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Psychophysiologic Predictors of Post-deployment Mental Health Outcomes

NCT00838006 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 426

Last updated 2020-07-02

Study results available
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Summary

The primary objectives of this proposal are to develop objective pre-deployment predictors of PTSD and test two pre-deployment resiliency interventions.

Conditions

  • Post-traumatic Stress Disorder

Interventions

DEVICE

heart rate variability biofeedback

Heart rate variability biofeedback, 3 session plus handheld device

DEVICE

Cognitive bias modification training

Cognitive bias modification training - 3 session plus handheld device

DEVICE

Sham Comparator

Subjects received iPod without a study app and no additional resilience training

Sponsors & Collaborators

  • Biomedical Research Foundation

    lead OTHER

Principal Investigators

  • Jeffrey M Pyne, MD · Central Arkansas Veterans Healthcare System

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2008-09-30
Primary Completion
2013-09-30
Completion
2013-09-30

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 NCT00838006 on ClinicalTrials.gov