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

NCT01401101 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 404

Last updated 2016-09-02

Study results available
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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.

Conditions

  • Stress Disorders, Post-Traumatic

Interventions

OTHER

PCM

Care Manager (CM) intervention

OTHER

MEU

The MEU condition consists of only the clinician education and patient screening without written feedback.

Sponsors & Collaborators

  • Clinical Directors Network

    collaborator NETWORK

  • Georgetown University

    collaborator OTHER

  • University of Washington

    collaborator OTHER

  • RAND

    lead OTHER

Principal Investigators

  • Lisa S Meredith, PhD · RAND

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-06-30
Primary Completion
2014-02-28
Completion
2015-03-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01401101 on ClinicalTrials.gov