Pathophysiological Understanding and Treatment of PTSD: an rTMS Approach

NCT03840369 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2022-11-04

No results posted yet for this study

Summary

In Canada, the prevalence of PTSD is approximately 12%, similar to Canadian military personnel. Current treatments for PTSD are limited in efficacy and durability - indicating a dire need for novel interventions in this population. Transcranial magnetic stimulation (TMS) has a high degree of safety and has been studied as an intervention for many mental health and neurological conditions; even showing initial promise for PTSD. We propose to study this further in a randomized sham controlled trial of TMS for PTSD.

Conditions

  • Stress Disorders, Post-Traumatic
  • Brain Injuries
  • Transcranial Magnetic Stimulation
  • Magnetic Resonance Spectroscopy
  • Biomarkers
  • Depression, Anxiety

Interventions

DEVICE

Repetitive Transcranial Magnetic Stimulation to Right Dorsolateral Prefrontal Cortex

Transcranial magnetic stimulation (TMS) works by delivering a magnetic pulse to a focal brain region. TMS has a high degree of safety and has been studied as an intervention for many mental health and neurological conditions. Repetitive TMS (rTMS) delivers pulses at a set time interval in order to modulate neural activity in that region.

DEVICE

Sham Repetitive Transcranial Magnetic Stimulation

The sham TMS coil will make a similar sound to the real rTMS coil, but will not deliver a magnetic pulse. This is a no-treatment device.

DEVICE

Repetitive Transcranial Magnetic Stimulation to Right Dorsomedial Prefrontal Cortex

Transcranial magnetic stimulation (TMS) works by delivering a magnetic pulse to a focal brain region. TMS has a high degree of safety and has been studied as an intervention for many mental health and neurological conditions. Repetitive TMS (rTMS) delivers pulses at a set time interval in order to modulate neural activity in that region.

Sponsors & Collaborators

  • Defence Research and Development Canada

    collaborator INDUSTRY
  • University of Calgary

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-06-01
Primary Completion
2022-02-18
Completion
2022-03-18

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03840369 on ClinicalTrials.gov