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N/A N=838

Prospective Study of Veteran Health in Previously Deployed Soldiers

Combat Disorders

Enrolled (actual)
838
Serious AEs
0.0%
Results posted
Oct 2014
Primary outcome: Primary: Non-Specific Physical Symptoms — 5.2; 7.9; 7.7; 7.7 units on a scale

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Adult · 18+ yrs
Sex
All
Sponsor
US Department of Veterans Affairs
Primary completion
Feb 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Non-Specific Physical Symptoms
5.2; 7.9; 7.7; 7.7
PRIMARY
Physical Functional Status
55.5; 53.7; 52.8; 51.5
PRIMARY
Mental Functional Status
48.0; 45.7; 45.0; 44.9
PRIMARY
Health Care Utilization
0.78; 0.68; 0.69; 1.11

Summary

Background: Previous deployments like that to the Persian Gulf in 1991 produced veterans with post-deployment symptom-based health problems with no medical explanation. This was termed Gulf War illness or medically unexplained illness (MUI). If previous wars are any indication, some soldiers currently deployed to hostile areas also will return home with unexplained symptom-based illnesses. However, when this study began there was virtually no pre-war, prospective data on risk and resilience factors associated with MUI. This study is attempting to fill that gap. Objectives: Our goals are to: (a) determine pre- and immediate post-deployment factors predicting later MUI and poor functional status, (b) improve previous methodological problems (e.g., selection bias, recall bias and lack of baseline controls) in studies of MUI, and (c) relate pre-deployment risk factors (e.g., personality, stressor reactivity) and resilience factors (e.g., coping style, social support) to post-deployment functional status.

Eligibility Criteria

Inclusion Criteria

  • Army Reserve and National Guard soldiers deploying to a hazardous deployment from Fort Dix, New Jersey (NJ) and Camp Shelby, Mississippi (MS)

Exclusion Criteria

  • There are some drug exclusions for anything that substantially affects cardiovascular function.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00285246). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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