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N/A Completed N=359

Pain, Psychiatric Disorders, and Disability Among Veterans With and Without Polytrauma

Source: ClinicalTrials.gov NCT00645970 ↗
Enrolled (actual)
359
Serious AEs
0.0%
Results posted
Dec 2014
Primary outcomePrimary: Numeric Rating Scales of Pain Over Past Week (11 Point Likert Scale) — 4.66; 3.80; 4.92; 3.30 units on a scale

Summary

We believe information to be obtained from this proposed study will prove critical for planning future VA healthcare strategies and developing effective and efficient treatments targeting pain and emotional adjustment difficulties among individuals with polytrauma and returning Operation Enduring Freedom (OEF) and Operation Iraqi Freedom (OIF) personnel. More specifically, this study will be the first to provide systematic data regarding pain and emotional problem prevalence, course, associated impairments, risk factors, and barriers to care and community reintegration among returning OEF and OIF service members with and without polytrauma.

Outcome Measures

OutcomeResultp-value
PRIMARY
Numeric Rating Scales of Pain Over Past Week (11 Point Likert Scale)
4.66; 3.80; 4.92; 3.30; 4.88; 4.69

Eligibility Criteria

Inclusion Criteria

for Polytrauma Participants

  • Was deployed to Iraq or Afghanistan between October 2001 and the present
  • Meets the VA definition of polytrauma injury
  • Received medical clearance from attending physician to participate in study
  • Able to provide valid self-report of pain level using 0-10 numeric rating scale
  • Fluent in verbal and written English
  • Rancho Los Amigos level 6
  • Competent to provide full informed consent

for Non-Polytrauma Participants

  • Was deployed to Iraq or Afghanistan between October 2001 and the present
  • Fluent in verbal and written English
  • Able to provide valid self-report of pain level using 0-10 numeric rating scale
  • Competent to provide full informed consent

Exclusion Criteria

see above.

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00645970). 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. Informational only — not medical advice.

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