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Recruiting Not applicable

A Home-based Multicomponent Exercise Intervention Program Based on the Fogg Behavior Model (FBM) for Older Adults With Osteosarcopenia and Frailty

NCT07845656 · tracked via the Priya Life Science China tracker
Phase
Not applicable
Started
2026-01-01
Last updated
2026-09-29

Condition(s) studied

Osteosarcopenia; Frailty; Older Adults

Investigational drug(s) / intervention(s)

Multi-component home-based exercise intervention based on the Fogg Behavior Modelroutine health education and standard nursing care for osteoporosis and regular outpatient follow-up, without extra exercise and nutritional intervention.

Multi-component home-based exercise intervention based on the Fogg Behavior Model: Participants receive a 6-month multi-component home-based exercise intervention based on the Fogg Behavior Model, divided into 3 stages. Stage 1 (Weeks 1-2): motivation cultivation, health assessment, risk screening and health education. Stage 2 (Weeks 3-12): personalized exercise prescription including warm-up, aerobic, resistance, balance and flexibility training, with progressive intensity and regular follow-up. Stage 3 (Months 4-6): habit formation, self-management reinforcement and incentive strategies. The intervention aims to improve muscle mass, physical function and frailty status in older adults with sarcopenia-osteoporosis.

routine health education and standard nursing care for osteoporosis and regular outpatient follow-up, without extra exercise and nutritional intervention.: Participants receive routine osteoporosis health education and standard nursing care. General advice on diet, fall prevention and daily activity is provided, without the multi-component staged exercise intervention based on the Fogg Behavior Model. Regular outpatient follow-up is arranged.

Study summary

This study aims to construct and evaluate a home-based multicomponent exercise intervention program based on the Fogg Behavior Model for older adults with osteosarcopenia and frailty. Eligible participants will be randomly divided into two groups. The intervention group will receive the home multicomponent exercise guidance built on Fogg Behavior Model, while the control group will get routine health education. We will compare frailty status, muscle strength, physical function,bone mineral density and quality of life between the two groups at baseline, 3 months and 6 months, to explore whether this intervention can improve physical function and reduce frailty in elderly patients with osteosarcopenia.

Eligibility

Sex
ALL
Min age
60 Years
Max age
85 Years
Healthy volunteers
No
Inclusion Criteria: 1. The disease is in stable condition. 2. Aged 60-85 years or older. 3. Meet the diagnostic criteria in the 2022 Expert Consensus on Sarcopenia-Osteoporosis. 4. The score of frailty scale is ≥1, indicating patients are in pre-frailty or frailty status. 5. Clear consciousness, normal communication, capable of cooperating with exercise intervention; not living alone and will not leave the residence within half a year. 6. Own a smartphone and voluntarily participate in this study. Exclusion Criteria: 1. Severe cardiopulmonary, hepatic or renal dysfunction. 2. Uncontrolled severe neurological or psychiatric diseases. 3. Recent fracture or unable to perform exercise training. 4. Malignant tumor, severe infectious disease. 5. Participate in other exercise intervention studies simultaneously. 6. Cognitive impairment and cannot cooperate with follow-up.

Primary outcome measure(s)

  • Change in frailty phenotype score at 6 months — Baseline, 3 months, 6 months
    The change of Fried frailty phenotype score from baseline to 6-month follow-up. Fried frailty scale ranges from 0 to 5, higher score means worse frailty status.

Trial sites (2)

FacilityCityRegionStatus
Nantong First People's Hospital Nantong Jiangsu Recruiting
Nantong First People's Hospital Nantong Jiangsu Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07845656 on ClinicalTrials.gov ↗ ← All trials in China