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Recruiting NCT06547593

A Multifaceted Nutrition Intervention for Frailty in the Community Elderly

Trial Parameters

Condition Frail
Sponsor Zhaofeng Zhang
Study Type INTERVENTIONAL
Phase N/A
Enrollment 315
Sex ALL
Min Age 65 Years
Max Age 85 Years
Start Date 2024-07-30
Completion 2025-12-31
Interventions
multifaceted nutrition interventionNutritional and Exercise Combined InterventionControl Group

Brief Summary

With world's older population is rapidly increasing. China's population aging process is also accelerating. Studies have shown that persistent frailty can increase the incidence of negative events in the elderly. However, research on elderly frailty in China is still in its early stages, and existing research in China mainly focuses on the definition of frailty, evaluation tools for frailty, and cross-sectional surveys of small populations. There is currently limited research on interventions. The MultIfaceted NUtrition inTErvention for Frailty (minute) trial is a randomized, controlled trial to explore the trajectory characteristics and influencing factors of frailty in the community, the impact of nutritional interventions on the developmental trajectory of frailty in the elderly in the community and the management model and appropriate technology for the sustainable intervention of frailty in the elderly based on the community. A total of 315 frail older adults will be recruited from Beijing. After the screening period, the compliant participants will be randomized to the control group, the nutrition intervention group with the nutrition intervention alone, or the combined nutrition intervention group with combining exercise and nutrition, on a 1:1:1 ratio, for 3 months. The primary outcome is the change in SPPB from the baseline to the end of the study. The change in SPPB as a primary outcome, and frailty status, demographic information, health status, nutrition assessment, comprehensive geriatric assessment status, quality of life, intrinsic capacity, and mental elasticity as secondary outcomes will be measured using validated questionnaires and clinical examinations. This trial adheres to the Declaration of Helsinki and guidelines of Good Clinical Practice. Signed informed consent will be obtained from all participants. The trial has been approved by the Peking University Institutional Review Board (approval number: IRB00001052-23178). The results will be disseminated through academic conferences and publications in international peer-reviewed journals.

Eligibility Criteria

Inclusion Criteria: 1. Frailty assessed by the frail phenotype 2. Aged between 65 and 85 years old Exclusion Criteria: 1. Multiple serious diseases such as stroke, cerebral infarction, tumors, and severe cardiovascular and cerebrovascular diseases 2. Disability, dementia; severe visual and hearing impairments, and physical activity impairment 3. Moderate to severe anxiety and depression 4. Unable to complete this study as requested

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