Actively Recruiting

Phase Not Applicable
Age: 18Years - 89Years
All Genders
Healthy Volunteers
NCT06710886

Listening to Calming Music

Led by University of Florida · Updated on 2026-03-10

100

Participants Needed

2

Research Sites

107 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Listening to Calming Music

Who Can Participate

Age: 18Years - 89Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Between the ages of 18 and 89 (Phase 1)
  • Proficient in English
  • Attendees of an online workshop session (Phase 1)
  • Between the ages of 18 and 45 (Phase 2)
  • Proficient in English (Phase 2)
Not Eligible

You will not qualify if you...

  • Over the age of 89 (Phase 1)
  • Over the age of 45 (Phase 2)

AI-Screening

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Trial Site Locations

Total: 2 locations

1

University of Florida McKnight Brain Institution

Gainesville, Florida, United States, 32610

Actively Recruiting

2

UF Health Jacksonville

Jacksonville, Florida, United States, 32209

Completed

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Research Team

L

Lourdes P Dale, PhD

CONTACT

A

Audrey N Dana

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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