Mind-Body JRA: Psychosocial Support for Pre-operative Pain and Distress

Sponsor
University of Utah (Other)
Overall Status
Completed
CT.gov ID
NCT03665727
Collaborator
(none)
727
1
4
15.6
46.5

Study Details

Study Description

Brief Summary

The purpose of this randomized study is to determine the impact of three different types of psychosocial support delivered by mental health professionals to pre-operative joint replacement patients. This study will examine the differential effects of brief mindfulness training, hypnostic suggestion, and cognitive behavioral pain psychoeducation for pre-operative patients, with a supplemental nonrandomized usual care comparison group.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Mindfulness
  • Behavioral: Suggestion
  • Behavioral: Psychoeducation
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
727 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Masking Description:
Clinical assessors were masked at postoperative follow-up
Primary Purpose:
Treatment
Official Title:
Psychosocial Support for Pre-operative Pain and Distress
Actual Study Start Date :
Jun 4, 2018
Actual Primary Completion Date :
Sep 23, 2019
Actual Study Completion Date :
Sep 23, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Mindfulness

15 minute mindfulness session

Behavioral: Mindfulness
The 15 minute mindfulness session is a scripted mindfulness exercise that incorporates mindfulness principles of intentionally paying attention to present-moment experience in a non-judgmental fashion.

Experimental: Suggestion

15 minute therapeutic suggestion session

Behavioral: Suggestion
The 15 minute suggestion session is a scripted suggestion exercise that incorporates imagery and suggestions for changes in cognition, emotion, and body sensations.

Active Comparator: Psychoeducation

15 minute psychoeducation session

Behavioral: Psychoeducation
The 15 minute psychoeducation session is a supportive session in which behavioral coping strategies for pain management are discussed.

No Intervention: Usual Care

The usual care comparison group was comprised of patients who underwent total joint arthroplasty of the hip or knee at the same academic medical center during the study period but who did not attend Joint Academy.

Outcome Measures

Primary Outcome Measures

  1. Pain Intensity Numeric Rating Scale [Immediately prior to and following intervention]

    Single Likert scale item ranging from 0-10, with 0 indicating no pain and 10 representing the most intense pain imaginable.

  2. Pain Unpleasantness Numeric Rating Scale [Immediately prior to and following intervention]

    Single Likert scale item ranging from 0-10, with 0 indicating no pain and 10 representing the most unpleasant pain imaginable.

Secondary Outcome Measures

  1. Pain Medication Desire Numeric Rating Scale [Immediately prior to and following intervention]

    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.

  2. Anxiety Numeric Rating Scale [Immediately prior to and following intervention]

    Single Likert scale item ranging from 0-10, with 0 indicating no anxiety and 10 representing very anxious.

  3. Postoperative Patient Reported Outcomes Measurement Information System (PROMIS) Physical Functioning Item Bank, v2.0 [During the 6 weeks prioir 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.

  4. Nondual Awareness Dimensional Assessment - State [Immediately prior to and following intervention]

    Three Likert scale item ranging from 0-30, with 0 indicating no nondual awareness and 10 representing complete nondual awareness. Items can also be used individually. Item one is a single Likert scale item ranging from 0-10, with 0 indicating no relational unity and 10 representing complete relational unity. Item two is a single Likert scale item ranging from 0-10, with 0 indicating no annihilational unity and 10 representing complete annihilational unity. Item three is a single Likert scale item ranging from 0-10, with 0 indicating no bliss and 10 representing complete bliss.

  5. Sensation Manikin Body Sensation Report [Immediately prior to and following intervention]

    The ratio of pleasant to unpleasant bodily sensations reported on a sensation manikin. Ratio scores below 1 indicate unpleasant sensations predominate in the body and ratio scores above 1 indicate pleasant scores predominate.

Other Outcome Measures

  1. Present Moment Awareness Numeric Rating Scale (Manipulation Check) [Immediately prior to and following intervention]

    Single Likert scale item ranging from 0-10, with 0 indicating no awareness of the present and 10 representing complete awareness of the present moment.

  2. Decentering Numeric Rating Scale (Manipulation Check) [Immediately prior to and following intervention]

    Single Likert scale item ranging from 0-10, with 0 indicating no decentering and 10 representing a completely decentered perspective.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • English-speaking males or females

  • 18 years old or older

  • patients within the University of Utah Hospital system

  • patients attending the Joint Replacement Academy to prepare for either hip or knee replacement surgery

Exclusion Criteria:
  • Altered mental status due to delirium, psychosis, or pharmacological sedation as determined by clinical assessment.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Utah Salt Lake City Utah United States 84112

Sponsors and Collaborators

  • University of Utah

Investigators

None specified.

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
Eric Garland, Associate Dean for Research College of Social Work Director; Center on Mindfulness and Integrative Health Intervention Development (C-MIIND), University of Utah
ClinicalTrials.gov Identifier:
NCT03665727
Other Study ID Numbers:
  • IRB_00085446
First Posted:
Sep 11, 2018
Last Update Posted:
May 27, 2020
Last Verified:
May 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 27, 2020