Phase 2
N=404
Violence and Stress Assessment (ViStA) Project to Improve Post Traumatic Stress Disorder Management in Primary Care
Stress Disorders, Post-Traumatic
Bottom Line
View on ClinicalTrials.gov: NCT01401101 ↗Enrolled (actual)
404
Serious AEs
0.0%
Results posted
Sep 2016
Primary outcome: Primary: PTSD Symptoms — 71.1; 71.0 CAPS scores — p=0.97
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- PCM (Other); MEU (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- RAND
- Primary completion
- Feb 2014
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY PTSD Symptoms |
46.9; 44.2 | 0.33 |
| PRIMARY PTSD Symptoms |
46.9; 44.2 | 0.33 |
| PRIMARY PTSD Symptoms |
46.9; 44.2 | 0.33 |
Summary
The purpose of this study is to conduct a randomized trial of a Post Traumatic Stress Disorder (PTSD) Care Management (PCM) program to detect, treat, and improve PTSD treatment processes and outcomes in patients seeking primary care from FQHCs and evaluate its effectiveness on improving the processes and outcomes of care for PTSD.
Eligibility Criteria
Inclusion Criteria
- Has PTSD
- Has a scheduled or walk-in appointment with a participating PCC
- Speaks English of Spanish
- Is between 18 and 65 years old
- Expects to receive care in the CHC during the next year
Exclusion Criteria
- Acutely ill and cannot participate in a discussion
- Does not understand the information
Data sourced from ClinicalTrials.gov (NCT01401101). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.