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Prevalence and Risk Factor Analysis of Sarcopenia in a High-Risk Osteoporosis Population

Prevalence and Risk Factor Analysis of Sarcopenia in a High-Risk Population for Osteoporosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129483
Enrollment
Unknown
Registered
2026-08-05
Start date
2025-11-12
Completion date
Unknown
Last updated
2026-08-10

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

Conditions

Osteoporosis

Interventions

Osteoporosis High-Risk Population Observation Group:None

Sponsors

The Second Affiliated Hospital of the Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 99 years, male or female; 2. Individuals at high risk of osteoporosis, as defined by the Guidelines for the Diagnosis and Treatment of Primary Osteoporosis (2022), meeting any one of the following criteria (see Appendix 1): (1) Positive IOF 1-minute test; (2) OSTA index < -1; (3) Other risk factors for osteoporosis, such as patients with moderate-to-high fracture risk assessed by FRAX®; 3. Voluntarily participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Individuals with acute exacerbation or decompensated phase of various chronic diseases (including heart, lung, liver, and kidney diseases) who, in the investigator's judgment, are unable to safely complete physical function tests; 2. Those who have experienced a fracture or undergone orthopedic surgery within the past 3 months; 3. Individuals with concurrent malignant tumors (life expectancy 7.5 mg/day for > 3 months) or other potent medications affecting muscle/bone metabolism; 5. Those with cognitive impairment, mental illness, or communication disorders that prevent understanding of the study content or cooperation with the assessment; 6. Individuals with limited mobility due to neurological diseases (e.g., hemiplegia, Parkinson's disease), severe osteoarthritis, or diabetic foot, rendering them unable to independently complete the 6-meter walk or sit-to-stand test; 7. Any other conditions that, in the opinion of the investigator, make the individual unsuitable for participation in this study.

Design outcomes

Secondary

MeasureTime frame
muscle mass (ASMI measured by DXA), handgrip strength, and physical function (gait speed, 5-time chair stand test, SPPB);handgrip strength; physical function (gait speed, 5-time chair stand test, SPPB);

Primary

MeasureTime frame
The prevalence of sarcopenia;

Countries

China

Contacts

Public ContactQixian Wang

The Second Affiliated Hospital of the Army Medical University

527272680@qq.com+86 23 6877 4625

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026