Effectiveness of Musicotherapy in Reducing Pain Induced by Leg Ulcer Care (MUS-ICAT)

University Hospital Center of Martinique

Status: Enrolling

Conditions: Leg Ulcers Venous; Debridement Care; Pain; Leg Ulcer

Treatments: Other: Musicotherapy

Study type: Interventional

Funder types: Other

Identifiers

NCT06153589

23_RIPH2-10

Details and patient eligibility

About

Venous leg ulcer is the final stage of chronic venous disease and only develops due to advanced chronic venous insufficiency. The problems caused by venous disease are initially minor and often neglected, but can impact the quality of life of patients.

The prevalence of leg ulcers is estimated at 1% of the general population and 3% to 5% of subjects over 65 years old. Its prevalence increases with age in both men and women.

Managing chronic ulcers requires a certain number of care procedures, including debridement.

The act of treatment by mechanical debridement is little relieved by the analgesics given beforehand, and can be painful, with risks of bleeding.

Musicotherapy, particularly the U-shaped method, has shown its effectiveness in the treatment of pain and anxiety in several areas (geriatrics, intensive care, rheumatology, oncology, etc.).

The standardized musicotherapy method of the U-shaped sequence was developed and initially evaluated by clinical studies coordinated by the INSERM unit U1061 (Pr. Jacques Touchon; Dr. Stéphane Guétin).

Following the publication of numerous controlled, randomized studies presenting results on the effectiveness in the treatment of pain and anxiety, a digital application was developed in order to standardize the method. The Music Care health application is now a Class 1 Medical Device, with CE marking obtained.

This "U-shaped sequence" is standardized and has been clinically validated, which makes Music Care a unique tool available for pain relief.

No studies have been found in the literature regarding the use of music therapy during debridement care.

Enrollment: 180 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult patient,

• Patient followed at the M@diCICAT healing center requiring wound debridement :

  • For a venous or arterial ulcer or necrotizing angiodermatitis of the lower limbs,
  • Having the ability to verbalize about their pain (communicating),
  • With a planned debridement time of less than 40 minutes.

• Patient affiliated to or beneficiary of a social security scheme,

• Patient having given free, informed and express consent.

Exclusion criteria

• Patient with a diabetic foot (loss of sensitivity-neuropathy),
• Patient not requiring a debridement session,
• Patient with an infected ulcer (abscess, etc.),
• Patient with critical ischemia,
• Patient with hearing problems,
• Patient with cognitive disorders,
• Patient placed under legal protection, guardianship or curatorship,
• Pregnant or breastfeeding woman.

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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180 participants in 2 patient groups

Musicotherapy + debridement and usual analgesic protocol

Experimental group

Description:

Patients in the experimental arm will receive classic debridement care and usual use of analgesic treatment, accompanied by a musicotherapy session respecting the standardized method of the U-shaped sequence.

Treatment:

Other: Musicotherapy

Debridement and usual analgesic protocol

No Intervention group

Description:

Patients in the experimental arm will receive classic debridement care and usual use of analgesic treatment.