What this study is
The overarching objective of this proposal is to conduct a multi-site Sequential Multiple Assignment Randomized Trial (SMART) across multiple Military Health System (MHS) sites to optimize the sequencing and integration of two intervention strategies in total knee arthoplasty (TKA) patients: a single-session mindfulness-based intervention (MBI) and an intensive 8-week MBI-Mindfulness-Oriented Recovery Enhancement (MORE) designed to simultaneously reduce prolonged pain and chronic opioid use by enhancing self-regulation. Aim 1: Evaluate the extent to which a brief preoperative MBI improves TKA patients' postoperative musculoskeletal health and reduces chronic opioid use. Aim 2: Evaluate the extent to which an intensive MBI (MORE) improves musculoskeletal health and reduces chronic opioid use among patients non-responsive to preoperative intervention. Aim 3: (A) Determine patient baseline characteristics that moderate MBI treatment responses. (B) Quantify the degree to which the impact of Phase 1 and 2 MBIs on musculoskeletal health and opioid dose are mediated by changes in mechanistic autonomic marker of self-regulation: heart-rate variability (HRV).
What's being tested
- Brief mindfulness
Intervention · BEHAVIORAL
A 15-minute guided mindfulness practice that includes focused attention on breath and body sensations and open monitoring and acceptance of thoughts, emotions, and pain.
- Mindfulness-Oriented Recovery Enhancement (MORE)
Intervention · BEHAVIORAL
An 8-session intervention. Sessions involve: 1) mindfulness training to reduce pain and increase self-regulation over opioid use, 2) cognitive reappraisal to decrease psychological distress, and 3) savoring to augment natural reward processing, positive emotion, and esprit de corps.
- Standard care
Intervention · OTHER
Preoperative Standard Care. Patients will attend a 2-hour preoperative class involving pain coping education and are offered prehabilitation services. Postoperative standard care includes (1) pain medications to minimize opioid use, including acetaminophen, lyrica, meloxicam/naproxen and celebrex, and (2) anticoagulants for 3-6 weeks postoperatively, as well as (3) ambulatory care with assistive devices 1-6 weeks after surgery. Patients see their surgeon postoperatively 2-6 weeks after surgery, 3-6 months, and yearly.
Study details
- Sponsor
- University of Utah
- Conditions
- Knee Pain Chronic
- Enrolling
- 500 people
- Starts
- 2022-05-01
- Est. completion
- 2027-10
- Design
- Triple-blind, randomized, sequential groups
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years and overSex ALLHealthy volunteers Not acceptedYou may qualify if
- 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.
You can't join if
- 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.
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openBrooke Army Medical Center
Fort Sam Houston, Texas, United States
- Tina Greenlee · ContactTtgreenlee@genevausa.org
Recruiting
Study team
Sponsor
University of Utah
Study ID DOD02
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.