Post-traumatic Stress Disorder Clinical Trial
Official title:
The Use of Noninvasive Brain Stimulation in Post-traumatic Stress Disorder
The purpose of this trial is to study the effect of noninvasive brain stimulation in adults with post-traumatic stress disorder.
| Status | Recruiting |
| Enrollment | 28 |
| Est. completion date | March 2016 |
| Est. primary completion date | March 2016 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Both |
| Age group | 18 Years to 60 Years |
| Eligibility |
Inclusion Criteria: - 18-60 years old Exclusion Criteria: - Transcranial magnetic stimulation ineligibility |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Basic Science
| Country | Name | City | State |
|---|---|---|---|
| Canada | IRDPQ | Quebec |
| Lead Sponsor | Collaborator |
|---|---|
| Laval University |
Canada,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Severity of symptoms on the following clinical scale: PTSD symptoms as assessed by the Modified PTSD Symptom Scale (MPSS-SR) | Units will be the differences (%) in scores before and after the intervention | 2 months | Yes |
| Secondary | Severity of symptoms on the following clinical scale: anxiety symptoms as assessed by the Beck Anxiety Inventory (BAI) | Units will be the differences (%) in scores before and after the intervention | 2 months | Yes |
| Secondary | Severity of symptoms on the following clinical scale: depression symptoms as assessed by the Beck Depression Inventory (BDI) | Units will be the differences (%) in scores before and after the intervention | 2 months | Yes |
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