NCT07513025 Effectiveness of RPT With Elastic Band in Tx of Sarcopenia in LTCFs
| NCT ID | NCT07513025 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Cishan Hospital, Ministry of Health and Welfare |
| Condition | Sarcopenia |
| Study Type | INTERVENTIONAL |
| Enrollment | 60 participants |
| Start Date | 2026-05-05 |
| Primary Completion | 2026-09-05 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 60 participants in total. It began in 2026-05-05 with a primary completion date of 2026-09-05.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The goal of this clinical trial is to evaluate the effectiveness of progressive resistance training using elastic bands in treating and delaying the progression of sarcopenia among older adults in long-term care facilities. Sarcopenia, characterized by a progressive decline in muscle mass and strength, affects more than 20% of individuals aged over 65 in Taiwan and is a significant risk factor for impaired daily functioning, falls, and increased mortality in older adults. While resistance or aerobic exercises are known to improve muscle strength and function in the elderly, such interventions are challenging to implement long-term in rural care facilities due to limited resources. The study aims to determine: Whether elastic band progressive resistance training can achieve clinical benefits in treating and delaying sarcopenia with minimal rehabilitation personnel. Whether this training model can be adapted to rural care facilities and other resource-limited settings, aligning with the goals of Taiwan's Long-Term Care 2.0 program. Participants will engage in a 12-week program, involving twice-weekly, 30-minute sessions of upper and lower limb resistance training using elastic bands. The training incorporates major muscle groups and proprioceptive neuromuscular facilitation (PNF) techniques. Primary outcomes: Skeletal muscle mass index of the limbs Dominant hand grip strength Walking speed SARC-F questionnaire scores Secondary outcomes: Maximal voluntary isometric contraction (MVIC) of the dominant hand Muscle thickness assessed via ultrasound Functional activities of the dominant upper limb Calf circumference Quality of life indicators The study will be conducted in long-term care facilities affiliated with or contracted by the Ministry of Health and Welfare Qishan Hospital. The findings aim to provide evidence for scalable, low-resource sarcopenia interventions suitable for rural and underserved populations.
Eligibility Criteria
Inclusion Criteria: 1. Older adults aged 60 years or above who are either receiving daycare services at long-term care facilities affiliated with or contracted by this hospital, or residents living in the hospital-affiliated nursing home. 2. Individuals with sufficient cognitive and physical capacity to participate in a progressive resistance training program incorporating elastic bands, with each session lasting at least 30 minutes. - Exclusion Criteria: 1. Inability to maintain a seated position for more than one hour. 2. Presence of uncontrolled hypertension, recent infections, major cardiovascular diseases, or other contraindications to exercise training as defined by the American College of Sports Medicine (ACSM). 3. Long-term bedridden individuals unable to participate in the progressive resistance training program incorporating elastic bands. 4. Individuals with respiratory diseases requiring regular oxygen support in daily life.
Contact & Investigator
Sheng-Hui Tuan, M.D.;Ph.D.
PRINCIPAL INVESTIGATOR
Cishan Hospital, Ministry of Health and Welfare, Kaohsiung, Taiwan
Frequently Asked Questions
Who can join the NCT07513025 clinical trial?
This trial is open to participants of all sexes, aged 60 Years or older, studying Sarcopenia. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07513025 currently recruiting?
Yes, NCT07513025 is actively recruiting participants. Contact the research team at pj73010@gmail.com for enrollment information.
Where is the NCT07513025 trial being conducted?
This trial is being conducted at Kaohsiung City, Taiwan.
Who is sponsoring the NCT07513025 clinical trial?
NCT07513025 is sponsored by Cishan Hospital, Ministry of Health and Welfare. The principal investigator is Sheng-Hui Tuan, M.D.;Ph.D. at Cishan Hospital, Ministry of Health and Welfare, Kaohsiung, Taiwan. The trial plans to enroll 60 participants.