RECRUITING

Listening to Calming Music

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinical trial is to explore possible benefits and mechanisms through which listening to music can improve health and wellness. The main goals of the study are: * To investigate whether pre-survey measures of autonomic reactivity relate to the overall functioning of participants. * To examine the immediate effects of listening to the augmented music. * To identify individual characteristics that influence the immediate effects of listening to the augmented music. Participants will: PHASE 1: * Complete the online pre- and post-surveys * Listen to the brief music demo * Listen to the full 15-minutes music session PHASE 2: * Complete the online pre- and post-surveys. * Heart rate data will be collected continuously for about 25 minutes. It will be collected for 5 minutes before and after the intervention, and for 15 minutes during the intervention. * Provide pre- and post- music saliva samples (1.5mL). * Listen to full 15-minutes music session.

Official Title

The Effect of Listening to Calming Music

Quick Facts

Study Start:2024-12-04
Study Completion:2025-09-25
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06710886

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 89 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Between the ages of 18 and 89
  2. * Proficient in English
  3. * Attendees of an online workshop session
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Lourdes P Dale, PhD
CONTACT
9042448998
Lourdes.Dale@jax.ufl.edu
Audrey N Dana
CONTACT
audrey.dana@jax.ufl.edu

Principal Investigator

Lourdes P Dale, PhD
PRINCIPAL_INVESTIGATOR
University of Florida
John P Williamson, PhD
PRINCIPAL_INVESTIGATOR
University of Florida

Study Locations (Sites)

University of Florida McKnight Brain Institution
Gainesville, Florida, 32610
United States
UF Health Jacksonville
Jacksonville, Florida, 32209
United States

Collaborators and Investigators

Sponsor: University of Florida

  • Lourdes P Dale, PhD, PRINCIPAL_INVESTIGATOR, University of Florida
  • John P Williamson, PhD, PRINCIPAL_INVESTIGATOR, University of Florida

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-12-04
Study Completion Date2025-09-25

Study Record Updates

Study Start Date2024-12-04
Study Completion Date2025-09-25

Terms related to this study

Keywords Provided by Researchers

  • Polyvagal Theory
  • Adversity
  • Relaxation

Additional Relevant MeSH Terms

  • Music
  • Autonomic State