MedPath

A Feasibility Trial of Eye Movement Desensitization and Reprocessing Therapy- Integrative Treatment Group Protocol for Ongoing Traumatic Stress In Road Traffic Accident Survivors for Reduction of Post-traumatic Stress Symptoms

Not Applicable
Recruiting
Conditions
Stress
Post Traumatic Stress Symptoms
Quality of Life (QOL)
Registration Number
NCT07027930
Lead Sponsor
University of the Punjab
Brief Summary

Road traffic accidents (RTAs) are a significant public health concern globally, accounting for a substantial proportion of morbidity and mortality. This study evaluates the feasibility and acceptability of the Eye Movement Desensitization and Reprocessing Integrative Group Treatment Protocol for Ongoing Traumatic Stress (EMDR-IGTP-OTS) in the reduction of posttraumatic stress symptoms, depression, and anxiety, while improving the quality of life in individuals who have experienced traffic accidents. Using a randomized control design, participants aged 18-45 will be assessed at three-time points: pre-treatment, post-treatment, and one-month follow-up. The study employs the DASS-21, UIES-R, and WHOQOL-BREF as evaluation measures. Findings aim to expand evidence on trauma-focused interventions and explore their applicability in culturally diverse, resource-constrained settings.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
35
Inclusion Criteria
  • Aged between 18 and 45 years.
  • Experienced a traffic accident 3 months to 10 years prior
  • Willing to participate and able to understand the intervention components.
Exclusion Criteria
  • Participants will be excluded from the study if they meet any of the following criteria:

    • Diagnosed with conditions such as schizophrenia or bipolar disorder, which require specialized treatment beyond the scope of this study.
    • History of severe head injuries resulting in neurological or cognitive deficits.
    • Participants who have experienced a traffic accident less than 3 months ago, as immediate post-traumatic responses may not have stabilized

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
The Urdu Impact of Event Scale-RevisedFrom Enrollment to end of study after 4 weeks

It will measure trauma-specific symptoms such as intrusion, avoidance, and hyperarousal. This 22-item scale uses a 5-point Likert scale ranging from 0 (not at all) to 4 (extreme), comprehensively evaluating the psychological impact of traumatic incidents. Higher the scores, Higher will be severity of post traumatic symptoms.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Public Universities

🇵🇰

Lahore, Punjab, Pakistan

Public Universities
🇵🇰Lahore, Punjab, Pakistan

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.