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Behavioral Intervention
Music Intervention for Chronic Pain (MusicCPP Trial)
Québec, Canada
N/A
Recruiting
Led By Anne Marie Pinard, Md, MA
Research Sponsored by Laval University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Have satisfactory or corrected hearing;
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up the posttest was administered 25 minutes after the pretest.
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to see if personalized music can help people with chronic pain feel better. They will measure if the music program reduces pain, anxiety, and improves well-being using a scale called ESAS-r
See full description
Who is the study for?
This trial is for adults over 18 who suffer from chronic pain, are currently being treated at the CHU de Québec-Université Laval's pain clinic, can use email and online questionnaires, have good or corrected hearing, understand French, and can travel to Université Laval.Check my eligibility
What is being tested?
The study tests a personalized music intervention program on individuals with chronic pain. It aims to see if this program reduces their composite score of pain and anxiety while improving well-being more than control sessions do.See study design
What are the potential side effects?
Since this trial involves a non-invasive music intervention rather than medication or surgery, there are no direct physical side effects expected. However, individual emotional responses to music may vary.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My hearing is good or corrected to normal.
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Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ the posttest was administered 25 minutes after the pretest
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~the posttest was administered 25 minutes after the pretest
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Changes in Composite pain, anxiety, and well-being (reversed) score
Secondary study objectives
Changes in Anxiety levels
Changes in Pain levels
Changes in well-being (reversed)
Other study objectives
Subjective experience
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Musical interventionExperimental Treatment1 Intervention
This arm will receive a personalized music intervention.
Group II: No musical interventionActive Control1 Intervention
This arm will carry out its daily activities and will be assessed using the same measures at the beginning of each session and after a delay comparable to the duration of the intervention administered in the experimental group.
Find a Location
Closest Location:Pavillon Louis-Jacques-Casault· Québec, Canada
Who is running the clinical trial?
Laval UniversityLead Sponsor
438 Previous Clinical Trials
177,686 Total Patients Enrolled
1 Trials studying Chronic Pain
86 Patients Enrolled for Chronic Pain
Université de MontréalOTHER
222 Previous Clinical Trials
104,329 Total Patients Enrolled
Anne Marie Pinard, Md, MAPrincipal InvestigatorCIRRIS