The Effectiveness of Squat Exercise for Improving Pre-Sarcopenia in Order Adults
2 other identifiers
interventional
80
1 country
1
Brief Summary
With the growing aging population, it has been reported that approximately 10-20% of older adults have pre-sarcopenia. Pre-sarcopenia is defined as a decline in either muscle mass or muscle strength. Previous studies have indicated that squat exercise has significant effects on improving lower-extremity muscle strength and physical performance. Early intervention through resistance exercise during the pre-sarcopenia stage may increase muscle mass, enhance physical performance, and prevent progression to sarcopenia. Therefore, the purpose of this study is to investigate the effects of squat exercise on improving pre-sarcopenia among older adults. It is expected that, following the squat exercise intervention, older adults will demonstrate significant improvements in muscle mass, lower-extremity muscle strength, physical performance, and body composition, thereby alleviating pre-sarcopenia.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2026
Typical duration 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
March 6, 2026
CompletedFirst Submitted
Initial submission to the registry
June 27, 2026
CompletedFirst Posted
Study publicly available on registry
July 24, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2028
July 24, 2026
July 1, 2026
10 months
June 27, 2026
July 21, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Physical performance assessed by the Short Physical Performance Battery (SPPB)
Physical performance will be assessed using the Short Physical Performance Battery (SPPB). The SPPB consists of three components: balance test, gait speed test, and chair stand test. Total scores range from 0 to 12 points, with higher scores indicating better physical performance
Baseline, 6 weeks, and 12 weeks
Body composition assessed by bioelectrical impedance analysis (InBody)
Body composition will be assessed using bioelectrical impedance analysis (InBody).Measurements include skeletal muscle mass, body fat mass, and body fat percentage.
Baseline, 6 weeks, and 12 weeks
Study Arms (2)
Squat Exercise
EXPERIMENTALThe researcher first assists participants in completing the questionnaire and measures older adults' InBody composition, grip strength, and SPPB (Short Physical Performance Battery). A 12-week squat exercise intervention is then implemented. Post-intervention assessments are conducted at Week 6 and Week 12.
Intervention: Usual Care
NO INTERVENTIONNo specific resistance training is performed, and participants maintain their usual daily activities.
Interventions
Squat exercise is an effective resistance training intervention that enhances lower-extremity muscle strength, physical performance, and functional ability, thereby helping prevent or delay sarcopenia in older adults.
Eligibility Criteria
You may qualify if:
- Older adults aged 65 years and above who meet at least one criterion of pre-sarcopenia.
- Residents of Hualien.
- Able to read, have clear consciousness, and communicate in Mandarin.
- Willing to participate in this study.
You may not qualify if:
- Individuals with disability.
- Individuals with psychiatric disorders or other conditions affecting cognitive function.
- Individuals with injuries of the knee, hip, or lumbar spine that prevent participation in squat exercise.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hsiao-Chien,Tseng
Taipei, Taiwan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
HSIAO-CHIEN TSENG, MASTER
STUDENT
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- PREVENTION
- Intervention Model
- SEQUENTIAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
June 27, 2026
First Posted
July 24, 2026
Study Start
March 6, 2026
Primary Completion (Estimated)
December 31, 2026
Study Completion (Estimated)
December 31, 2028
Last Updated
July 24, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share