CompletedNot Applicable

The Effect of Psychodrama and Virtual Reality-Supported Psychoeducation on Emotion Recognition Skills in Earthquake Survivors

Turkey (Türkiye)32 participantsStarted 2024-02-01

Plain-language summary

This study examined the effects of psychodrama and cognitive behavioral therapy (CBT)-based virtual reality (VR)-supported psychoeducation on facial emotion recognition skills in earthquake survivors using an artificial intelligence-based Facial Emotion Recognition System. It was conducted using a pre-test-post-test randomized quasi-experimental design. The sample consisted of 32 adult earthquake survivors affected by the February 6, 2023, Kahramanmaraş-centered earthquakes who were residing at the Temporary Accommodation Center. Participants were randomly assigned to two groups: a psychodrama group (n=16) and a VR-supported psychoeducation group (n=16). The first experimental group received 13 psychodrama sessions, held once a week, while the second group received CBT-based psychoeducation consisting of 10 sessions held once a week, with VR content incorporated at the end of each session. A Personal Information Form, a Semi-Structured Interview Form, and the Facial Emotion Recognition System were used as data collection tools. Findings based on the Facial Emotion Recognition System revealed that VR-supported psychoeducation produced more pronounced changes in immediate emotional responses, increasing levels of happiness and neutral affect while reducing expressions of fear, sadness, and anger. In conclusion, the results from the Facial Emotion Recognition System indicate that VR-supported psychoeducation had significant positive effects on participants' immediate emotional responses, reducing negative emotions while increasing happiness and neutral affect. In contrast, the psychodrama intervention did not produce a significant change in the measured immediate emotional responses. These findings can contribute to the planning and development of post-disaster mental health services.

Who can participate

Age range

18 Years – 60 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * The study included individuals aged 25 to 60 who possessed computeror technology skills, * were open to communication and collaboration, * had not previously participated in psychoeducation or psychodrama training, and whose homes sustained severe or moderate damage. Exclusion Criteria: * Individuals who were uncommunicative, had a psychiatric diagnosis according to hospital records, * had vision or hearing problems, had epilepsy, * had cancer, or were illiterate were excluded from the study.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

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Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Emotion Recognition Scores for the Psychoeducation and Psychodrama Groups

Timeframe: 5 months

Trial details

NCT IDNCT07754643

SponsorInonu University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-06-30

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