Music Intervention to Reduce Anxiety and Prevent Delirium in Older Adults Undergoing Cardiac Surgery

NCT ID
NCT07851194
Registry status
Not yet recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
KU Leuven
Conditions
Cardiac Surgery, Postoperative Delirium, Preoperative Anxiety

Overview

ClinicalTrials.gov lists this study as Not yet recruiting.

Official title: Music Intervention for rEduction of Preoperative Anxiety and Prevention of Postoperative deLirium in Older aDults Undergoing Cardiac surgerY

Enrollment: 256 participants (Estimated).

What is being studied

  • Other: Music Intervention Group

Who may be eligible

Ages
65 Years to no maximum
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * Voluntary written informed consent of the participant or the participant's legally authorized representative has been obtained prior to any screening procedures * At least 65 years of age at the time of signing the Informed Consent Form (ICF) * Scheduled for elective cardiac surgery. * Able to participate and communicate in Dutch. Exclusion Criteria: * Participant has a history of music-induced seizures. * Inability to use headphones or smartphones. * Deafness or severe hearing impairment, defined as being unable to listen to music. * Presence of delirium at baseline, as screened with the 3-Minute Diagnostic Interview for Confusion Assessment Method (3D-CAM). * Disabling neurological diseases, including stroke, dementia, and active epilepsy (requiring ongoing anti-epileptic medication). * Current treatment with anxiolytics, antidepressants, or antipsychotics. * Admission on the day of surgery. * Expected postoperative intensive care unit (ICU) admission longer than one day. * Participation in an interventional study with an investigational medicinal product (IMP) or device.

Study locations

1 study location is listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: Belgium

  • Vlaams-Brabant, Belgium: 1

Sample of listed locations

  • University Hospital Leuven — Leuven, Vlaams-Brabant, 3000, Belgium — Site recruitment status not specified in the registry data

Study details

Start date
October 1, 2026
Primary completion date
March 28, 2028
Completion date
April 15, 2028
First posted
October 1, 2026

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07851194
Registry last updated
October 1, 2026
QualifiedStudies registry data refreshed
October 5, 2026
QualifiedStudies record fetched
October 5, 2026

View NCT07851194 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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