Post-Traumatic Stress Disorder (PTSD) Clinical Trials

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Mindfulness-based Stress Reduction for Treatment of PTSD in Road Traffic Accident Victims: Evaluating Its Efficacy in a Randomised Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goals of the study are to investigate the effects of mindfulness-based stress reduction (MBSR) on PTSD among road traffic accident victims. The main questions are: does MBSR exerts any effects on PTSD symptoms, quality of life and mindfulness? Researchers will compare effects of MBSR with TAU on PTSD symptoms, quality of life and mindfulness. Participants will be: * administered few questionnaires at three time points * administered MBSR once a week session for 6 weeks

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 60
Healthy Volunteers: f
View:

• (a) Possession of a road traffic identification certificate issued by the public security traffic police department; (b) Age 18-60 years; (c) junior high school education or above and full civil capacity; (d) those who meet the diagnostic criteria for PTSD according to DSM-5-TR (Diagnostic and Statistical Manual for Mental Disorder 5th Edition-Text Revised) which occurred after road traffic accident; (e) A score of 31 or above on the PTSD Checklist for DSM-5 (PCL-5) indicating possibility of PTSD in diagnosis; and (f) those taking a stable dose of a single antidepressant for the past 2 weeks and willing to maintain on the dose until the end of the study.

Locations
Other Locations
China
Fifth Affiliated Hospital of Xinjiang Medical University
RECRUITING
Ürümqi
Contact Information
Primary
Mohammad Farris Iman Leong Bin Abdullah, Doctor of Psychiatry
farrisiman@unisza.edu.my
+60186669950
Time Frame
Start Date: 2025-08-01
Estimated Completion Date: 2026-04-15
Participants
Target number of participants: 110
Treatments
Experimental: Mindfulness-based stress reduction group
The intervention in the MBSR group will be carried out as group therapy in a 2.5 hours (with 45 minutes home assignment) once a week session for 8 weeks. Home assignments will be provided at the end of each session. The acceptable number of sessions attended is at least six sessions, whereby those who attended less than that is considered to have insufficient intervention sessions.
No_intervention: Control Group
In the TAU control group, it will be carried out as group therapy in a 2.5 hours (with 45 minutes home assignment) once a week session for 8 weeks. Home assignments will be provided at the end of each session. Non-specific and non-therapeutic components will be explained to participants. The acceptable number of sessions attended is at least six sessions, whereby those who attended less than that is considered to have insufficient intervention sessions.
Related Therapeutic Areas
Sponsors
Leads: Universiti Sains Malaysia
Collaborators: Universiti Sultan Zainal Abidin, Xinjiang Medical University, Jinzhou Medical University

This content was sourced from clinicaltrials.gov