- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07010861
- Original Trial
Effects of Expressive Art Therapy Applied to Earthquake Victims Who Have Experienced Loss
May 30, 2025 updated by: Merve Kızılırmak Tatu
Effects of Expressive Art Therapy Applied to Earthquake Victims Who Have Experienced Loss on Psychological Symptoms and Post-Traumatic Growth: A Randomized Controlled Study
Earthquakes can negatively affect individuals' mental health by creating serious traumatic effects on individual and societal levels.
Traumatic experiences such as losing one's home or workplace, being injured, or losing a loved one cause individuals to develop long-term psychological symptoms.
In this context, strengthening psychosocial support programs aimed at coping with psychological and social problems after an earthquake is of great importance.
In this study, the effect of expressive art therapy applied to individuals who experienced losses due to the earthquakes centered in Kahramanmaraş on psychological symptoms and post-traumatic growth was examined.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
A randomized controlled intervention design with pre-test-post-follow-up measurements was used, which is one of the quantitative research methods.
In line with the power analysis, a total of 42 participants, 21 in each group, constituted the research sample.
The distribution of participants to the intervention and control groups was made with stratified block randomization.
The inclusion criteria of the study included being 18 years of age or older, knowing Turkish, and having experienced material and moral loss due to the earthquake; while the exclusion criteria were mental illness or receiving active psychosocial support.
The Brief Symptom Inventory (BSI) and the Post-Traumatic Growth Scale (PTS) were used as data collection tools.
The intervention process includes a six-session expressive arts therapy program.
The scales will be administered online at pre-test, post-test and two-month follow-up.
Data will be evaluated with repeated measures and two-way variance analyses.
It is expected that this study will contribute to post-traumatic recovery processes and art-based psychosocial interventions.
Study Type
Interventional
Enrollment (Actual)
42
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Çankaya
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Ankara, Çankaya, Turkey, 06500
- Gazi University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Being 18 years of age or older,
- Being able to understand, speak and write Turkish,
- Having directly experienced the earthquakes centered in Kahramanmaraş, -
- Having experienced material and moral losses due to the earthquakes centered in Kahramanmaraş
Exclusion Criteria:
- Having a neurological disorder that prevents communication,
- Actively receiving any psychosocial support/counseling
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
After the pre-test, the intervention program was started for the intervention group.
The expressive arts therapy program was applied in six sessions, each session lasting 60-90 minutes.
All sessions were conducted online.
Each session started with greetings and mood control, then a brief evaluation of the previous week was made.
The sessions consisted of three stages: giving instructions by the researcher, participants performing artistic actions with appropriate art elements and techniques, and participants working on sharing their artistic stimulation and associations.
A list of materials to be used in the session (pencils, paint, paper, play dough, etc.) was sent to the participants one week before the sessions and they were asked to provide them until the session.
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As a strategy for coping with trauma, art production creates therapeutic effects on the individual with its sensory and physical aspects (Chapman, 2013; King-West and Hass-Cohen, 2008).
When verbal expression is insufficient or carries the risk of re-traumatization, expressive art therapy offers a safe space through non-verbal expression (Talwar, 2007).
It is stated that art production is effective in repairing self-integrity ruptures that occur in traumatic experiences (Harris, 2009).
Through creative processes, the individual can restructure both internally and externally.
Expressive art therapy, especially when applied in a group environment, creates a psychotherapeutic effect by providing participants with the opportunity to express their emotions, imagination and unconscious processes (Malchiodi, 2012; Kim et al., 2021).
The commitment and reflective understanding that occur in group psychotherapy are among the factors that give hope and strength (Robb, 2017).
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No Intervention: Control
No intervention was made to the control group.
After the follow-up test was applied to the participants in the experimental group, a three-session expressive arts therapy program was applied to the control group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Brief Symptom Inventory (BSI)
Time Frame: Change from baseline to 6 weeks (also assessed at 14 weeks post-baseline)
|
It is a 53-item symptom screening scale developed by Derogatis.
The scale consists of 9 subscales and 3 global indexes.
The 9 subscales of the scale are, respectively, Somatization (S) (items 2, 7, 23, 29, 30, 33, 37), Obsessive-compulsive disorder (OCD) (items 5, 15, 26, 27, 32, 36), Interpersonal sensitivity (IS) (items 20, 21, 22, 42), Depression (D) (items 9, 16, 17, 18, 35, 50), Anxiety disorder (AD) (items 1, 12, 19, 38, 45, 49), Hostility (H) (items 6, 13, 40, 41, 46), Phobic anxiety (PA) (items 8, 28, 31, 43, 47), Paranoid ideation (PD) (items 4, 10, 24, 48, 51) and Psychoticism (P) (items 3, 14, 34, 44, 53).
Additional items (EM) (items 11, 25, 39, 52) include items related to eating and drinking disorders, sleep disorders, death and thoughts about death, and feelings of guilt.
The global indices are the Disorder Severity Index, the Symptom Total Index, and the Symptom Disorder Index, respectively.
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Change from baseline to 6 weeks (also assessed at 14 weeks post-baseline)
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Post-Traumatic Growth Scale (PTGS)
Time Frame: Change from baseline to 6 weeks (also assessed at 14 weeks post-baseline)
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The Posttraumatic Growth Inventory was developed by Tedeschi and Calhoun (1996) to measure the development that occurs in individuals after trauma.
The scale consists of 21 items and the items are scored on a 6-point scale from 0 to 5. The scores obtained from the scale vary between 0 and 105, and a high score indicates that the person has experienced a positive change, that is, growth, after the trauma.
Factor analysis determined that the scale has 5 sub-dimensions (positive change in interpersonal relationships, awareness of new opportunities, understanding the value of life, increasing personal resilience, and strengthening spirituality).
The internal consistency coefficient of the scale was reported as .93
(Kağan et al., 2012).
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Change from baseline to 6 weeks (also assessed at 14 weeks post-baseline)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 15, 2024
Primary Completion (Actual)
January 15, 2025
Study Completion (Estimated)
June 15, 2025
Study Registration Dates
First Submitted
May 30, 2025
First Submitted That Met QC Criteria
May 30, 2025
First Posted (Actual)
June 8, 2025
Study Record Updates
Last Update Posted (Actual)
June 8, 2025
Last Update Submitted That Met QC Criteria
May 30, 2025
Last Verified
May 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- 05.20.2024-E.950905
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Other researchers wiil be able to read detailed information such as the research method and results when the research is published.
The "Research Protocol" will be available on this PRS page.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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