Actively Recruiting
The Construction of a Digitally-Enabled Precision Assessment and Intervention System for Disability Risk in Older Adults and a Full-Cycle, Multi-Scenario Demonstration Study
Led by Second Affiliated Hospital, School of Medicine, Zhejiang University · Updated on 2026-04-02
238
Participants Needed
1
Research Sites
8 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying disability risk in older adults to identify key factors that lead to disability and to develop a precise, digital system for early warning and prevention. This study integrates multiple data sources, including health records and cognitive assessments, to build a risk stratification model and an intelligent early warning system. The goal is to create a collaborative hospital-community-household system that actively manages disability risk in diverse urban and rural settings. The study involves implementing a digital platform that provides comprehensive assessments, dynamic monitoring, and targeted interventions for disability risk in older adults. Participants are randomly assigned to either an experimental group receiving these digital interventions or a control group receiving routine community-based health management like health education, exercise guidance, and dietary counseling. Participants will be involved for at least six months, with assessments at the start, three months, and six months after intervention. These include physical performance tests, disability risk scoring, and monitoring of intervention adherence. The study measures outcomes such as physical function, incidence of disability, and compliance with interventions to evaluate the effectiveness of the digital system in managing disability risk.
CONDITIONS
Brief Title
A Digitally-Enabled System for Precision Assessment and Intervention of Disability Risk in Older Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Community-dwelling permanent residents aged 65 years or older
- Able to operate a smartphone independently or with help from a primary caregiver
- Clear consciousness with basic comprehension and communication abilities
- Voluntarily agree to participate and provide informed consent
You will not qualify if you...
- Unable to perform basic activities of daily living independently
- Significant cognitive or communication impairments
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 6 months
Participants receive either a digital platform-based intervention for comprehensive assessment, dynamic monitoring, and targeted prevention of disability risk, or routine community-based geriatric health management including health education, exercise guidance, and dietary counseling.
Visits at baseline, 3 months, and 6 months after intervention
Trial Site Locations
Total: 1 location
1
The Second Affiliated Hospital of Medical College of Zhejiang University
Hangzhou, Zhejiang, China, 310009
Actively Recruiting
Research Team
J
Jingfen Jin, Master
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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