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Effect of vibration training vs. conventional resistance training on sarcopenia among community-dwelling older people with sarcopenia: 3-arm randomized controlled trial protocol

Effect of vibration training vs. conventional resistance training on sarcopenia among community-dwelling older people with sarcopenia: 3-arm randomized controlled trial protocol

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051178
Enrollment
Unknown
Registered
2021-09-15
Start date
2021-09-15
Completion date
Unknown
Last updated
2022-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sarcopenia

Interventions

Vibration trainign group:a 30-min three weekly whole-body vibration training (WBVT) with the frequency of 40 Hz and peak-to-peak amplitude of 4 mm
Resistance training group:60%-70% 1RM resistance training

Sponsors

Chongming branch of Xinhua Hospital Affiliated to Medical College of Shanghai Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Aged >=65 years; 2.Older people are diagnosed as sarcopenia according to the criteria for AWGS: appendicular skeletal muscle mass index (ASMI) < 7 kg/m2 for male (M) and <5.7 kg/m2 for female (F), using bioelectrical impedance analyzer (BIA); handgrip strength (HGS), M: < 28 kg, F: <18 kg; and/or gait speed (GS) <1 m/s by 6-meter walk test (6MWT); 3.The participants without following serious diseases, such as uncontrolled hypertension, hyperlipidemia, hyperglycemia, and diabetes; 4.The participants without following untreated diseases, such as gallstones or kidney stones, and infectious diseases; 5.The participants have no regular exercise habit for more than 3 months.

Exclusion criteria

Exclusion criteria: 1.The participants have absolute contraindication for exercising, such as deep venous thrombosis and/or blood clotting disorders; 2.The participants have serious cognitive impairments that effect the assessments and communication by researchers, such as dementia, mental illness 3.The participants suffered from serious diseases affect the assessments and interventions, such as musculoskeletal diseases (such as fracture, dislocation, osteoporosis, rheumatoid arthritis) and disability (such as loss of hands, feet or limbs); 4.The participants have serious spinal diseases or surgical history, such as vertebral fracture, inflammatory joint disease, ankylosing spondylitis, spondylolisthesis, rheumatism, cauda equina syndrome, tumor; 5.The participants have the history of following cardiovascular diseases, such as stroke, heart failure, coronary heart disease, epilepsy; 6.The participants who have taken the following drugs regularly in recent 3 months: antiplatelet agents (such as aspirin, aggrenox, cilostazol, eptifibatide, ticlopidine, and tirofiban), anticoagulant drug and analgesic drugs; 7.The participants have other diseases, which is judged by the professional doctors that participation in this study is not recommended; 8.The participants who dont sign the informed consent before the beginning of experiment.

Design outcomes

Primary

MeasureTime frame
Lower limb muscle strength;

Secondary

MeasureTime frame
Anthropometric Measurements;Muscle mass;Handgrip strength;Physical performance;quality of life;

Countries

China

Contacts

Public ContactChen Nan

Chongming branch of Xinhua Hospital Affiliated to Medical College of Shanghai Jiaotong University

chennanreha@126.com+86 18101843311

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026