At a glance
ClinicalIndex Comparison RecordN/ACompleted· 426 enrolled
Drug / intervention
heart rate variability biofeedback +2 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Identification of and At-Risk Interventions for Pre-deployment Psychophysiologic Predictors of Post-deployment Mental Health Outcomes
In Brief
A clinical study evaluating heart rate variability biofeedback, Cognitive bias modification training, and 1 other intervention for Post-traumatic Stress Disorder. Completed, enrolled 426 participants across 1 site.
Detailed Summary
The primary objectives of this proposal are to develop objective pre-deployment predictors of PTSD and test two pre-deployment resiliency interventions.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPost-traumatic Stress Disorder
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
Enrollment StartSep 2008
First PostedFeb 2009
Primary CompletionSep 2013
TodayJul 2026
First PostedFeb 6, 2009
Enrollment StartSep 1, 2008
Primary CompletionSep 1, 2013
TodayJul 2, 2026
Enrollment to primary: 5 yearsPosted 17.4 years ago
Interventions
heart rate variability biofeedbackdevice
Heart rate variability biofeedback, 3 session plus handheld device
Cognitive bias modification trainingdevice
Cognitive bias modification training - 3 session plus handheld device
Sham Comparatordevice
Subjects received iPod without a study app and no additional resilience training