Clinical Trial

Feasibility of SOLAR Group Program Among MHPSS Workers After the Earthquake

Active, Not Recruiting
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Record status
This record was last updated March 24, 2025 (before its estimated September 2025 completion). Its status may not reflect the trial's current state.
Summary
The goal of this intervention program is to provide the feasibility of a culturally adapted version of the SOLAR program among mental health and psychosocial support (MHPSS) workers who provide psychological or psychosocial support to the survivors of the earthquakes on February 6, 2023, in Türkiye. The main questions it aims to answer are: 1. Will the SOLAR Group Program reduce psychological distress at the post-test and follow-up compared to the pre-test? 2. Will the SOLAR Group Program reduce secondary traumatic stress at the post-test and follow-up compared to the pre-test? 3. Will the SOLAR Group Program reduce anxiety and depressive symptoms at the post-test and follow-up compared to pre-test? Participants will be asked to sign a consent form. Upon accepting it, they will fill out: * a demographic form, * the Kessler Psychological Distress Scale (K10), * Assessment of Suicidal Thoughts for the screening. Before the SOLAR intervention program, participants will be asked to complete: * the Secondary Traumatic Stress Scale (STSS), * Generalized Anxiety Disorder-7 (GAD-7), * the Patient Health Questionnaire (PHQ-9) if they approve participation in these surveys. After collecting their pre-test scores, they will receive the SOLAR intervention program. During the program, they will be asked to participate in each session, lasting 5 weeks. After the program, they will be asked to participate process evaluation interview.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-01-22.
Status change: Not Yet Recruiting → Active, Not Recruiting 2025-03-20
Trial Details
NCT Number NCT06231927
Lead Sponsor Koç University
Conditions Psychological Distress, Secondary Trauma, Depression, Anxiety
Enrollment 20 participants
Start Date 2024-04-15
Primary Completion 2025-09 (estimated)
Study Completion 2025-10 (estimated)
Updated on ClinicalTrials.gov 2025-03-24