The Effect of Preferred Music on EMG Anxiety and Pain

Sponsor
Lawson Health Research Institute (Other)
Overall Status
Unknown status
CT.gov ID
NCT03610503
Collaborator
(none)
90
1
2
23.4
3.8

Study Details

Study Description

Brief Summary

Patients often report anxiety and pain related to electromyography (EMG) and nerve conduction studies (NCS) which are tests used to look for diseases of the nerves and muscles. Unfortunately, for those with very high levels of test related stress, the experience may be very frightening and may impede completion of the study and negatively impact on making a timely and accurate diagnosis. Several studies have shown that music can improve anxiety and pain levels in various situations and procedures. Our study will allow participants to play music of their choice during EMG and NCS in order to determine if the pain and anxiety that they experience is reduced.

Condition or Disease Intervention/Treatment Phase
  • Other: Music
N/A

Detailed Description

This study will be a prospective randomized trial carried out at Mount Hope Centre for Long Term Care in London, Ontario. All patients referred for electromyography and a nerve conduction study will be considered for inclusion in the study. Those who meet the criteria and verbally consent to the study will sign a consent form and then be randomly assigned to either a music or no-music group using a computer-generated random number series. Prior to starting the test, all participants who enroll in the study will complete form Y-1 and Y-2 of the state-trait anxiety inventory (STAI) which measure state (S) anxiety and trait (T) anxiety respectively. They will also complete an 100 mm visual analogue scale (VAS) for pain and anxiety prior to beginning the studies. During and following the test they will be asked to complete a VAS for pain and anxiety, and the Y-1 of the STAI to measure state anxiety. Aside from having to fill out the STAI and visual analogue scales, patients assigned to the no-music group will undergo the EMG and NCS as per usual. Those in the music group will be given a set of over-ear headphones (sterilized before use) and a tablet device. Participants will be allowed to navigate Spotify, a digital music service to select whatever music they desire. An app that limits volume will be used to ensure that volume cannot be raised above 80 decibels by the patient. Communication with the patient will not be hindered as the EMG technician and physician will be speaking into a microphone that transmits the sound directly to the participant's headphones.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
90 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized, intervention-control, trialRandomized, intervention-control, trial
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Masking Description:
Anonymous data collection to be reviewed
Primary Purpose:
Prevention
Official Title:
The Effect of Preferred Music on Anxiety and Pain in Electrodiagnostic Studies: A Prospective Randomized Trial
Actual Study Start Date :
Aug 20, 2018
Anticipated Primary Completion Date :
Dec 1, 2019
Anticipated Study Completion Date :
Aug 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Music

Patients listen to music during EMG test

Other: Music
Participants in this arm will listen to music during the EMG testing

No Intervention: Control (Standard Care)

Patients do not listen to music during EMG test (ie. Standard of care)

Outcome Measures

Primary Outcome Measures

  1. State-trait anxiety inventory (STAI) [Change in STAI (State sub-scale) from immediately before the EMG procedure, during the EMG procedure and immediately after EMG procedure]

    Anxiety inventory that measures both Trait (T) and State (S) anxiety. Each sub- scale (T and S) is measured from 20-80 and reported individually (not combined) with higher values indicating higher anxiety. The typical cut off for S sub-scale is a score greater than 40 indicating clinically significant symptoms.

Secondary Outcome Measures

  1. Visual analog scale (VAS) for pain and anxiety scale (0-100) [Change in VAS immediately before the EMG procedure, during the EMG procedure, and immediately after EMG procedure]

    Pain and anxiety scale using a standard VAS (0 = No pain/anxiety, 100 = maximal).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients 18 years of age or older referred for NCS and EMG at Mount Hope Centre for Long Term Care in London, Ontario will be eligible and offered entry into the study if the following criteria are met: the NCS/EMG are indicated, they have at least a 6th grade reading level in English such that they can complete the STAI, and the patient is willing and able to provide signed informed consent.
Exclusion Criteria:
  1. Use of hearing aids that would preclude or hinder the use of over-ear headphones.

  2. Profound hearing loss.

  3. Cognitive Impairment

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mount Hope EMG Lab, St. Joseph's Health Care (SJHC) London Ontario Canada N6A 1Y6

Sponsors and Collaborators

  • Lawson Health Research Institute

Investigators

  • Principal Investigator: Steven Macaluso, M.D., Schulich School of Medicine and Dentistry

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lawson Health Research Institute
ClinicalTrials.gov Identifier:
NCT03610503
Other Study ID Numbers:
  • REDA 5189
First Posted:
Aug 1, 2018
Last Update Posted:
Mar 14, 2019
Last Verified:
Mar 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
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 Mar 14, 2019