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N/A N=345

Project SERVE: Post Deployment Functioning

Post-traumatic Stress Disorder · Depressive Disorder · Alcoholism

Enrolled (actual)
345
Serious AEs
9.1%
Results posted
Aug 2015
Primary outcome: Primary: World Health Organization Disability Assessment Schedule II (WHODAS II) — 1.87; 2.03; 2.07; 1.88 units on a scale

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
VA Office of Research and Development
Primary completion
Jun 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
World Health Organization Disability Assessment Schedule II (WHODAS II)
1.87; 2.03; 2.07; 1.88
SECONDARY
Inventory of Psychosocial Functioning (IPF)
2.51; 2.33
SECONDARY
Quality of Life Scale (QLS)
76.33; 73.04; 72.38; 77.59
SECONDARY
Clinician Administered PTSD Scale (CAPS-5)
29.71; 34.29

Summary

Functional recovery is of the utmost importance to evaluate in our returning Operation Enduring and Iraqi Freedom Veterans so that we can better understand their needs and experiences during the readjustment process from warzone to civilian life. Although most soldiers are resilient, concerning rates of PTSD (12-20%) and depression (14-15%) have been found, and as many as 24-35% report drinking more alcohol than they intended (Hoge et al., 2004). The current study proposes to follow returning Veterans for a one-year period to evaluate factors that influence the readjustment process and functional impairment. This information should guide the development of early intervention and treatment programs to help recovery.

Eligibility Criteria

Inclusion Criteria

To be eligible, participants must be:

  • enrolled returning OEF/OIF Veteran within CTVHCS;
  • English-speaking Veterans;
  • able to comprehend and sign the informed consent form;
  • able to complete the structured interviews and self-report assessments;
  • willing to be contacted for follow-up assessments;
  • deemed stable on psychotropic medications and in psychotherapy.

Exclusion Criteria

Veterans will be excluded if they:

  • plan to relocate out of the Central Texas area within four months of protocol initiation;
  • meet criteria for a diagnoses of schizophrenia, other psychotic disorders, or bipolar disorder;
  • report current hallucinations or delusions that are clearly not trauma-related; or
  • report current suicidal or homicidal risk warranting crisis intervention.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01123642). 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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