CClinicalTrials.gg
CompletedNCT05462977REECOUpdated Nov 2, 2023

Rhythmically Entrained Exercise in Community-Dwelling Older Adults

An interventional study of Group exercise program in Exercise, Gait and Cognitive Decline, sponsored by University of North Carolina, Greensboro. Completed at 1 site in United States. Open to participants aged 55 Years to 99 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-11-02.

Sponsored by University of North Carolina, Greensboro · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
18
Allocation
Not applicable
Ages
55 Years to 99 Years
Sex
All
01

Study summary

Researchers at the University of North Carolina at Greensboro conduct a single-arm intervention trial to investigate the efficacy of a music-based group exercise program for community-dwelling older adults. Up to forty participants will be recruited to participate in a music-based light-to-moderate intensity group exercise program for 20 weeks (30 - 40 min/day, up to 6 days/week), which is designed for older adults with or without functional limitations to exercise with chairs for the improvement of aerobic capacity, upper and lower body strength, and balance control at a gradually increasing pace. During the exercise sessions, participants will be trained to move in time with music playlists in synchronous tempos. Primary outcomes are cognitive performance, mobility, and health-related quality of life measured before and after the intervention. Secondary outcomes are adherence to the exercise program as a potential mediator of the treatment.

Read the detailed description

Researchers at the University of North Carolina at Greensboro are conducting a single-arm intervention trial to investigate the efficacy of a music-based group exercise program for community-dwelling older adults. Up to forty participants will be recruited to participate in a music-based light-to-moderate intensity group exercise program for 20 weeks (30 - 40 min/day, up to 6 days/week), which is designed for older adults with or without functional limitations to exercise with chairs for the improvement of aerobic capacity, upper and lower body strength, and balance control at a gradually increasing pace. During the exercise sessions, participants will be trained to move in time with music playlists in synchronous tempos. Primary outcomes are cognitive performance, mobility, and health-related quality of life measured before and after the intervention. Secondary outcomes are adherence to the exercise program as a potential mediator of the treatment. The research team aims to determine whether (1) a music-based light-to-moderate intensity group exercise intervention beneficially impacts mobility, cognitive function, and health-related quality of life in community-dwelling older adults; (2) the treatment effect is mediated by adherence to physical activity; and (3) the treatment effect is moderated by cognitive impairment or functional limitations.

02

Conditions studied

  • Exercise
  • Gait
  • Cognitive Decline
  • Caregiver Burden
  • Cognitive Impairment
  • Dementia
  • Alzheimer Disease
  • Mild Cognitive Impairment
  • Respite Care
  • Mental Health
  • Depression
  • Music Therapy
  • Psychosocial Intervention
  • Cognition
  • Geriatric Assessment
  • Cognitive Dysfunction
  • Cognitive Aging
  • Outcome Assessment, Health Care
  • Balance
  • Fall
  • Walking
  • Affect
  • Physical Exertion
  • Memory Deficit
  • Memory Disorders
  • Memory Impairment
  • Neuropsychological Tests
  • Executive Function
  • Middle Aged
  • Healthy Aging
  • Elderly

Keywords

  • Physical Activity
  • Rhythmic Entrainment
  • Synchronous Music
  • Rhythmic Auditory Stimulation
  • Rhythmic Auditory Cue
  • Gait Training
  • Mobility
  • Movement
  • Perceived Exertion
  • Musical Pleasure
  • Groove
  • Memory
  • Executive Function
  • Older Adults
03

In context

Alzheimer Disease

3,678 studies on the registry are indexed under Alzheimer Disease; 872 are open to participants now.

This study's enrollment of 18 is below the median of 70 across 2,808 interventional studies indexed under Alzheimer Disease.

Browse Alzheimer Disease studies →

Lead sponsor

University of North Carolina, Greensboro is the lead sponsor of 20 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
55 Years to 99 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • 55 - 99 years old
  • Capable of being ambulatory with or without an assistive device.
  • No cardiac or pulmonary conditions or any neurological or musculoskeletal comorbidity or pain that would make light-intensity exercise dangerous, determined by the Physical Activity Readiness Questionnaire for Everyone or confirmed by their local medical practitioner if necessary.
  • Having adequate hearing for a conversation (including with hearing aids)
  • Capable of following the study procedures
  • No severe anxiety or depression
  • Mild to moderate cognitive impairment

Exclusion criteria

Exclusion Criteria:

  • Age younger than 55 or older than 99
  • Severe anxiety or depression
  • Severe cognitive impairment
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
18 participants (actual)

Study arms

  • Experimental
    Group exercise with beat-accented synchronous music stimulation

    Participants will be asked to participate in a music-based group exercise program for 24 weeks (up to 6 days/week, 30 - 45 min/day), which is designed for older adults with functional limitations to safely exercise on a chair or in a supported standing posture for the improvement of aerobic capacity, upper and lower body strength, and balance control at a gradually increasing pace based on the tempo of the beat-accented synchronous music playlists.

    Behavioral: Group exercise program

Interventions

  • BehavioralGroup exercise program

    Participants will be asked to join a music-based group exercise program for 24 weeks (up to 6 days/week, 30 - 45 min/day), which is designed for older adults with functional limitations to safely exercise on a chair or in a supported standing posture for the improvement of aerobic capacity, upper and lower body strength, and balance control at a gradually increasing pace in synchrony with music.

06

What researchers measure

Primary outcomes

  1. Change of fall risks

    Participants' fall risks will be measured by Timed Up \& Go Test

    Time frame: Baseline and change from baseline at month 5

  2. Change of walking endurance

    Participants' gait and walking endurance will be measured by 6-Minute Walk Test

    Time frame: Baseline and change from baseline at month 5

  3. Change of balance control

    Participants' balance control will be measured by 4-Stage Balance Test

    Time frame: Baseline and change from baseline at month 5

  4. Change of lower body strength

    Participants' lower body strength will be measured by 30-second Chair Stand Test

    Time frame: Baseline and change from baseline at month 5

  5. Change of cognitive function

    Participants' cognitive function will be measured through Montreal Cognitive Assessment , Flanker Inhibitory Control and Attention test, and Pattern Comparison Processing Speed Test.

    Time frame: Baseline and change from baseline at month 5

  6. Change of health-related quality of life

    EuroQol Health Questionnaire

    Time frame: Baseline and change from baseline at month 5

07

Study locations

1 site
  • UNC Greensboro
    Greensboro, North Carolina 27412, United States
08

References and documents

Publications

  • Park KS, Buseth L, Hong J, Etnier JL. Music-based multicomponent exercise training for community-dwelling older adults with mild-to-moderate cognitive decline: a feasibility study. Front Med (Lausanne). 2023 Aug 21;10:1224728. doi: 10.3389/fmed.2023.1224728. eCollection 2023. PubMed 37671396 ↗

Related links

Individual participant data

Plan to share: No — We don't have a plan to share IPD with other researchers at the moment.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 2, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05462977
Lead sponsor
University of North Carolina, Greensboro
Responsible party
Sponsor
First posted
Jul 18, 2022
Start date
May 1, 2022
Primary completion
Apr 28, 2023
Completion
Sep 30, 2023
Last update
Nov 2, 2023

Study contacts

Shin Park, PhD
principal investigator · University of North Carolina, Greensboro

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2023. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion