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The Feasibility and Acceptability of a Music Intervention to Reduce Preoperative Anxiety in Older Patients

NCT06173674 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 78

Last updated 2024-08-22

No results posted yet for this study

Summary

The goal of this clinical feasibility study is to learn about the acceptability and feasibility of a music intervention in older patients undergoing cardiac surgery and Transcatheter Aortic Valve Implantation (TAVI) procedure.

The primary question it aims to answer is:

• What is the feasibility and acceptability of a music intervention to reduce PA in older patients undergoing cardiac surgery and TAVI?

The secondary question is:

• What is the effect of a music intervention on PA levels and the incidence of POD in older patients undergoing cardiac surgery and TAVI?

Participants will

* listen to music before the surgery/TAVI procedure
* be evaluated for preoperative anxiety levels and postoperative delirium
* be interviewed to learn about their perspectives regarding the music intervention

Conditions

  • Preoperative Care
  • Preoperative Anxiety

Interventions

OTHER

Music intervention

The music intervention will consist of three components including: 1. Playlist composition Six music genres playlists will be offered to patients, including Classical Music, Country Music, Folk Music, Hymns and Reglious Music, Jazz and Swing Music, Popular/Easy Listening/RNB and Soundtrack Music. Patients can also add their favourite music to the list as well. 2. Music Intervention Delivery The general criteria for intervention delivery are:1) Each session lasts at least 20 minutes; 2) The music will be delivered by a comfortable, wireless, on/off switch noise-cancelling headphone; 3) The volume will be adjusted according to the patient's preference and controlled at 65dB or lower; 4) The order of music in the playlists will be decided by the patient; 5) Music will be delivered in inpatient room and/or waiting area before surgery/procedure. 3. Cleaning and infection of the equipment We will comply with guidelines on disinfection of materials in the hospital.

Sponsors & Collaborators

  • KU Leuven

    lead OTHER

Principal Investigators

  • Koen Milisen, PhD · Department of Public Health and Primary Care, Academic Centre for Nursing and Midwifery, KU Leuven

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-12-04
Primary Completion
2024-04-15
Completion
2024-04-15

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06173674 on ClinicalTrials.gov