Pre- and Post-neuromusculoskeletal Injury Risk Evaluation for Return-to-Duty Enhancement

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-44
SponsorWomack Army Medical Center

About this trial

The purpose of this study is to develop comprehensive and efficient pre- and post- musculoskeletal injury (MSKI) risk assessments for Service members, incorporating both objective and subjective measures. This is a multi-site observational study to identify the pre- and post-MSKI physical and psychosocial factors contributing to MSKI risks and undesired patient outcomes following MSKI. The study hypothesis is that a set of field-expedient clinical assessments can identify Service member specific MSKI risk factors and post-MSKI deficits that contribute to undesired patient outcomes and provide data to guide patient-specific risk mitigation and rehabilitation programs.

Eligibility criteria

Qualifiers

Active duty Service members cleared for full physical activity.

18-44 years old

Active duty Service members cleared for full physical activity.

18-44 years old

Disqualifiers

Currently on limited duty status, for any reason.

Unable to read or comprehend the English language.

Pregnant females (will be eligible for participation in the study after the pregnancy)

Currently on limited duty status, for any reason.

Trial design

Treatments tested in this trial

  • PREPARE Initial Clinical Assessment - Pilot (two iterations)
  • PREPARE Initial Clinical Assessment - Pre-Injury (one iteration)
  • PREPARE Initial Clinical Assessment - Post-Injury (up to three iterations)
  • PREPARE Optimized Clinical Assessment

Treatment groups

2,690 Participants
are divided into 5 treatment groups

Sponsors and collaborators

Womack Army Medical Center

Lead sponsor

Walter Reed National Military Medical Center

Collaborator

United States Department of Defense

Collaborator