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Recruiting NCT06940986

NCT06940986 The PROmoting Pain Self-Management (PROs) Trial: Holistic Pain Care in the Military Health System

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Clinical Trial Summary
NCT ID NCT06940986
Status Recruiting
Phase
Sponsor Brooke Army Medical Center
Condition Chronic Pain
Study Type INTERVENTIONAL
Enrollment 608 participants
Start Date 2025-12-19
Primary Completion 2027-07-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Empowered ReliefMove to HealthUsual Care as determined by primary care provider

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 608 participants in total. It began in 2025-12-19 with a primary completion date of 2027-07-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this study is to improve pain care in the MHS by identifying effective, whole-person, non-pharmacologic interventions for persons with chronic musculoskeletal pain. The investigators will evaluate two promising, evidence-based holistic health interventions and compare them to usual care.

Eligibility Criteria

Inclusion Criteria: * Age 18 or older * TRICARE Beneficiary * Meets the case definition of chronic MSK pain requiring 2 or more medical encounters within the past year and at least 90 days apart for the same MSK condition indicated by medical encounter data or MSK pain ICD-10 codes in the electronic medical record Exclusion Criteria: * Actively receiving cancer treatment * Currently known to be pregnant * Receiving advanced chronic pain management, including multi-disciplinary or behavioral pain management or mental health or substance use programs (beyond the initial step of the VA/DoD stepped care model for pain management) * Suicidal Ideation determined by a higher than lower risk score on the P4 Screener * Currently undergoing post-surgical rehabilitation

Contact & Investigator

Central Contact

Tina Greenlee, PhD

✉ tina.a.greenlee.ctr@health.mil

📞 210-808-2575

Principal Investigator

Julie M Fritz, PhD

PRINCIPAL INVESTIGATOR

University of Utah

Frequently Asked Questions

Who can join the NCT06940986 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Chronic Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06940986 currently recruiting?

Yes, NCT06940986 is actively recruiting participants. Contact the research team at tina.a.greenlee.ctr@health.mil for enrollment information.

Where is the NCT06940986 trial being conducted?

This trial is being conducted at Fairbanks, United States, Schofield Barracks, United States, San Antonio, United States, San Antonio, United States and 1 additional location.

Who is sponsoring the NCT06940986 clinical trial?

NCT06940986 is sponsored by Brooke Army Medical Center. The principal investigator is Julie M Fritz, PhD at University of Utah. The trial plans to enroll 608 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology