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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00373698
Other study ID # IAC 06-073
Secondary ID
Status Completed
Phase Phase 3
First received September 6, 2006
Last updated April 6, 2015
Start date March 2008
Est. completion date April 2012

Study information

Verified date June 2014
Source VA Office of Research and Development
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The study is an evaluation of a systemic intervention to enhance the delivery of care according to practice guidelines for posttraumatic stress disorder (PTSD). The immediate objectives are to (1) implement three component model (3CM) in VA primary care clinics; and (2) evaluate the effects of 3CM on clinician behavior and patient outcomes. The long-term objectives are to generate information to support implementation research on the RESPECT model for treating PTSD in primary care and ultimately, the implementation of the model in VHA to provide care to veterans with PTSD.


Description:

3CM consists of (1) a prepared practice, (2) care management, and (3) enhanced mental health support. A prepared practice refers to education for primary care clinicians and office staff about practice guidelines and evidence-based care, the skills needed for use of assessment measures, and the use of communication forms and routines. The education plan consists of predisposing activities, including active teaching and learning, and enabling and reinforcing activities in order to help clinicians use newly acquired skills and to reinforce the continued use of these skills in practice. Care management is accomplished by telephone, usually by a centrally located care manager during acute phase treatment and follow up to answer patient questions, promote adherence to the clinician's management plan, and help patients overcome barriers to adherence. Enhanced mental health support is provided by a psychiatrist who supervises care managers by telephone, provides informal consultation to primary care clinicians, and helps to increase the quantity or quality of mental health referral resources.


Recruitment information / eligibility

Status Completed
Enrollment 195
Est. completion date April 2012
Est. primary completion date April 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Military Veterans in Primary Care Clinics who meet diagnostic criteria for PTSD in one of the 5 sites in Texas where this study is being conducted.

- Must have regular access to a telephone and speak English.

Exclusion Criteria:

- Cognitive impairment

- A history of psychosis or mania

- Prominent current suicidal ideation

- Current substance dependence

- Current engagement in mental health treatment

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Intervention

Behavioral:
Three Component Model of Collaborative Care
Patients randomized to 3CM will receive telephone care management along with usual care by VA clinicians.

Locations

Country Name City State
United States VA North Texas Health Care System Dallas VA Medical Center, Dallas, TX Dallas Texas
United States Central Texas Veterans Health Care System, Temple, TX Temple Texas
United States Central Texas Veterans Health Care System Waco VA Medical Center, Waco, TX Waco Texas
United States White River Junction VA Medical Center, White River Junction, VT White River Junction Vermont

Sponsors (1)

Lead Sponsor Collaborator
VA Office of Research and Development

Country where clinical trial is conducted

United States, 

References & Publications (1)

Schnurr PP, Friedman MJ, Oxman TE, Dietrich AJ, Smith MW, Shiner B, Forshay E, Gui J, Thurston V. RESPECT-PTSD: re-engineering systems for the primary care treatment of PTSD, a randomized controlled trial. J Gen Intern Med. 2013 Jan;28(1):32-40. doi: 10.1 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary PTSD Symptom Severity PTSD Symptom Severity was measured using the Postraumatic Diagnostic Scale (PDS) 3 and 6 months after initial assessment No
Secondary Depression Measure using the Hopkins Symptom Checklist-20 3 and 6 months after initial assessment No
Secondary SF-36 Mental Component 3 and 6 months after initial assessment No
Secondary SF-36 Physical Component 3 and 6 months after initial assessment No
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