Feasibility and Efficacy of Music Intervention on Pain, Anxiety, and Well-being in Chronic Pain Patients

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this randomized controlled trial is to evaluate the efficacy of a personalized music intervention program to improve the condition of individuals suffering from chronic pain. The main objective is to evaluate if the intervention program will significantly reduce participants composite score of pain, anxiety, and well-being (reversed) as evaluated by the Edmonton symptom assessment scale (ESAS-r) immediately after the intervention, and whether this improvement will be significantly greater than that of control sessions.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Aged 18 years and older;

• Suffering from chronic pain and actively attending the pain clinic at the CHU de Québec-Université Laval;

• Have an email and be able to respond to online questionnaires using a computer, tablet, or phone;

• Have satisfactory or corrected hearing;

• Understand French;

• Be able to travel to Université Laval.

Locations
Other Locations
Canada
Pavillon Louis-Jacques-Casault
RECRUITING
Québec
Contact Information
Primary
Josiane Bissonnette, Ph.D.
josiane.bissonnette@mus.ulaval.ca
418-656-2131
Backup
Anne Marie Pinard, Md, MA
anne-marie.pinard@fmed.ulaval.ca
418 656-2131
Time Frame
Start Date: 2024-05-28
Estimated Completion Date: 2025-12
Participants
Target number of participants: 36
Treatments
Experimental: Musical intervention
This arm will receive a personalized music intervention.
No_intervention: No musical 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.
Related Therapeutic Areas
Sponsors
Collaborators: Université de Montréal
Leads: Laval University

This content was sourced from clinicaltrials.gov