๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-05-29

Pre- and Post-neuromusculoskeletal Injury Risk Evaluation for Return-to-Duty Enhancement (NCT05111925)

Pre-neuromusculoskeletal Injury Risk Factor Evaluation and Post-neuromusculoskeletal Injury Assessment for Return-to-duty/Activity Enhancement

๐ŸŸข Recruiting Interventional Protocol ๐Ÿ“Š Observational Clinical Research Sponsor: Womack Army Medical Center

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

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.

Who can join: Review the eligibility criteria below.

Location: Walter Reed National Military Medical Center โ€” Bethesda, Maryland

Age range: 18 Years to 44 Years

๐Ÿงช Interventions in This Study

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

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (2 Sites)

  • Walter Reed National Military Medical Center โ€” Bethesda, Maryland
  • Womack Army Medical Center โ€” Fort Liberty, North Carolina

๐Ÿ“ž Contact the Study Coordinator

Phone: (910) 849-7226

Email: timothy.c.mauntel.civ@health.mil

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—