NCT07508813

Brief Summary

  1. 1.Identify the primary risk factors for disability in older adults through multi-dimensional risk factor screening.
  2. 2.Develop a risk stratification model for disability in older adults by integrating outcome indicators and temporal characteristics, and construct an intelligent early warning model to enable automated assessment and monitoring of disability risk.
  3. 3.Establish key digital technologies for early warning and prevention of disability risk in older adults, and develop a whole-process digital intervention platform incorporating a decision support system for disability prevention management.
  4. 4.Create a digitally empowered hospital-community-household collaborative system for precise assessment and intervention of disability risk in older adults, achieving data-driven whole-process active disability management. The system will be demonstrated and evaluated in communities with diverse characteristics across urban, county, and rural settings.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
238

participants targeted

Target at P75+ for not_applicable

Timeline
5mo left

Started Oct 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress65%
Oct 2025Dec 2026

First Submitted

Initial submission to the registry

September 24, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

October 31, 2025

Completed
5 months until next milestone

First Posted

Study publicly available on registry

April 2, 2026

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 31, 2026

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2026

Last Updated

April 2, 2026

Status Verified

September 1, 2025

Enrollment Period

1 year

First QC Date

September 24, 2025

Last Update Submit

March 30, 2026

Conditions

Keywords

older adultsdisabilitypreventionrisk

Outcome Measures

Primary Outcomes (1)

  • SPPB(SHORT PHYSICAL PERFORMANCE BATTERY PROTOCOL)

    the range of score is 0-12, and the higher scores mean a better outcome.

    At baseline, 3 months after intervention, and 6 months after intervention

Secondary Outcomes (3)

  • Incidence of disability

    6 months after intervention

  • Disability Risk Score

    At baseline, 3 months after intervention, and 6 months after intervention

  • Intervention adherence

    3 months after intervention, and 6 months after intervention

Study Arms (2)

Experimental group

EXPERIMENTAL

Implement a digital platform for elderly disability risk intervention to conduct comprehensive, multi-scenario intelligent assessments, dynamic monitoring, and targeted interventions for disability risks.

Other: Risk Assessment of Disability and Precision Intervention

Control group

NO INTERVENTION

Conduct routine community-based geriatric health management, such as health education, exercise guidance, and dietary counseling.

Interventions

Implement a digital platform for elderly disability risk intervention to conduct comprehensive, multi-scenario intelligent assessments, dynamic monitoring, and targeted interventions for disability risks.

Experimental group

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)

You may qualify if:

  • Community-dwelling permanent residents aged ≥65 years;
  • Able to operate a smartphone independently or with assistance from a primary caregiver;
  • Clear consciousness with basic comprehension and communication abilities;
  • Voluntarily agree to participate in the study and provide informed consent.

You may not qualify if:

  • Those who are unable to perform basic activities of daily living independently, or who have significant cognitive or communication impairments.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Second Affiliated Hospital of Medical College of Zhejiang University

Hangzhou, Zhejiang, 310009, China

RECRUITING

Study Officials

  • Jingfen Jin, Master

    The Second Affiliated Hospital of Medical College of Zhejiang University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Jingfen Jin, Master

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Nursing Depratment

Study Record Dates

First Submitted

September 24, 2025

First Posted

April 2, 2026

Study Start

October 31, 2025

Primary Completion (Estimated)

October 31, 2026

Study Completion (Estimated)

December 30, 2026

Last Updated

April 2, 2026

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

Locations