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Increasing Engagement in PTSD Treatment Through Patient Education and Patient Choice

NCT01446146 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 27

Last updated 2013-07-24

No results posted yet for this study

Summary

The purpose of this program is to compare two different methods of matching a Veteran to a PTSD treatment.

Conditions

  • Posttraumatic Stress Disorder (PTSD)

Interventions

BEHAVIORAL

Informed decision making

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.

BEHAVIORAL

Placebo session

Participant will complete clinician-administered measures in a 40-minute session.

Sponsors & Collaborators

  • South Central VA Mental Illness Research, Education & Clinical Center

    collaborator FED

  • Michael E. DeBakey VA Medical Center

    lead FED

Principal Investigators

  • Juliette M Mott, PhD · MDVAMC, BCM, SC MIRECC

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-10-31
Primary Completion
2013-01-31
Completion
2013-01-31

Countries

  • United States

Study Locations

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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 NCT01446146 on ClinicalTrials.gov