Sensory Motor Arousal Regulation Treatment (SMART) Study

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorLondon Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

About this trial

This study will investigate whether a movement and body-based treatment can benefit adults with Post-traumatic Stress Disorder (PTSD). The treatment is called Sensory Motor Arousal Regulation Treatment, or "SMART", and study participation involves 8 sessions of SMART, as well as pre-treatment, post-treatment, and 3-month follow-up assessments.

Eligibility criteria

Qualifiers

Adults, aged 18-65

A primary diagnosis of PTSD as determined by our pre-treatment assessment

Ability to provide informed consent

Fluency in written and spoken English (to be able to complete assessments)

Disqualifiers

any implants, conditions, etc. that do not comply with 7T (Tesla) fMRI research safety standards (e.g., pacemaker, pregnancy/possible pregnancy)

history of significant head injury/lengthy loss of consciousness (e.g., a Glasgow Coma Scale Score < 15 at the time of incident as assessed retrospectively by participant)

significant untreated medical illness

history of neurological or neurodevelopmental disorder

Trial design

Treatments tested in this trial

  • SMART

Treatment groups

80 Participants
are divided into 2 treatment groups