • being fluent in Turkish
  • having high levels of psychological distress (scoring above 15 on the Turkish version of the Kessler Psychological Distress Scale (K-10)

Exclusion Criteria

  • having an imminent risk of suicide (measured by WHO PM+ assessment tool)
  • having a diagnosis for severe mental disorder (e.g., psychotic disorders or substance dependence)
  • having cognitive impairment (e.g., received a diagnosis of dementia or severe intellectual disability)
  • currently receiving psychological treatment, e.g., therapy.

Arms & Interventions

Self-Help Plus Intervention Group

Experimental

This arm will receieve Self-Help Plus (SH+) intervention, which is a five-session stress management program developed by the World Health Organization (WHO). The program is designed to be administered in a group format for maximum of 30 participants. Facilitators are not required to be mental health professionals. The best way to implement the program is to train non-specialists from the local communities where it will be delivered. These community members may become facilitators following a brief training. The program is composed of listening to pre-recorded audios along with some group discussions moderated by the facilitators.

Intervention: Self-Help Plus (Behavioral)

Control Group

No Intervention

Participants in this no intervention group will serve as the control group. Upon the completion of the study (after 3 months follow-up assessments), participants in this group will also receive the same intervention to ensure ethical considerations and promote equity.

Outcomes

Primary Outcomes

K10

Time Frame: Baseline, within one week after the completion of 5 sessions, and 3 months after the completion of 5 sessions

Kessler Psychological Distress Scale (K10) is a 10-item questionnaire that aims to measure psychological distress symptoms. Each of the 10 items are scored on a scale of 5 points (1 = "none of the time" to 5= "all of the time"), providing a total score between 10 and 50. Higher scores indicate higher levels of psychological distress. A Turkish version is available and will be used in the current study.

Secondary Outcomes

  • Patient Health Questionnaire-9 (PHQ-9)(Baseline, within one week of completion of 5 sessions, and 3 months after the completion of 5 sessions)
  • General Anxiety Disorder-7 (GAD-7)(Baseline, within one week upon completion of 5 sessions, and 3 months after completion of 5 sessions)
  • World Health Organization-Five Well-Being Index (WHO-5)(Baseline, within one week upon completion of 5 sessions, and 3 months after completion of 5 sessions)
  • General Self Efficacy Scale (GSES)(Baseline, within one week upon completion of 5 sessions, and 3 months after 5 sessions)

Investigators

Sponsor
Bogazici University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Yasemin Sohtorik İlkmen

Assistant Professor

Bogazici University

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