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Recruiting NCT07459855

This is a Study to Find Out Whether Music Therapy Can Reduce Stress During Wound Care

No phase Interventional Wound Surgical

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: music.
Who it may be relevant to
Registry conditions: Wound Surgical. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Switzerland
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Music Therapy to Reduce Stress and Increase Satisfaction in Patients Undergoing Surgical Wound Dressings in the In-hospital Setting: a Randomized Study

Overview

This study involves hospitalized patients who need wound dressing procedures. Patients will be assigned by chance to one of two groups. One group will listen to music of their choice during wound care, while the other group will receive standard wound care without music. The investigators will then compare the two groups to see whether listening to music helps reduce stress and improve the experience during the procedure.

Interventions

  • Other music
    patient-selected music

Primary outcome measures

  • change in heart rate [Time frame: periprocedural]
Secondary outcome measures (5)
  • change in blood pressure [Time frame: periprocedural]
  • change in respiratory rate [Time frame: periprocedural]
  • change in oxygen saturation [Time frame: periprocedural]
  • pain intensity [Time frame: periprocedural]
  • perceived anxiety [Time frame: periprocedural]

Eligibility criteria

Inclusion criteria

  • Hospitalized patients undergoing wound dressing procedures
  • Age ≥ 18 years

Exclusion criteria

  • Pregnant or lactating women
  • Cognitive impairment or language barriers
  • Severe hearing impairment
  • Clinical instability requiring urgent medical intervention at the time of wound dressing

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Other

Study locations

Switzerland · 1 center
  • Ospedale Regionale Bellinzona e Valli, Ente Ospedaliero Cantonale — Bellinzona

Identifiers

NCT: NCT07459855 · ORBV-CHIR-009

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗