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Functional and Occupational Rehabilitation of Troops

An Effectiveness-Implementation Trial of Functional Restoration for Chronic Pain Management in Active Duty Military Personnel

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06898866
Acronym
FORT
Enrollment
480
Registered
2025-03-27
Start date
2026-06-01
Completion date
2028-01-01
Last updated
2026-01-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Musculoskeletal Pain

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.

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.

Interventions

None listed

Sponsors

The University of Texas Health Science Center at San Antonio
Lead SponsorOTHER
United States Department of Defense
CollaboratorFED
University of Washington
CollaboratorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

"patient referred to functional restoration program by provider"

Exclusion criteria

"patient not referred to functional restoration program by provider"

Design outcomes

Primary

MeasureTime frameDescription
Pain Impact Score (PIS)Baseline to 13 monthsThe Pain Impact Score (PIS) is based on the Defense and Veterans Pain Rating Scale (DVPRS), which measures 7-day average pain intensity (0-10 scale) and adaptive PROMIS pain interference and physical function using numeric, color, facial, and word descriptors and is validated. PROMIS T-scores are converted to compute the PIS, ranging from 8-50 with a higher score indicating greater pain.

Contacts

CONTACTAlan L Peterson, PhD
Petersona3@uthscsa.edu210.562.6700
CONTACTKatherine A Comtois, PhD, MPH
kcomtois@uw.edu206-744-1752

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026