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Construction and Application of a Daily-Life Scenario-Based Exercise Training Intervention Program for Community-Dwelling Older Adults with Presarcopenia

Construction and Application of a Daily-Life Scenario-Based Exercise Training Intervention Program for Community-Dwelling Older Adults with Presarcopenia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111292
Enrollment
Unknown
Registered
2025-10-29
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

Presarcopenia

Interventions

Control group:The control group maintains their previous daily activities and lifestyle, and receives routine community health education, including: 1. Exercise guidance: Informing older adults abou
2. Dietary guidance: Advising older adults on principles of balanced nutrition to improve nutrient intake
3. Education on disease-related knowledge, etc.
Trial group:The experimental group implements the scenario-based exercise training program. Based on the Information Motivation Behavioral Skills Model as the theoretical framework, the program compri
motivational intervention consists of motivational interviewing
behavioral skills intervention delivers scenario-based exercise training and assists community-dwelling older adults in completing the training.

Sponsors

North China University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Meets the diagnostic criteria for pre-sarcopenia in the *Chinese Guidelines for Sarcopenia Diagnosis and Treatment (2024 Edition)*, characterized by low muscle strength only (males =7.0 kg/m^2, females muscle mass >=5.7 kg/m^2); 2. Age >=60 years; 3. Residing in the community for at least 6 months; 4. Provided informed consent and voluntarily participates in this study.

Exclusion criteria

Exclusion criteria: 1. Those with severe cardiac, cerebral, or other organ dysfunction, or in the acute phase of a disease, for whom training is impaired; 2. Those with cognitive impairment who are unable to communicate normally; 3. Those who are participating in other projects during the study period.

Design outcomes

Primary

MeasureTime frame
Grip Strength;Muscle Mass;

Secondary

MeasureTime frame
Calf Circumference;6-Meter Walk Test;5-Time Chair Stand Test;Berg Balance Scale;Self-efficacy for Exercise Scale;Brief Illness Perception Questionnaire;

Countries

China

Contacts

Public ContactTang Zhenghao

North China University of Science and Technology

1105724391@qq.com+86 137 3150 9123

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026