Thinking of joining a study?

Register your interest

NCT06898866 | NOT YET RECRUITING | Chronic Musculoskeletal Pain


Functional and Occupational Rehabilitation of Troops
Sponsor:

The University of Texas Health Science Center at San Antonio

Brief Summary:

The proposed implementation science project will evaluate the factors that support or hinder the successful implementation of the FORT Functional Restoration Program at six Military Treatment Facilities (MTF) across the Military Health System. It will also evaluate the associated effectiveness outcomes related to chronic musculoskeletal pain management in active-duty military personnel.

Condition or disease

Chronic Musculoskeletal Pain

Detailed Description:

This project will be an effectiveness-implementation hybrid type 2 study design using a stepped-wedge randomized clinical trial research design. The study will simultaneously evaluate clinical and implementation outcomes related to the establishment of functional restoration programs. The study investigators have collaborated with the Defense Health Agency (DHA) Pain Management Clinical Support Services to identify chronic pain management programs at six MTFs interested in systematically improving and assessing the outcomes of their program. The MTFs will be randomized in pairs to initiate the Implementation Facilitation strategy to improve the implementation of their program over three 6-month intervals, after an initial 6-month baseline. This hybrid design will allow for the evaluation of both implementation and clinical effectiveness research aims and support rapid translation of research outcomes. Each site will participate in a minimum 6-month baseline period prior to the intervention period to serve as its own treatment as usual.

Study Type : OBSERVATIONAL
Estimated Enrollment : 480 participants
Official Title : An Effectiveness-Implementation Trial of Functional Restoration for Chronic Pain Management in Active Duty Military Personnel
Actual Study Start Date : 2025-07
Estimated Primary Completion Date : 2028-01
Estimated Study Completion Date : 2028-01

Information not available for Arms and Intervention/treatment

Ages Eligible for Study:
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • "patient referred to functional restoration program by provider"
Exclusion Criteria
  • "patient not referred to functional restoration program by provider"

Functional and Occupational Rehabilitation of Troops

Location Details

NCT06898866


Please Choose a site



How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations


No Location Found

Loading...