NCT07338500

Brief Summary

The purpose of this study is to examine how listening to music compares to guided mindfulness in affecting blood pressure, heart rate, and feelings of anxiety in healthy adults. The investigators aim to determine whether one of these approaches is more effective in reducing these variables. Additionally, the study will explore whether personal traits or preferences, measured using questionnaires, influence how participants respond to music or mindfulness. Based on previous clinical findings, the researchers hypothesize that listening to music will lead to greater reductions in blood pressure and heart rate compared to guided mindfulness.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
3mo left

Started Apr 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress25%
Apr 2026Aug 2026

First Submitted

Initial submission to the registry

December 12, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

January 14, 2026

Completed
3 months until next milestone

Study Start

First participant enrolled

April 10, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2026

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Last Updated

April 24, 2026

Status Verified

April 1, 2026

Enrollment Period

2 months

First QC Date

December 12, 2025

Last Update Submit

April 21, 2026

Conditions

Keywords

MusicMindfulness

Outcome Measures

Primary Outcomes (2)

  • Changes in Blood Pressure

    The investigators will compare changes in systolic and diastolic blood pressure between the curated music playlist and guided mindfulness interventions using an automated oscillometric upper arm blood pressure monitor with measurements taken at 10-minute intervals.

    0, 10, 20, 30, and 40 minutes during each 40-minute intervention session.

  • Changes in Heart Rate

    The investigators will compare changes in heart rate between the curated music playlist and guided mindfulness interventions using an automated oscillometric upper arm blood pressure monitor with measurements taken at 10-minute intervals.

    0, 10, 20, 30, and 40 minutes during each 40-minute intervention session.

Secondary Outcomes (9)

  • Changes in Beat-to-Beat Blood Pressure (Finapres NOVA)

    0 to 40 minutes during each 40-minute intervention session.

  • Changes in Heart Rate (Finapres NOVA, Electrocardiogram-derived)

    0 to 40 minutes during each 40-minute intervention session.

  • Change from Baseline in STAI-Y 1

    Baseline and immediately after each of the two 40-minute intervention sessions during the single study visit.

  • Change from Baseline in Edmonton Symptom Assessment System (ESAS)

    Baseline and immediately after each of the two 40-minute intervention sessions during the single study visit.

  • Barcelona Music Reward Questionnaire (BMRQ)

    Baseline

  • +4 more secondary outcomes

Study Arms (2)

Music Intervention First

EXPERIMENTAL

Participants randomized to this arm will receive a 40-minute Music Listening intervention in the first period, followed by a 20-minute washout period, and then receive a 40-minute Guided Mindfulness intervention in the second period.

Other: MusicOther: Mindfulness

Mindfulness Intervention First

EXPERIMENTAL

Participants randomized to this arm will receive a 40-minute Guided Mindfulness intervention in the first period, followed by a 20-minute washout period, and then receive a 40-minute Music Listening intervention in the second period.

Other: MusicOther: Mindfulness

Interventions

MusicOTHER

Participants will listen to a 40-minute playlist, curated by the research team, through noise-cancelling headphones. The playlist will simultaneously be played in the room through speakers.

Mindfulness Intervention FirstMusic Intervention First

Participants will engage in a structured mindfulness session led by a member of the research team with experience in mindfulness-based practices.

Mindfulness Intervention FirstMusic Intervention First

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Normal baseline blood pressure (systolic BP \< 120 mmHg and diastolic BP \< 80mmHg).
  • Abstention from caffeine intake for at least 12 hours before the study session and throughout the session, as caffeine may influence cardiovascular measurements.
  • Abstention from using nicotine or tobacco products for at least 1 hour before the study session and throughout the session, as these substances may influence cardiovascular measurements.

You may not qualify if:

  • Significant hearing impairments that cannot be improved with hearing aids or sound amplification.
  • Current use of medications that could affect blood pressure.
  • History of hypertension or cardiovascular disease.
  • Diagnosis of active substance use disorder, or reported patterns of alcohol, cannabis, or recreational/non-prescribed substance use likely to affect cardiovascular function.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Jewish General Hospital

Montreal, Quebec, H3T 1E2, Canada

RECRUITING

MeSH Terms

Interventions

Music TherapyMindfulness

Intervention Hierarchy (Ancestors)

Sensory Art TherapiesComplementary TherapiesTherapeuticsRehabilitationAftercareContinuity of Patient CarePatient CarePsychotherapyBehavioral Disciplines and ActivitiesCognitive Behavioral TherapyBehavior Therapy

Study Officials

  • Kyle Greenway, MD

    Sir Mortimer B. Davis - Jewish General Hospital, McGill University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Elizabeth Misener, BSc

CONTACT

Sara de la Salle, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Psychiatrist

Study Record Dates

First Submitted

December 12, 2025

First Posted

January 14, 2026

Study Start

April 10, 2026

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

August 1, 2026

Last Updated

April 24, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Due to the sensitive nature of the data and the small sample size, which poses a risk of participant identification, the data will not be shared.

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