Violence and Stress Assessment (ViStA) Project to Improve Post Traumatic Stress Disorder Management in Primary Care



Status:Completed
Conditions:Psychiatric
Therapuetic Areas:Psychiatry / Psychology
Healthy:No
Age Range:18 - 65
Updated:5/5/2014
Start Date:June 2010
End Date:August 2013
Contact:Lisa S. Meredith, PhD
Email:seidel@rand.org
Phone:310-393-0411

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Improving PTSD Management in Primary Care

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 CHCs and evaluate its
effectiveness on improving the processes and outcomes of care for PTSD.

Post-traumatic Stress Disorder (PTSD) is a common problem seen in primary care but the
identification and management of PTSD is not routine and would benefit from new approaches.
Efforts must overcome patient-, clinician-, and system-level barriers, such as patients'
fear of stigma, clinician's time constraints for dealing with psychological issues, gaps in
clinician treatment knowledge, and difficulty arranging for referrals to mental health
specialists.

Unlike mood disorders such as depression, little is known about improving care for PTSD in
primary care settings. However, previous experience for treating depression, as well as
existing guidelines for addressing PTSD in primary care, provide evidence that effective
interventions exist and that multi-faceted interventions are more effective than a
single-component approaches.

In this project, the RAND Corporation, Clinical Directors Network Inc., Georgetown
University Department of Psychiatry, and University of Washington will implement and
evaluate a randomized controlled trial (RCT) of a PTSD Care Management (PCM) intervention to
detect, treat, and improve PTSD treatment processes and health outcomes in patients seeking
primary care from Community Health Centers (CHCs) in Northeastern USA.

The three specific aims are to:

1. Evaluate the effectiveness of the PCM intervention compared to a Treatment-as-Usual
(TAU) control in reducing PTSD and other mental health symptoms, and improving
patients' health-related quality-of-life.

2. Assess the success of the PCM intervention implementation and,

3. Examine the direct costs of the PCM intervention compared to the TAU control treatment.

The PCM intervention was developed using principles of Community-Based Participatory
Research (CPBR) methods in CHCs that provide care to the underserved, and is tailored to the
settings and populations we will study. This intervention is multi-faceted and includes
components and strategies implemented through a Care Manager (CM) to overcome patient-,
clinician-, and system-level barriers.

There are six PCM intervention components: 1) patient education, 2) patient screening and
written feedback of screening information to primary care clinicians, 3) clinician education
on practice guidelines , 4) structured feedback between primary care and mental health
clinicians, 5) continuity of patient care, and 6) a resource guide detailing available
community services where the CHC has established reciprocal referrals. All of the
intervention components will be implemented through the CM, except for the clinician
education component, which will combine onsite and online continuing medical education
(CME)-accredited sessions. The TAU condition will consist of only the clinician education
and patient screening without written feedback.

Patients will be interviewed during a pre-screening stage to determine PTSD status. A total
of 400 of the patients who screen positive will be randomly assigned to the PCM intervention
or TAU.

Data will be collected from several sources. First, patients will be assessed at baseline,
6 and 12 months via interviews using validated instruments. Second, CMs will compile
monthly aggregate data on patient management for patients assigned to the PCM program.
Third, CHC staff will be asked for their feedback about their experiences with implementing
the program at the end of the study. The study team will use these data to estimate the
direct costs of implementing the PCM program.

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
We found this trial at
7
sites
Bronx, New York 10473
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Far Rockaway, New York 11691
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Far Rockaway, NY
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Jersey City, New Jersey 07304
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Jersey City, NJ
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New York, New York 10009
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New York, NY
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Port Chester, New York 10573
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Port Chester, NY
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