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
Sponsors and collaborators
Womack Army Medical Center
Lead sponsor
Walter Reed National Military Medical Center
Collaborator
United States Department of Defense
Collaborator