- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07581639
Comparison of Live and Virtual Music-based Interventions in Mitigating Stress
May 12, 2026 updated by: University of Pennsylvania
Comparison of Live and Virtual Music-based Interventions in Mitigating Stress: A Pilot Study
The purpose of this study is to learn if virtual music therapy with active engagement components leads to the same benefits as traditional live music therapy in mitigating stress in older adults.
This study aims to compare live and virtual music interventions among older adults with cognitive impairment living in assisted living facilities.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
32
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Pennsylvania
-
Berwyn, Pennsylvania, United States, 19312
- Conestoga High School
-
-
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.
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Lives in included assisted living facility
- 65 years or older
- Able to provide informed consent
- Able to hear music
- Able to see a computer screen
- Able to speak
Exclusion Criteria:
- Does not live in included assisted living facility
- Younger than 65 years
- Unable to provide informed consent
- Unable to hear music
- Unable to see a computer screen
- Unable to speak
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Live music therapy
The live music intervention was presented in the activities room of each senior center and included a classical violin for the performer (a classically trained violinist with experience arranging and playing pop music), a second violin for participant engagement, and a computer speaker for digital sound output (Dell, Inc.).
The live music intervention sessions included multiple active engagement components, such as music adjustment (e.g., lowering the tempo, changing to an upbeat piece) to match participants' apparent mood, verbal interaction, physical engagement (e.g., encouraging dancing, on-beat clapping), and singing along.
|
The live music intervention was presented in the activities room of each senior center and included a classical violin for the performer (a classically trained violinist with experience arranging and playing pop music), a second violin for participant engagement, and a computer speaker for digital sound output (Dell, Inc.).
The live music intervention sessions included multiple active engagement components, such as music adjustment (e.g., lowering the tempo, changing to an upbeat piece) to match participants' apparent mood, verbal interaction, physical engagement (e.g., encouraging dancing, on-beat clapping), and singing along.
|
|
Experimental: Virtual music therapy
The virtual intervention followed identical procedures as the live intervention and involved similar active engagement components, with the music being delivered to the same cohort via video conference (Zoom Communications, Inc.).
|
The virtual intervention followed identical procedures as the live intervention and involved similar active engagement components, with the music being delivered to the same cohort via video conference (Zoom Communications, Inc.).
In both live and virtual sessions, the performer showed identical levels of engagement and adjustment.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Heart rate (HR)
Time Frame: Baseline (15 minutes before the music intervention session) and follow-up (15 minutes after the music intervention session was completed)
|
Registered nurses at each assisted living facility measured and recorded each participant's heart rate (HR) using an oxygen saturation monitor (Oxiline, Inc.).
The monitor was placed on each participants' finger and the heart rate was recorded for a 1-minute interval 15 minutes before and after each music-based session.
|
Baseline (15 minutes before the music intervention session) and follow-up (15 minutes after the music intervention session was completed)
|
|
Systolic blood pressure
Time Frame: Baseline (15 minutes before the music intervention session) and follow-up (15 minutes after the music intervention session was completed)
|
Systolic blood pressure was measured using a sphygmomanometer (Curaplex, Inc.) immediately after the heart rate measurement
|
Baseline (15 minutes before the music intervention session) and follow-up (15 minutes after the music intervention session was completed)
|
|
Self-reported stress levels
Time Frame: Baseline (15 minutes before the music intervention session) and follow-up (15 minutes after the music intervention session was completed)
|
The self-reported stress survey was adapted and modified from Levenstein et al. (1993), with question wording modified to reduce the reading level.
The stress-assessment survey was condensed to a total of 10 questions, each rated on a 4-level Likert scale from strongly disagree (0) to strongly agree (3).
To maintain consistency, the rating on 4 items indicating lack of stress was reversed, so that 0 corresponded to 3 points.
The total score was calculated by adding the individual scores for each question (score range, 0 to 30, where a higher rating corresponds to greater stress).
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Baseline (15 minutes before the music intervention session) and follow-up (15 minutes after the music intervention session was completed)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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 Major Dates
Study Start (Actual)
August 1, 2025
Primary Completion (Actual)
September 27, 2025
Study Completion (Actual)
September 27, 2025
Study Registration Dates
First Submitted
April 27, 2026
First Submitted That Met QC Criteria
May 5, 2026
First Posted (Actual)
May 12, 2026
Study Record Updates
Last Update Posted (Actual)
May 15, 2026
Last Update Submitted That Met QC Criteria
May 12, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 01082025
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Informed consent to share individual participant data was not obtained.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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