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Brief Nurse-led Mindfulness Based Intervention

Not Applicable
Completed
Conditions
Osteoarthritis, Hip
Pain
Osteoarthritis, Knee
Interventions
Behavioral: Nurse-led Pain Psychoeducation
Behavioral: 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
Inclusion Criteria
    1. Age ≥18,
    1. Scheduled to undergo unilateral total knee arthroplasty
Exclusion Criteria
    1. Cognitive impairment preventing completion of study procedures.
    1. Current cancer diagnosis,
    1. Contralateral knee replaced in the previous 3 months,
    1. Intent to have contralateral knee replaced or other, additional surgical procedure during the study period,
    1. Intent to add new pain treatments during the study period (except for what is part of the study),
    1. Other unstable illness judged by medical staff to interfere with study treatment.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Nurse-led Pain PsychoeducationNurse-led Pain Psychoeducation-
Nurse-led Mindfulness Based InterventionNurse-led Pain Psychoeducation-
Nurse-led Mindfulness Based InterventionNurse-led Mindfulness Based Intervention-
Primary Outcome Measures
NameTimeMethod
Change in Pain Intensity Numeric Rating Scalebaseline 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
NameTimeMethod
Postoperative Patient Reported Outcomes Measurement Information System (PROMIS) Physical Functioning Item Bank, v2.0During 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 Scalebaseline 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 Scalebaseline 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

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