Do Inflammatory Arthritis Inpatients Receiving Group Music Therapy Improve Pain Compared to Music Listening?

January 9, 2019 updated by: Katherine Wright, University of British Columbia

Do Inflammatory Arthritis Inpatients Receiving Group Music Therapy Improve Pain Compared to Music Listening Over the 4 Weeks Using a Randomised Control Trial?

Pain management is rated by patients with inflammatory arthritis as the highest priority in their disease treatment. Past research showed that music therapy is associated with reduced pain and depression. The purpose of this study is to better understand the effectiveness of music therapy for people with inflammatory arthritis. Participants will be randomly assigned to: 1) Music Therapy group facilitated by a music therapist, or 2) Music Listening group that listens to a relaxation CD (compact disc). Standardized tests will determine if participating in music therapy group helps reduce pain and depression, improve physical function and confidence levels in applying self-management strategies.

Study Overview

Detailed Description

  1. Purpose:

    To better understand the effectiveness of music therapy for people with inflammatory arthritis. Determine if participating in a music therapy group facilitated by a music therapist helps reduce pain and depression, and improve physical function and self-efficacy.

    No optional studies are currently planned.

  2. Hypothesis Participants in the Music Therapy group will report less pain than those in the Music Listening group after the intervention phase. Music Therapy will also be associated with improvement in secondary outcomes including physical functioning, self-efficacy, and depression.
  3. Justification G F Strong Rehabilitation Center Arthritis Inpatient Program has an interdisciplinary approach to pain management: education, medical management, physiotherapy interventions such as exercises and use of physical agents (i.e. heat, cold, electrotherapy, ultrasound), occupational therapy intervention (i.e. activity modification and use of adaptive devices), and social work, dietician, psychology and pharmacy services. Current standard of care has limitations; it insufficiently addresses emotional aspects of chronic pain management. It also introduces relaxation strategies in a didactic module but does not provide training and opportunity to practice these strategies with the support of a health care professional. The Music Therapy intervention group is facilitated by a music therapist. Music therapists are trained to manipulate elements of music to achieve desired effects during music therapy interventions. These elements, such as beat, tempo (speed), or pitch level, can trigger adaptive neurophysiological, psychophysiological, emotional and behavioural responses. The Music Therapy group offers a chance to practice pain management and relaxation strategies, increase a sense of social cohesion and reduce a sense of isolation that individuals may experience when dealing with chronic pain. Participants in the control Music Listening group will listen to a relaxation CD.

    Past research showed that music therapy and music listening are associated with reduced pain intensity levels, increased functional mobility, and reduced depression. There was no clear research found on group music therapy's effectiveness on people with inflammatory arthritis. This feasibility study will help to better understand the effectiveness of music therapy for people with inflammatory arthritis.

  4. Objectives

    Outcome measures to be collected include:

    • Category Rating Scale for Pain (from RAPID-3)
    • Rheumatoid Arthritis Self-efficacy Scale (RASE)
    • 6 Minute Walk Test (6MWT)
    • Routine Assessment of Patient Index Data 3 (RAPID-3)
    • Canadian Occupational Performance Measures (COPM)
    • Center for Epidemiological Studies Depression Scale (CES-D) Data will be collected on three occasions: 1) time of enrollment, 2) after attending Music Therapy or Music Listening sessions, and 3) one month after completion of intervention.
  5. Research Method

    • Target population: patients with inflammatory arthritis admitted to G F Strong Rehabilitation Center Inpatient Arthritis program
    • Sampling method: participants will be stratified into 4 groups and randomized using a 1:1 allocation ratio into 2 groups: Music Therapy and Music Listening. 40 patients are expected to enroll during recruiting time from April to September in 2015.
    • Research design: Parallel group feasibility randomized controlled trial with a dose-matched active comparator.
  6. Statistical Analysis Statistical software such as R, Minitab and Cytel Studio will be used to create descriptive statistics such as means and standard deviations; medians and interquartile ranges, minima, and maxima. A CONSORT flow chart will be constructed to show any losses during the trial, and imputation methods will be used to study the impact of missingness on any of the estimates and conclusions. Statistical models for each outcome variable will be used to measure the effect of Music Therapy compared to Music Listening group. Model assumptions such as independence of observations, normality of residuals and homogeneity of variance to validate the statistical analyses will be conducted.

Study Type

Interventional

Enrollment (Actual)

13

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • British Columbia
      • Vancouver, British Columbia, Canada, V5Z 2G9
        • G F Strong Rehabilitation Centre

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years to 85 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Diagnosis of inflammatory arthritis
  2. Admission to G F Strong Rehabilitation Center Arthritis Inpatient Program from the community or after joint replacement surgery
  3. Between ages 16 and 85 years
  4. Can speak, read and write in English

Exclusion Criteria:

  1. Self-reported hearing loss
  2. Clinician judgement of being unable to follow directions

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Music Therapy
The music therapy group will run for approximately an hour (twice a week) and will involve in-vivo relaxation where the live music is manipulated in terms of speed and intensity to bring on a state of relaxation. There will be a brief therapist-led discussion before and after the relaxation portion to increase a sense of group cohesion. Procedures that will be used are based on evidence-based practice for trained Music Therapists.
In-vivo relaxation where the live music is manipulated in terms of speed and intensity to bring on a state of relaxation for approximately an hour. There will be a brief therapist-led discussion before and after the relaxation portion to increase a sense of group cohesion. Procedures that will be used are based on evidence-based practice for trained Music Therapists.
Active Comparator: Music Listening
The control group will also run for approximately an hour (twice a week) and will involve listening to relaxing music on a CD player.
Listening to relaxing music on a CD player for approximately an hour.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain Scale rating (on Routine Assessment of Patient Index Data 3)
Time Frame: after attending 8 Music Therapy or Music Listening sessions over 4 weeks
Numeric pain rating from 0 to 10 with 0.5 increment
after attending 8 Music Therapy or Music Listening sessions over 4 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Rheumatoid Arthritis Self-efficacy Scale (RASE)
Time Frame: after attending 8 Music Therapy or Music Listening sessions over 4 weeks
Self-reported questionnaire rating on self-efficacy in the areas of pain management, fatigue management, stress management, joint protection and management of activities of daily living.
after attending 8 Music Therapy or Music Listening sessions over 4 weeks
6 Minute Walk Test (6MWT)
Time Frame: after attending 8 Music Therapy or Music Listening sessions over 4 weeks
Objective measurement of walking endurance in 6 minutes.
after attending 8 Music Therapy or Music Listening sessions over 4 weeks
Routine Assessment of Patient Index Data 3 (RAPID-3)
Time Frame: after attending 8 Music Therapy or Music Listening sessions over 4 weeks
Subjective questionnaire on performance level of activities of daily living.
after attending 8 Music Therapy or Music Listening sessions over 4 weeks
Canadian Occupational Performance Measures (COPM)
Time Frame: after attending 8 Music Therapy or Music Listening sessions over 4 weeks
Subjective report on performance level of activities of daily living and self reported satisfaction level
after attending 8 Music Therapy or Music Listening sessions over 4 weeks
Center for Epidemiological Studies Depression Scale (CES-D)
Time Frame: after attending 8 Music Therapy or Music Listening sessions over 4 weeks
self reported questionnaire on frequency of experiencing depression symptoms.
after attending 8 Music Therapy or Music Listening sessions over 4 weeks
Pain Scale rating (on Routine Assessment of Patient Index Data 3)
Time Frame: one month after completion of intervention
Numeric pain rating from 0 to 10 with 0.5 increment
one month after completion of intervention
Rheumatoid Arthritis Self-efficacy Scale (RASE)
Time Frame: one month after completion of intervention
Self-reported questionnaire rating on self-efficacy in the areas of pain
one month after completion of intervention
6 Minute Walk Test (6MWT)
Time Frame: one month after completion of intervention
Objective measurement of walking endurance in 6 minutes.
one month after completion of intervention
Routine Assessment of Patient Index Data 3 (RAPID-3)
Time Frame: one month after completion of intervention
Subjective questionnaire on performance level of activities of daily living.
one month after completion of intervention
Canadian Occupational Performance Measures (COPM)
Time Frame: one month after completion of intervention
self reported questionnaire on frequency of experiencing depression symptoms.
one month after completion of intervention
Center for Epidemiological Studies Depression Scale (CES-D)
Time Frame: one month after completion of intervention
self reported questionnaire on frequency of experiencing depression symptoms.
one month after completion of intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Katherine M Wright, MA, G F Strong

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 6, 2015

Primary Completion (Actual)

December 31, 2017

Study Completion (Actual)

January 31, 2018

Study Registration Dates

First Submitted

April 8, 2015

First Submitted That Met QC Criteria

May 4, 2015

First Posted (Estimate)

May 7, 2015

Study Record Updates

Last Update Posted (Actual)

January 11, 2019

Last Update Submitted That Met QC Criteria

January 9, 2019

Last Verified

January 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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