Support Groups in the Metaverse for Ukrainian Refugees — METASUPUKR  

Mental Health Wellness 1 Clinical Trial

Official title: Support Groups in the Metaverse for Ukrainian Refugees: A Randomized Clinical Trial

Status Recruiting

Clinical Trial Summary

The goal of this clinical trial is to test the efficacy of support groups held in the Metaverse, designed to promote mental health and well-being in Ukrainian refugees.

Participants:

• will be allocated to one of three conditions: (1) Metaverse support group (intervention); (2) In-Person support group (intervention); or (3) Waitlist.

• will be asked to participate in 5 support group sessions, once per week, for each intervention condition.

The Metaverse support groups will be compared with the In-Person support groups and with the Waitlist, to test:

• the efficacy of the Metaverse condition compared to the In-Person condition.

• the efficacy of the intervention conditions compared to the waitlist.

Clinical Trial Description

This protocol outlines a randomized clinical trial to assess the efficacy of virtual support groups (i.e., groups meeting in the Metaverse) for Ukrainian refugees. The study will provide essential insights into the potential benefits of using the Metaverse in delivering support group sessions. The results will contribute to the development of targeted and scalable interventions and policies to promote the well-being of Ukrainian refugees.

Participants will be recruited from Ukrainian refugee communities. The participants will be randomly assigned to one of three conditions: (1) Metaverse intervention group; (2) In-person intervention group; and (3) Waitlist. Stratification will consider factors such as age, gender, trauma history, and language proficiency to achieve balanced group distributions.

The In-Person and Metaverse groups will participate in five weekly support group sessions led by licensed psychologists.

All three groups will be evaluated at (1) pre-intervention (baseline), (2) after session no. 2, (3) post-intervention, and (4) 3-month follow-up.

G*Power analysis yields a total of N=45 (f = 0.25, power = 0.95) for the three conditions.

Statistical analysis plan: includes the analysis of primary and secondary outcomes, which will be assessed using predefined measures described at the measures section. Additionally, we will assess various predictors to gain insights into the factors influencing intervention outcomes. These predictors will be measured using specific instruments, including a screener (DSM-5-TR Self-Rated Level 1 Cross-Cutting Symptom Measure-adult version) and Working Alliance Inventory-Short Form (WAI-S). ;

Related Conditions & MeSH terms

• Mental Health Wellness 1

• NCT number: NCT06142032
• Study type: Interventional
• Source: University of Bucharest
• Contact: Cezar Giosan, PhD
• Phone: +40730908050
• Email: giosan@outlook.com
• Status: Recruiting
• Phase: N/A
• Start date: December 20, 2023
• Completion date: August 2024