Massed versus standard prolonged exposure for posttraumatic stress disorder in Australian military and veteran populations (RESTORE trial): Study protocol for a non-inferiority randomized controlled trial.


Journal

Contemporary clinical trials
ISSN: 1559-2030
Titre abrégé: Contemp Clin Trials
Pays: United States
ID NLM: 101242342

Informations de publication

Date de publication:
08 2021
Historique:
received: 03 02 2021
revised: 08 06 2021
accepted: 08 06 2021
pubmed: 14 6 2021
medline: 25 9 2021
entrez: 13 6 2021
Statut: ppublish

Résumé

Posttraumatic stress disorder (PTSD) can be a severe problem, affecting veterans and military personnel at higher rates than the general community. First-line treatment for PTSD, prolonged exposure (PE), is typically delivered weekly for 10-12 weeks, however this duration can pose a barrier to accessing and completing the treatment, particularly for current serving military. This paper presents the RESTORE trial protocol, the first randomized controlled trial of massed PE therapy outside of the United States and by an independent research group. One hundred and thirty-five Australian Defence Force members and veterans (18-80 years) who meet criteria for PTSD related to a military trauma will be randomly allocated to one of two conditions: standard PE (SPE; 10 weekly 90-min sessions) or massed PE (MPE; 10 daily 90-min sessions). Across eight sites, patients will be assessed at pre-treatment, and at 4 weeks, 12 weeks, and 12 months post-treatment commencement. The primary outcome is clinician-measured and self-reported PTSD symptom severity at the 12 week assessment. We hypothesize that MPE will be as effective as SPE in reducing PTSD severity at 12 weeks post-treatment commencement. The adaptation and testing of evidence-based interventions is critical to reduce barriers to treatment uptake among veterans and military personnel. Outcomes of this study have the potential to result in international, cross-service uptake and delivery of this rapid treatment for veterans and military members, as well as civilians, thereby improving clinical outcomes for patients and their families.

Identifiants

pubmed: 34119717
pii: S1551-7144(21)00214-7
doi: 10.1016/j.cct.2021.106478
pii:
doi:

Types de publication

Clinical Trial Protocol Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

106478

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Auteurs

Lisa Dell (L)

Phoenix Australia Centre for Posttraumatic Mental Health, Department of Psychiatry, The University of Melbourne, Carlton, VIC, Australia. Electronic address: lisa.dell@unimelb.edu.au.

Alyssa M Sbisa (AM)

Phoenix Australia Centre for Posttraumatic Mental Health, Department of Psychiatry, The University of Melbourne, Carlton, VIC, Australia.

Meaghan O'Donnell (M)

Phoenix Australia Centre for Posttraumatic Mental Health, Department of Psychiatry, The University of Melbourne, Carlton, VIC, Australia.

Peter W Tuerk (PW)

Sheila C. Jonson Centre for Clinical Services, Department of Human Services, University of Virginia, Charlottesville, VA, USA.

Richard Bryant (R)

School of Psychology, University of New South Wales, Sydney, NSW, Australia.

Stephanie Hodson (S)

Department of Veteran's Affairs, Canberra, ACT, Australia.

David Morton (D)

Department of Defence, Canberra, ACT, Australia.

Malcolm Battersby (M)

College of Medicine and Public Health, Flinders University, Bedford Park, SA, Australia.

Andrew Forbes (A)

School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.

David Forbes (D)

Phoenix Australia Centre for Posttraumatic Mental Health, Department of Psychiatry, The University of Melbourne, Carlton, VIC, Australia.

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Classifications MeSH