Other Clinical Trial - Efficacy, Feasibility, & Acceptability of

Status Not yet recruiting

Clinical Trial Summary

The aim of this study is to develop a post-earthquake, trauma-focused Acceptance and Commitment Therapy (ACT)-based psychosocial intervention program (DeST-ACT) and to examine its effectiveness, feasibility, and acceptability of this program in enhancing life satisfaction and psychological flexibility in individuals exposed to earthquake trauma. In this regard, the main hypothesis is that the DeST-ACT psychosocial intervention program is effective, feasible, and acceptable among individuals exposed to earthquake trauma, including both primary and secondary outcomes of the program.

Clinical Trial Description

This quantitative, randomized controlled trial involves two groups and includes a pre-test and repeated post-tests. The study aims to assess the effectiveness, feasibility, and acceptability of the developed DeST-ACT program in addressing post-traumatic stress disorder, psychological flexibility, life satisfaction, values-based living, and depression-anxiety-stress levels in individuals affected by the February 6, 2023 earthquake. Participants will be randomly assigned to experimental and control groups in a 1:1 ratio using an internet-based block randomization program. The DeST-ACT psychosocial intervention program consists of a 4-session online intervention supported by self-help materials. Each session in the 4-week program is held once a week for 50 minutes. The main hypotheses are: - The intervention group will demonstrate a significant decrease in Post Traumatic Stress Disorder (PTSD) and depression-anxiety-stress levels compared to the control group. - The intervention group will experience a greater increase in values-based living, life satisfaction, and psychological flexibility over time compared to the control group. - The intervention group will demonstrate a significant decrease in PTSD and depression-anxiety-stress levels compared to baseline measures. - The intervention group will experience a greater increase in values-based living, life satisfaction, and psychological flexibility over time compared to baseline measures. ;

Study Design

Related Conditions & MeSH terms

Trauma and Stressor Related Disorders
Wounds and Injuries

Clinical Trial Details

NCT number	NCT06429852
Study type	Interventional
Source	CanSagligi Foundation
Contact	Aleyna Güleryüz, BA
Phone	02122696611
Email	aleyna-glrz@outlook.com
Status	Not yet recruiting
Phase	N/A
Start date	June 2024
Completion date	October 2024

View Details

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Efficacy, Feasibility, and Acceptability of the DeST-ACT: Trauma-Focused Acceptance and Commitment Therapy Program

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms