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Validation and Effect Evaluation of Exercise Intervention Program for Elderly Patients with Sarcopenia Based on the Complex Intervention Framework

Validation and Effect Evaluation of Exercise Intervention Program for Elderly Patients with Sarcopenia Based on the Complex Intervention Framework

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117942
Enrollment
Unknown
Registered
2026-01-30
Start date
2025-09-03
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

Sarcopenia

Interventions

Experimental group:excercise intervention
Control group:Routine care for sarcopenia

Sponsors

Guangdong Provincial Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients: (1) Age 60–85 years; (2) Meet the diagnostic criteria for sarcopenia as established by the Asian Working Group for Sarcopenia in 2019; (3) Conscious, vital signs stable, able to communicate normally; (4) Able to independently complete measurements such as walking speed and grip strength; (5) Signed the informed consent form and voluntarily participate in this study. 2. Patients' family members: (1) Family members of patients in the trial group. (2) Voluntarily participate in interviews and sign the informed consent form. (3) Conscious and able to clearly express their own thoughts and experiences. 3. Medical personnel: (1) Hold relevant professional qualification certificates and participate in exercise interventions for elderly patients with sarcopenia; (2) Educational background: doctors with a master's degree or above; nurses with a college degree or above; (3) Work experience: registered medical personnel with more than five years of clinical experience; (4) Voluntarily participate in interviews and sign the informed consent form. (5) Conscious and able to clearly express their own thoughts and experiences.

Exclusion criteria

Exclusion criteria: 1. Patients: (1) Patients with critical or severe heart failure, liver dysfunction, end-stage renal dialysis, malignant tumors, or neuromuscular transmission disorders; (2) Patients with mental illness or intellectual disabilities; (3) Patients with implanted cardiac pacemakers; (4) Patients with recent surgery or other conditions preventing normal physical activity, such as those who have had knee or hip surgery; (5) Patients who have participated in supervised systematic exercise in the past three months; or have undergone hormone or immunosuppressive therapy within the past 6 months. 2. Patients' family members: (1) Those with communication difficulties; (2) Those who withdraw from the interview midway. 3. Medical staff: (1) Medical staff who are on external rotations, further training, or absent due to marital leave, maternity leave, etc.; (2) Doctors or nurses currently undergoing standardized training and/or further studies; (3) Those who do not consent to audio recording; (4) Those who withdraw from the interview midway.

Design outcomes

Primary

MeasureTime frame
grip strength;feasibility;

Secondary

MeasureTime frame
safety;appendicular skeletal muscle index;6m walking speed;acceptability;effectiveness;patient exercise intention;Observability of Intervention;5 times sit up tests;calf circumference;

Countries

China

Contacts

Public ContactWei Lin

Guangdong Provincial Hospital of Traditional Chinese Medicine

Weilin22@126.com+86 20 81887233

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026