Music-Enhanced Calisthenics in Older Adults
Is Music-Enhanced Calisthenic Exercise More Effective in Healthy Sedentary Older Adults?
1 other identifier
interventional
31
1 country
1
Brief Summary
This study aimed to evaluate the effects of music-enhanced calisthenic exercises on balance, muscle strength, proprioception, and quality of life (QoL) in sedentary older adults. Thirty-one participants (mean age: 74.41 ± 5.86 years) were randomly assigned to three groups: Calisthenic Exercise Group (CEG), Music-based Calisthenic Exercise Group (MCEG), and Control Group (CG). The intervention consisted of 16 sessions over 8 weeks, including a 10-minute warm-up, 30 minutes of exercise, and a 10-minute cool-down. Assessments included the Timed Up and Go Test (balance), Sit-to-Stand Test (strength), joint position sense tests (proprioception), and the Nottingham Health Profile (QoL). Both exercise groups showed significant improvements in all measured outcomes (p\<0.05), with the MCEG demonstrating superior gains, particularly in energy levels and physical function. These findings support the use of music to enhance the benefits of exercise in older adults.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2024
1 active site
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 Start
First participant enrolled
January 2, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 2, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 2, 2025
CompletedFirst Submitted
Initial submission to the registry
May 7, 2025
CompletedFirst Posted
Study publicly available on registry
May 15, 2025
CompletedMay 15, 2025
May 1, 2025
1.1 years
May 7, 2025
May 7, 2025
Conditions
Outcome Measures
Primary Outcomes (4)
Balance Improvement
Change in balance as measured by the Timed Up and Go (TUG) Test. This test assesses functional mobility and balance, with a shorter completion time indicating better balance. Lower TUG scores at the end of the 8-week intervention indicate improved balance. Change in balance as measured by the Timed Up and Go (TUG) Test. This test assesses functional mobility and balance, with a shorter completion time indicating better balance. Lower TUG scores at the end of the 8-week intervention indicate improved balance.
Baseline and 8 weeks post-intervention
Muscle Strength Improvement
Change in lower limb muscle strength as measured by the Sit-to-Stand Test. This test counts the number of full stands a participant can perform in 30 seconds. Higher scores indicate better muscle strength.
Baseline and 8 weeks post-intervention
Proprioception Improvement
Change in joint position sense as measured by the Joint Position Sense Test. Smaller deviations from the target angle indicate better proprioceptive function.
Baseline and 8 weeks post-intervention
Quality of Life (QoL) Improvement Quality of Life (QoL) Improvement
Change in quality of life as measured by the Nottingham Health Profile (NHP), which assesses physical mobility, emotional reactions, social isolation, pain, and energy levels. Lower NHP scores indicate better perceived quality of life.
Baseline and 8 weeks post-intervention
Study Arms (3)
Arm 1: Music-based Calisthenic Exercise Group (MCEG)
EXPERIMENTALParticipants in this group will perform calisthenic exercises with background music for 8 weeks. Each session will include a 10-minute warm-up, 30 minutes of music-enhanced calisthenic exercises (e.g., seated leg lifts, chair squats, seated marching, arm curls, and seated torso twists), and a 10-minute cool-down. From the fifth week onwards, elastic resistance bands will be introduced to progressively increase exercise intensity. The music selection is designed to promote engagement and motivation, including rhythmic and motivational tracks suitable for older adults.
Arm 2: Calisthenic Exercise Group (CEG)
EXPERIMENTALParticipants in this group will perform the same calisthenic exercises as the MCEG but without background music. The intervention will last 8 weeks, with each session including a 10-minute warm-up, 30 minutes of calisthenic exercises (e.g., seated leg lifts, chair squats, seated marching, arm curls, and seated torso twists), and a 10-minute cool-down. From the fifth week onwards, elastic resistance bands will be introduced to progressively increase exercise intensity.
Arm 3: Control Group (CG)
NO INTERVENTIONParticipants in this group will not receive any structured exercise intervention during the 8-week study period. They will be encouraged to maintain their usual daily activities without any specific exercise regimen. This group serves as a baseline for comparison against the exercise groups.
Interventions
Participants in this group will perform 8 weeks of calisthenic exercises with background music. Each session includes a 10-minute warm-up, 30 minutes of music-based exercises (e.g., seated leg lifts, chair squats, arm curls), and a 10-minute cool-down. Elastic resistance bands will be introduced from week 5 to increase intensity. Music tracks are selected to enhance motivation and engagement.
Eligibility Criteria
You may qualify if:
- Only individuals deemed physically suitable for exercise by the institutional physician and who agreed to participate in the exercise program were included.
You may not qualify if:
- Individuals under 65 years of age.
- Severe cognitive impairment or diagnosed dementia that would prevent safe participation in the exercise program.
- Severe musculoskeletal, neurological, or cardiovascular conditions that contraindicate physical exercise.
- Acute or unstable medical conditions requiring immediate medical intervention.
- Hearing impairment that would significantly reduce the ability to follow music-based exercises.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Niğde Ömer Halisdemir University, Faculty of Health Sciences
Niğde, Ni̇ğde, 51700, Turkey (Türkiye)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
May 7, 2025
First Posted
May 15, 2025
Study Start
January 2, 2024
Primary Completion
February 2, 2025
Study Completion
April 2, 2025
Last Updated
May 15, 2025
Record last verified: 2025-05
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF
- Time Frame
- Baseline (Pre-intervention) and 8 weeks post-intervention
Anonymized individual participant data, including demographic information, Timed Up and Go (TUG) test scores, Sit-to-Stand test results, joint position sense measurements, and Nottingham Health Profile (NHP) scores, will be made available upon reasonable request. Data will be shared through a secure institutional repository following publication of the primary manuscript. Access will be granted to qualified researchers for the purpose of validating findings or conducting further analysis, in accordance with ethical guidelines.