Deep Brain Reorienting in Post-traumatic Stress Disorder

Status Recruiting

Clinical Trial Summary

This study will evaluate the efficacy of a therapeutic treatment, Deep Brain Reorienting (DBR), for PTSD (Post-traumatic Stress Disorder). Participants will be randomized to either the DBR treatment, or wait-list condition.

Clinical Trial Description

This study will evaluate the efficacy of Deep Brain Reorienting (DBR) in reducing PTSD symptoms. DBR was designed by Dr. Frank Corrigan, a Scottish psychiatrist interested in the brain mechanisms underlying effective trauma psychotherapy. For this study, participants will be randomized to either the DBR treatment or wait-list study conditions. Trauma processing through DBR involves bringing up a traumatic memory and encourages the client to focus on tensions arising in the muscles of the shoulders, neck, head and face (i.e., those involved in orienting toward a threatening person/event). It is believed that this approach will allow the participant to process the traumatic memory in an emotionally manageable way, changing how it is represented/accessed in the brain's innate defensive system. Online Stream - Assessments will include clinical interviews (pre/post treatment, and follow-up) using Webex video conferencing, and fMRI (functional magnetic resonance imaging) scans (pre/post treatment). In-Person Stream - Assessment will include clinical interviews (pre/post treatment and follow-up), and fMRI scans (pre/post treatment). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04317820
Study type	Interventional
Source	Lawson Health Research Institute
Contact	Suzy - Study Coordinator
Phone	519-685-8500
Email	Suzy.Southwell@lhsc.on.ca
Status	Recruiting
Phase	N/A
Start date	September 29, 2020
Completion date	September 2024

View Details

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