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Efficacy and safety of probiotics to improve sarcopenia in the elderly population

Evaluation of the efficacy and safety of probiotic supplementation to improve sarcopenic obesity in older adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094573
Enrollment
Unknown
Registered
2024-12-24
Start date
2024-12-30
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Elderly Sarcopenic Obesity

Interventions

Experimental group:24 weeks of probiotic supplement treatment
Control group:Placebo

Sponsors

The Affiliated Hospital of Hangzhou Normal University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 84 Years

Inclusion criteria

Inclusion criteria: 1.Between 60-84 years old, gender is not limited. 2.Obesity criteria: BMI >=28 kg/m^2 or waist circumference >=90cm for men and >=85cm for women. 3.Meet the criteria for sarcopenia: use the diagnostic criteria for sarcopenia recommended by the 2019 AWGS: a. Determine the limb skeletal muscle mass index (SMI) using a body composition analyzer, with male SMI <7.0kg/m^2 for men and <5.7kg/m^2 for women;b. Grip strength <28kg for men and <18kg for women;and c. 6m step speed <1.0m/s. The diagnosis of sarcopenia can be made if the criteria of a, b or c are satisfied. 4.No alcohol intake and no use of any probiotic-related foods or drugs, antibiotics, hormones, or weight loss products in the last 3 months.

Exclusion criteria

Exclusion criteria: 1.Secondary obesity, including cortisolism, hypothyroidism, insulinoma, drug-derived obesity, etc; 2. With severe osteoarthritis or neurological tissue lesions and other lesions that impede motor function; 3.With serious lesions such as serious heart, lung, kidney, brain lesions and other serious systemic or infectious diseases, such as malignant tumors, serious heart and lung diseases, neurological disorders, psychiatric disorders, HIV infection, schistosomiasis or hepatic schistosomiasis, epilepsy, and other viral mixed infections; 4.Inability to complete bioimpedance testing due to the setting of a pacemaker, etc; 5. Subjects who are unlikely to comply with the protocol at the judgment of the investigator, patients with severe physical or psychological illnesses that may affect effectiveness or safety; 6.Patients who are unable to cooperate in completing the entire intervention and follow-up due to various other factors.

Design outcomes

Primary

MeasureTime frame
Skeletal muscle index;

Secondary

MeasureTime frame
Indicators of glucose metabolism;Lipid metabolism indicators;Alteration intestinal flora;

Countries

China

Contacts

Public ContactLuo Yan

The Affiliated Hospital of Hangzhou Normal University

luoyanhz@163.com+86 158 6811 6339

Outcome results

None listed

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