Status:

COMPLETED

Reduction of Risk for Low Back Injury in Theater of Operations

Lead Sponsor:

University of South Florida

Collaborating Sponsors:

Brooke Army Medical Center

Conditions:

Lower Back Injury

Eligibility:

All Genders

18-35 years

Phase:

NA

Brief Summary

The investigators will conduct a controlled clinical trial with U.S. Army soldiers training to become combat medics. The purpose of this study is to determine if a 11-week, high intensity exercise pro...

Detailed Description

Background Low back injury is responsible for the largest percentage of non-battle injuries in the theater of operations and is a large contributor to non-expiration of active service attrition in the...

Eligibility Criteria

Inclusion

  • Age 18-35 years
  • Active duty soldiers in the US Army training to become combat medics at Fort Sam Houston

Exclusion

  • Cardiovascular contraindications to resistance exercise as identified by history and physical examination
  • Orthopedic contraindications to resistance exercise as identified by history and physical examination
  • History of systemic inflammatory disease or spinal surgery
  • Low back pain intensity \> "mild"
  • Disability \>= 50% on the Roland Morris Disability Questionnaire
  • Currently receiving care for spinal pain disorder/injury
  • Currently disabled due to spinal pain disorder/injury
  • Currently diagnosed with or receiving treatment for a psychological or psychiatric disorder
  • Currently performing progressive resistance exercises for the lumbar extensor muscles other than those included in standard for military fitness programs
  • Active workers' compensation or personal injury case
  • Pregnant
  • Simultaneously enrolled in another biomedical clinical trial
  • Drug or alcohol abuse within the past year
  • Any other condition, which in the opinion of the investigators or military medical authority, would put the candidate at increased safety risk or otherwise make the candidate unsuitable for this study
  • Unable or unwilling to complete the study procedures

Key Trial Info

Start Date :

June 1 2012

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 1 2015

Estimated Enrollment :

582 Patients enrolled

Trial Details

Trial ID

NCT01401842

Start Date

June 1 2012

End Date

March 1 2015

Last Update

May 25 2015

Active Locations (2)

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Page 1 of 1 (2 locations)

1

University of South Florida

Tampa, Florida, United States, 33612

2

Brooke Army Medical Center

Fort Sam Houston, Texas, United States, 78234