Mindfulness interventions for military patients after knee surgery
Official title: SMART Embedded Intervention for Military Postsurgical Engagement Readiness
Run by University of Utah · NCT05050409 · Data updated 2026-11-12
This study tests if mindfulness programs can help military patients recover better after knee surgery and reduce their need for pain medication.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | University of Utah Academic / other |
| Locations | 1 site (Fort Sam Houston, Texas) |
| Status | Recruiting |
| Started | May 1, 2022 |
| Main results expected | July 2027 |
| Study ends | October 2027 |
| Registry record updated | March 27, 2025 |
| Trial ID | NCT05050409 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are military personnel scheduled for unilateral total knee arthroplasty who are TRICARE beneficiaries.
✕Probably not a fit
Patients with cognitive impairments, recent contralateral knee surgeries, or current cancer diagnoses may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to optimize the use of mindfulness-based interventions for military patients undergoing total knee arthroplasty (TKA). It will evaluate the effectiveness of a brief preoperative mindfulness session and an intensive 8-week mindfulness program in improving postoperative musculoskeletal health and reducing chronic opioid use. The study will also identify patient characteristics that influence the effectiveness of these interventions. Conducted across multiple Military Health System sites, it seeks to enhance recovery outcomes for TKA patients.
Why it matters
Potential benefit: If successful, this study could significantly improve recovery and reduce opioid dependence for military patients after knee surgery.
How similar studies have gone: Other studies have shown promise in using mindfulness interventions for pain management, suggesting potential success for this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Scheduled to undergo unilateral total TKA at one of the study sites * TRICARE beneficiary * Facility with the English language that is adequate to complete study procedures. Exclusion Criteria: * Cognitive impairment preventing completion of study procedures, * Formal mindfulness training (e.g., MBSR, MBCT) * Severe, active suicidality * Contralateral TKA in the past 3 months or planned contralateral TKA during the study * Current cancer diagnoses.
Where it's running
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Brooke Army Medical Center
Fort Sam Houston, Texas, United States Recruiting
Study contacts
- Study coordinator: Rachel Mayhew
- Email: rachel.j.mayhew.ctr@mail.mil
- Phone: 253.968.2911
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.