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Noninvasive Brain Stimulation
Active transcranial magnetic stimulation for Post-Traumatic Stress Disorder
N/A
Waitlist Available
Research Sponsored by Laval University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
18-60 years old
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 months
Awards & highlights
Study Summary
The purpose of this trial is to study the effect of noninvasive brain stimulation in adults with post-traumatic stress disorder.
Eligible Conditions
- Post-Traumatic Stress Disorder
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Severity of symptoms on the following clinical scale: PTSD symptoms as assessed by the Modified PTSD Symptom Scale (MPSS-SR)
Secondary outcome measures
Anxiety
Mental Depression
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: Active transcranial magnetic stimulationActive Control1 Intervention
Active transcranial magnetic stimulation will induce real pulses using the transcranial magnetic stimulation device.
Group II: Sham transcranial magnetic stimulationPlacebo Group1 Intervention
Sham transcranial magnetic stimulation will not induce any pulses using the same transcranial magnetic stimulation device but by also adding a sham block device.
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Who is running the clinical trial?
Laval UniversityLead Sponsor
417 Previous Clinical Trials
172,244 Total Patients Enrolled
Frequently Asked Questions
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