Brief Nurse-led Mindfulness Based Intervention
- Conditions
- Osteoarthritis, HipPainOsteoarthritis, Knee
- Interventions
- Behavioral: Nurse-led Pain PsychoeducationBehavioral: Nurse-led Mindfulness Based Intervention
- Registration Number
- NCT04800354
- Lead Sponsor
- University of Utah
- Brief Summary
This is a single-site, two-arm, parallel-group randomized clinical trial (RCT). The feasibility, acceptability, and clinical effects of the nurse-led, very brief, preoperative mindfulness based intervention for hip and knee replacement patients will be investigated relative to nurse-led preoperative pain psychoeducation.
A secondary sub-analysis will compare two different styles of mindfulness practice (mindfulness of breath vs. mindfulness of pain) relative to preoperative pain psychoeducation.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 127
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- Age ≥18,
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- Scheduled to undergo unilateral total knee arthroplasty
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- Cognitive impairment preventing completion of study procedures.
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- Current cancer diagnosis,
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- Contralateral knee replaced in the previous 3 months,
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- Intent to have contralateral knee replaced or other, additional surgical procedure during the study period,
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- Intent to add new pain treatments during the study period (except for what is part of the study),
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- Other unstable illness judged by medical staff to interfere with study treatment.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Nurse-led Pain Psychoeducation Nurse-led Pain Psychoeducation - Nurse-led Mindfulness Based Intervention Nurse-led Pain Psychoeducation - Nurse-led Mindfulness Based Intervention Nurse-led Mindfulness Based Intervention -
- Primary Outcome Measures
Name Time Method Change in Pain Intensity Numeric Rating Scale baseline and after the 15 minute preoperative nurse visit Single Likert scale item ranging from 0-10, with 0 indicating no pain and 10 representing the most intense pain imaginable.
- Secondary Outcome Measures
Name Time Method Postoperative Patient Reported Outcomes Measurement Information System (PROMIS) Physical Functioning Item Bank, v2.0 During the 6 weeks prior to surgery and at the 6-week outpatient follow-up appointment The PROMIS physical functioning computer assisted test draws from a bank of 123 items all scored on a 5 point Likert scale.
T-Score distributions are standardized such that a 50 represents the average (mean) for the US general population, and the standard deviation around that mean is 10 points. A high score better physical functioning.Change in Pain Unpleasantness Numeric Rating Scale baseline and after the 15 minute preoperative nurse visit Single Likert scale item ranging from 0-10, with 0 indicating no pain and 10 representing the most unpleasant pain imaginable.
Change in Pain Medication Desire Numeric Rating Scale baseline and after the 15 minute preoperative nurse visit Single Likert scale item ranging from 0-10, with 0 indicating no desire for pain medication and 10 representing a strong desire for pain medication.
Trial Locations
- Locations (1)
University of Utah
🇺🇸Salt Lake City, Utah, United States