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Completed

NCT Number: NCT06189937

Group CA-CBT Intervention to Reduce Psychological Distress of Earthquake Survivors

Earthquakes in Türkiye cause survivors to develop serious and prolonged mental health issues and adapted versions of cognitive behavioral therapy has proven to be successful in addressing these concerns.The main goal of this pilot randomized control trial (RCT) is to test potential effectiveness of Culturally Adapted Cognitive Behavioral Therapy (CA-CBT) in reducing psychological distress and depressive symptoms and increasing well-being of earthquake survivors.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Koc University

Istanbul, Turkey (Türkiye)

About this study

Türkiye was struck by two large earthquakes with moment magnitudes 7.7. and 7.6, on the 6th of February 2023. The disaster resulted in more than 50 thousand people losing their lives, more than 107 thousand people getting injured and more than 84 thousand buildings being demolished, severely damaged or slated for demolition. After the earthquakes, various mental health issues can emerge among the survivors such as depression, anxiety disorders, posttraumatic stress disorder, sleep problems, prolonged grief disorder, decrease in quality of life, increase in suicidality and substance use, and their effects can be prolonged if not treated.

An effective treatment method for the mental health issues that the earthquake survivors may experience is cognitive behavioral therapy (CBT) which is effective both in individual and group formats. Moreover, culturally adapted versions of CBT demonstrated higher effectiveness. One such adaptation, developed as a transdiagnostic intervention by Devon Hinton, is known as Culturally Adapted CBT (CA-CBT), which has shown effectiveness across various cultures and countries. It has been successfully applied to depressed and traumatized women in Türkiye, reducing depressive symptoms and PTSD. CA-CBT incorporates emotion regulation techniques, mindfulness and stretching exercises as well as cognitive-behavioral approach principles. Some advantages of the CA-CBT are: (1) as a transdiagnostic intervention, it can be applied to treat various psychopathologies (2) as a group intervention, it can be applied to multiple individuals simultaneously, (3) as an 8-session intervention, it can improve mental health in the short term.

CA-CBT has not been tested with a population specifically consisting of individuals affected by earthquakes before. This pilot randomized control trial (RCT) aims to assess the potential effectiveness and feasibility of CA-CBT, specifically tailored for the earthquake survivors, and their mental health issues following the disaster. The main research questions of the study are whether the group CA-CBT is effective in decreasing psychological distress and depressive symptoms and increasing well-being among earthquake survivors one month after post-assessment.

The study is planned to be conducted with the collaboration with non-governmental organizations giving services to earthquake survivors. After the baseline assessment, eligible 60 participants will be randomized to two arms according to the 1:1 principle with automatized randomization software. 30 randomly allocated participants will receive CA-CBT and 30 randomly allocated participants will receive Enhanced Care as Usual (E-CAU) as the control group. One week after the completion of the sessions, all participants including control group participants will have post-assessments consisting of the same questionnaires as baseline assessment. One month after the post-assessment, all participants including control group participants will have follow-up assessments consisting of the same questionnaires as baseline and post-assessments.

If CA-CBT proves effective for individuals affected by earthquakes, it can be disseminated among mental health care professionals. Consequently, more earthquake survivors can access this high-quality evidence-based intervention adapted to their culture.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Being 18 years old or older.
  • Having experienced the earthquake.
  • Having a considerable amount of psychological distress: scoring 16 or higher on the Kessler Psychological Distress Scale (K10).

Exclusion criteria

  • Having a severe mental disorder (conducted by a trained assessor).
  • Presenting suicidality (assessed by the Problem Management Plus Suicidality Tool).

Treatment and study plan

Culturally Adapted Cognitive Behavioral Therapy (Ca-CBT)

Behavioral

In this study, an 8- session (90 to 120 minutes) group version of the transdiagnostic intervention CA-CBT tailored for earthquake survivors will be applied.

Contents of the sessions are:

  • Education on psychological trauma and its treatment, and basics of emotion regulation techniques
  • Education on anxiety and depressive disorders and their treatment
  • Muscle relaxation and stretching exercises
  • Education about depressive and grief-related disorders and disturbing memories protocol
  • Interoceptive exposure: head rotation and hyperventilation
  • Anxiety, worry, and stress
  • Anger and anger protocol; breathing exercises
  • Somatic complaints, sleep disturbance, and closing

There will be one facilitator and one co-facilitator. Groups will consist of 12-13 participants.

Primary outcomes

  1. Change in Kessler Psychological Distress Scale (K-10) over time

    Time frame: Change from baseline assessment (one week before the first session of CA-CBT) to follow-up assessment (1 month after post-assessment)

    K-10 is a 10-item scale that measures psychological distress. Each item is scored from 1 (none of the time) to 5 (all of the time) and ranges between 10 and 50. Higher scores indicate higher levels of psychological distress.

Secondary outcomes

  1. Change in Patient Health Questionnaire-9 (PHQ-9) over time

    Time frame: Change from baseline assessment (one week before the first session of CA-CBT) to follow-up assessment (1 month after post-assessment)

    PHQ-9 is a 9-item questionnaire that measures depressive symptoms. Each item is scored from 0 (not at all) to 3 (nearly every day) providing a range between 0 and 27. Higher scores indicate higher depressive symptoms.

  2. Change in Generalized Anxiety Disorder-7 (GAD-7) over time

    Time frame: Change from baseline assessment (one week before the first session of CA-CBT) to follow-up assessment (1 month after post-assessment)

    GAD-7 is a 7-item scale of general anxiety disorder that assesses anxiety symptoms. Each item is scored from 0 (not at all) to 3 (nearly every day) providing a range between 0 and 21. Higher scores indicate higher levels of anxiety.

  3. Change in World Health Organization Disability Assessment Schedule (WHODAS 2.0) over time

    Time frame: Change from baseline assessment (one week before the first session of CA-CBT) to follow-up assessment (1 month after post-assessment)

    WHODAS 2.0 is a 12-item scale that measures ability to engage in daily activities. Each item is scored from 1 (none) to 5 (extreme) and ranges between 12 and 60. Higher scores indicate higher levels of daily dysfunctioning.

  4. Change in Posttraumatic Stress Disorder (PTSD) Checklist for Diagnostic and Statistical Manual-5 (DSM-5) (PCL-5) over time

    Time frame: Change from baseline assessment (one week before the first session of CA-CBT) to follow-up assessment (1 month after post-assessment)

    PCL-5 is a 20-item questionnaire that assesses PTSD symptoms. Each item is scored from 0 (not at all) to 4 (extremely) providing a range between 0 and 80. Higher scores indicate higher levels of PTSD symptoms.

  5. Change in Prolonged Grief Disorder-13 (PG-13) over time

    Time frame: Change from baseline assessment (one week before the first session of CA-CBT) to follow-up assessment (1 month after post-assessment)

    The PG-13 instrument contains 13 items: two items (items 3 and 13) on duration and impairment that are to be answered "yes" or "no", and 11 items assessing cognitive, behavioral and emotional symptoms, rated on a 5-point scale. Items 1, 2, 4 and 5 are rated on a frequency scale ranging from: "not at all" to "several times a day" (scoring 1-5), and items 6-12 are rated on an intensity scale ranging from "not at all" to "overwhelmingly" (scoring 1-5). These total scores, ranging from 11 to 55. Higher total scores on the PG-13 indicate more severe symptoms of prolonged grief.

  6. Change in World Health Organization Quality of Life (WHOQOL-BREF) over time

    Time frame: Change from baseline assessment (one week before the first session of CA-CBT) to follow-up assessment (1 month after post-assessment)

    WHOQOL-BREF is a 26-item scale that measures quality of life. Each item is scored from 1 (not at all) to 5 (completely) providing a range between 26 and 130. Higher scores indicate higher levels of quality of life.

  7. Change in Multidimensional Scale of Perceived Social Support (MSPSS) over time

    Time frame: Change from baseline assessment (one week before the first session of CA-CBT) to follow-up assessment (1 month after post-assessment)

    MSPSS is a 12-item scale that measures perceived social support. Each item is scored from 1 (very strongly disagree) to 7 (very strongly disagree) providing a range between 12 and 84. Higher scores indicate higher levels of perceived social support.

  8. Change in World Health Organization-Five Well-Being Index (WHO-5) (1998) over time

    Time frame: Change from baseline assessment (one week before the first session of CA-CBT) to follow-up assessment (1 month after post-assessment)

    WHO-5 (1998) is a 5-item scale that measures well-being. Each item is scored from 0 (at no time) to 5 (all of the time) providing a range between 0 and 25. Higher scores indicate higher levels of well-being.

  9. Change in Dispositional Hope Scale (DHS) over time

    Time frame: Change from baseline assessment (one week before the first session of CA-CBT) to follow-up assessment (1 month after post-assessment)

    DHS is a 12-item scale that measures dispositional hope. Each item is scored from 1 (definitely false) to 8 (definitely true) providing a range between 12 and 96. Higher scores indicate higher levels of dispositional hope.

  10. Change in The Emotion Regulation Questionnaire (ERQ) over time

    Time frame: Change from baseline assessment (one week before the first session of CA-CBT) to follow-up assessment (1 month after post-assessment)

    ERQ is a 10-item questionnaire that measures emotion regulation. Each item is scored from 1 (strongly disagree) to 7 (strongly agree) providing a range between 10 and 70. Higher scores indicate higher levels of emotion regulation.

  11. Change in Acceptance and Action Questionnaire - version 2 (AAQ-2) over time

    Time frame: Change from baseline assessment (one week before the first session of CA-CBT) to follow-up assessment (1 month after post-assessment)

    AAQ-2 is a 7-item questionnaire that measures of psychological inflexibility, experiential avoidance, and potential psychological distress. Each item is scored from 1 (never true) to 7 (always true) providing a range between 7 and 49. Higher scores indicate higher levels of psychological inflexibility, experiential avoidance, and more potential psychological distress.

Sponsors and collaborators

Lead sponsor

Koç University

Other

Registry information

Official study title

Culturally Adapted Cognitive Behavioral Therapy to Reduce Psychological Distress of Individuals Affected by the Earthquake: A Pilot Randomized Controlled Trial

Acronym: CARED-ACT

Important dates

Study start
2024
Primary completion
2024
Study completion
2025
First posted
Jan 5, 2024
Registry last updated
Sep 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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