Posttraumatic stress disorder intervention for people with severe mental illness in a low-income country primary care setting: a randomized feasibility trial protocol.

Journal: Pilot and feasibility studies

Volume: 7

Issue: 1

Year of Publication: 

Affiliated Institutions:  Department of Psychology, University of California Los Angeles, Los Angeles, CA, USA. Laurenng@ucla.edu. Department of Psychiatry, School of Medicine, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia. Centre for Innovative Drug Development and Therapeutic Trials for Africa (CDT-Africa), School of Medicine, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.

Abstract summary 

In this protocol, we outline a mixed-methods randomized feasibility trial of Brief Relaxation, Education and Trauma Healing (BREATHE) Ethiopia. BREATHE Ethiopia is a culturally and contextually adapted intervention for PTSD in participants with severe mental illness. BREATHE Ethiopia maps onto the World Health Organization's guidelines for posttraumatic stress disorder (PTSD) treatment in low- and middle-income country primary care settings.Specifically, this study includes a non-randomized pre-pilot (n = 5) and a randomized feasibility trial comparing BREATHE Ethiopia to Treatment as Usual (n = 40) to assess trial procedures, acceptability, and feasibility of intervention delivery, and investigate potential effectiveness and implementation. In a process evaluation, we will collect data that will be critical for a future fully randomized controlled trial, including the numbers of participants who are eligible, who consent, who engage in treatment, and who complete the assessments, as well as the feasibility and acceptability of assessments and the intervention. Qualitative data on facilitators and barriers to intervention delivery and quantitative data on provider fidelity to the intervention and participant and provider satisfaction will also be collected. Quantitative assessments at baseline, post-treatment, 1-month follow-up, and 3-month follow-up will assess change in mental health symptoms and functional impairment and hypothesized intervention mechanisms, including knowledge about PTSD, stigma, trauma-related cognitions, and physiological arousal.Findings from this study will inform a future fully-powered randomized controlled trial, and if found to be effective, the intervention has the potential to be integrated into mental healthcare scale-up efforts in other low-resource settings.Registered with ClinicalTrials.gov (NCT04385498) first posted May 13, 2020; https://www.clinicaltrials.gov/ct2/show/NCT04385498?term=ethiopia&cond=PTSD&draw=2&rank=1 .

Authors & Co-authors:  Ng Lauren C LC Serba Eyerusalem Getachew EG Dubale Benyam W BW Fekadu Abebaw A Hanlon Charlotte C

Study Outcome 

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Statistics
Citations :  World Health Organization . mhGAP Intervention Guide for mental, neurological and substance use disorders in non-specialized health settings. Geneva: World Health Organization; 2010. p. 107.
Authors :  5
Identifiers
Doi : 149
SSN : 2055-5784
Study Population
Male,Female
Mesh Terms
Other Terms
Global mental health;Intervention;PTSD;Primary care;Psychosis;Task-sharing
Study Design
Randomized Control Trial,Cross Sectional Study
Study Approach
Quantitative,Qualitative
Country of Study
Ethiopia
Publication Country
England