Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| South Central VA Mental Illness Research, Education & Clinical Center | FED |
The purpose of this program is to compare two different methods of matching a Veteran to a PTSD treatment.
Posttraumatic Stress Disorder (PTSD) is a serious disorder that affects many Veterans who have had a traumatic experience. The VA offers several different types of treatment for PTSD. We are researching different ways to match a Veteran to a type of treatment. Participants in this study will will be randomly assigned to either a 40-minute session in which they will learn about PTSD treatments and select a preferred treatment or to a 40-minute assessment interview. Those participants assigned to the assessment interview will have the opportunity to work with their Trauma Recovery Program provider to determine a plan for their PTSD treatment.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| IDM intervention | Experimental | Will receive a 40 minute intervention session with a clinician, learning about PTSD treatment options and choosing a preferred treatment. |
|
| Treatment as usual plus placebo session | Placebo Comparator | Will work with provider to select a treatment plan and will receive a 40 minute session without IDM intervention. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Informed decision making | Behavioral | 40 minute session with a clinician. Participants will learn about the available PTSD treatment options and will be given a decision aid with more information. |
| Measure | Description | Time Frame |
|---|---|---|
| Treatment participation | Trauma Recovery Program service utilization as assessed by chart review. | 4 months |
| Measure | Description | Time Frame |
|---|---|---|
| Treatment satisfaction | Assessed via self-report measures (Client Satisfaction Questionnaire, Credibility/Expectancy Questionnaire) and semi-structured interview | 4 months |
| Change in PTSD severity |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Juliette M Mott, PhD | MDVAMC, BCM, SC MIRECC | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Michael E. DeBakey VA Medical Center | Houston | Texas | 77030 | United States |
Not provided
| ID | Term |
|---|---|
| D013313 | Stress Disorders, Post-Traumatic |
| ID | Term |
|---|---|
| D040921 | Stress Disorders, Traumatic |
| D000068099 | Trauma and Stressor Related Disorders |
| D001523 | Mental Disorders |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Placebo session | Behavioral | Participant will complete clinician-administered measures in a 40-minute session. |
|
Assessed by the PCL-M at baseline and 4 month follow-up
| Baseline and 4 months |