Exercise Snacks for Muscle Strength in Older Adults With Possible Sarcopenia
Effects of Exercise Snacks Versus Home-Based Resistance Training on Muscle Strength in Older Adults With Possible Sarcopenia: A Randomized Controlled Trial
1 other identifier
interventional
60
1 country
1
Brief Summary
This study aims to investigate whether exercise snacks, a time-efficient approach involving short bouts of exercise performed throughout the day, can improve muscle strength in older adults with possible sarcopenia. Participants will be randomly assigned to an exercise snacks group, a home-based resistance training group, or a non-exercise control group. The intervention will last 8 weeks. Muscle strength and physical function will be assessed before and after the intervention.
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 May 2026
Shorter than P25 for not_applicable
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
May 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 25, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
July 25, 2026
CompletedFirst Submitted
Initial submission to the registry
September 10, 2026
CompletedFirst Posted
Study publicly available on registry
September 15, 2026
CompletedSeptember 15, 2026
September 1, 2026
2 months
September 10, 2026
September 10, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Handgrip Strength
Handgrip strength was assessed using a hydraulic dynamometer. Participants performed three maximal voluntary contractions with the dominant hand, and the highest peak force was used for analysis.
Baseline and after 8 weeks of intervention
Secondary Outcomes (4)
Five-Time Chair Stand Test
Baseline and after 8 weeks of intervention
30-Second Chair Stand Test
Baseline and after 8 weeks of intervention
Isokinetic Knee Peak Torque
Baseline and after 8 weeks of intervention
Exercise Adherence
During the 8-week intervention
Study Arms (3)
Exercise Snacks Group
EXPERIMENTALParticipants completed an 8-week exercise snacks intervention consisting of brief exercise sessions distributed throughout the day. The exercise protocol included sit-to-stand, alternating seated knee extension, alternating standing knee flexion, high-knee marching in place, and wall push exercises.
Home-based Resistance Training Group
ACTIVE COMPARATORParticipants completed an 8-week structured home-based resistance training program using the same bodyweight exercise protocol as the exercise snacks group but with a different exercise schedule.
No Intervention
NO INTERVENTIONParticipants maintained their habitual lifestyle during the 8-week intervention period and did not receive any structured exercise program.
Interventions
The exercise snacks intervention consisted of brief bouts of bodyweight exercises performed throughout the day for 8 weeks. Participants completed three exercise sessions per day, five days per week. Each session included five exercises: sit-to-stand, alternating seated knee extension, alternating standing knee flexion, high-knee marching in place, and wall push.
Participants completed an 8-week home-based resistance training program using the same bodyweight exercises as the exercise snacks group. Training was performed three days per week with multiple exercise sessions completed on each training day.
Eligibility Criteria
You may qualify if:
- Community-dwelling older adults aged 60 years or older.
- Meeting the criteria for possible sarcopenia according to the Asian Working Group for Sarcopenia (AWGS) 2019 consensus.
- Handgrip strength less than 28 kg for men or less than 18 kg for women.
- Five-time chair stand test time of 12 seconds or longer.
- Able to independently complete the exercise protocol and outcome assessments.
- Provided written informed consent before participation.
You may not qualify if:
- Presence of contraindications to physical activity according to the Physical Activity Readiness Questionnaire (PAR-Q).
- Participation in regular structured resistance training.
- Use of medications or treatments likely to substantially affect muscle strength.
- Participation in other interventional studies within the previous three months.
- Unable to complete the five-time chair stand test independently.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Ziren Zhaolead
Study Sites (1)
Sports Centre
Chongqing, Chongqing Municipality, China
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
September 10, 2026
First Posted
September 15, 2026
Study Start
May 13, 2026
Primary Completion
July 25, 2026
Study Completion
July 25, 2026
Last Updated
September 15, 2026
Record last verified: 2026-09