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Electroacupuncture for Sarcopenia in the Elderly: A Randomized Controlled Trial

Electroacupuncture for Sarcopenia in the Elderly: A Randomized Controlled Trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300079294
Enrollment
Unknown
Registered
2023-12-29
Start date
2023-12-29
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Sarcopenia

Interventions

Electroacupuncture Group:Electroacupuncture
Placebo Electroacupuncture Group:Sham Electroacupuncture

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Meets the diagnostic criteria for "sarcopenia" as outlined in the "2019 Asian Sarcopenia Diagnosis Consensus" published by the Asian Working Group for Sarcopenia; 2) Age between 60 and 80 years old, no gender restrictions; 3) Signs the informed consent form and voluntarily participates in this trial.

Exclusion criteria

Exclusion criteria: 1) Have a background as a professional or semi-professional athlete. 2) Suffer from underlying medical conditions that may lead to malnutrition, such as heart failure, chronic obstructive pulmonary disease (COPD), chronic kidney failure, anorexia, etc. These conditions can result in appetite loss and indigestion among the elderly population. Additionally, mental disorders and cognitive impairment can also contribute to decreased food intake in older individuals. 3) Have underlying diseases that cause muscle wasting, including malignant tumors, neuromuscular disorders, and fractures that have not healed within a three-month period. 4) Experience physical disability or injury to the upper or lower limbs within the past three months which may impact grip strength measurement or walking speed assessment. 5) Take medications known to significantly affect musculoskeletal function. 6) Possess implanted electronic devices or orthopedic metal implants within the body. 7) Struggle with drug or alcohol dependence/abuse issues. 8) Currently enrolled in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Patient's grip strength change after 8-week treatment;

Secondary

MeasureTime frame
Patient's grip strength change rate at week 4 and week 20 ;Skeletal Muscle Index (SMI) change rate;The Short Physical Performance Battery (SPPB);IPAQ (Daily functional evaluation);Subjective Assessment of Treatment Efficacy by Patients;Serum CRP, IL-6, and TNF-a levels;SF-12 (quality of life );

Countries

China

Contacts

Public ContactLingyun Lu

West China Hospital, Sichuan University

lingyun.lu@scu.edu.cn+86 185 8395 5132

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026