Actively Recruiting

Age: 18Years - 44Years
All Genders
Healthy Volunteers
NCT05111925

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

Led by Womack Army Medical Center · Updated on 2024-08-15

2690

Participants Needed

2

Research Sites

135 weeks

Total Duration

On this page

Sponsors

W

Womack Army Medical Center

Lead Sponsor

W

Walter Reed National Military Medical Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 44Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Active duty Service members cleared for full physical activity
  • Age between 18 and 44 years
  • For injured cohort: receiving conservative treatment for a musculoskeletal injury affecting the low back or lower extremity
  • Injured participants can be recruited at any time after presenting to rehabilitation care
  • For pilot cohort: active duty Service members cleared for full physical activity aged 18-44 years
Not Eligible

You will not qualify if you...

  • Currently on limited duty status for any reason (pilot and uninjured cohorts)
  • Unable to read or comprehend the English language
  • Pregnant females (eligible after pregnancy)
  • Scheduled for deployment or separation within the next 12 months (uninjured cohorts)
  • History of musculoskeletal injury within the last 6 months (injured cohorts)
  • History of lower extremity or low back musculoskeletal surgery (injured cohorts)
  • History of moderate or severe traumatic brain injury (injured cohorts)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Walter Reed National Military Medical Center

Bethesda, Maryland, United States, 20889

Actively Recruiting

2

Womack Army Medical Center

Fort Liberty, North Carolina, United States, 28310

Actively Recruiting

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Research Team

T

Timothy C Mauntel, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

5

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