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Effectiveness of a multidimensional intervention program for elderly intrinsic capacity based on a digital platform: A study protocol for a randomized controlled trial

A study on the construction and application of a multi-dimensional intervention programme for intrinsic capacity of the elderly based on a smart platform

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109335
Enrollment
Unknown
Registered
2025-09-17
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-09-22

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

Conditions

intrinsic capacity

Interventions

intervention group:To receive a multidimensional intervention programme for intrinsic geriatric competence based on the Smart Platform, the broad content of which focuses on the development of the pro
control group:Receive routine health management, which includes assessing the physical condition of the elderly and providing corresponding health guidance and health education. Monthly telephone foll

Sponsors

Xuzhou Medical University Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 120 Years

Inclusion criteria

Inclusion criteria: 1. Individuals aged 60 and above; 2. Those with an initial ICOPE screening score of 1 or higher; 3. Individuals who are conscious, able to understand, and willing to cooperate in completing activities of daily living tests and assessments of cognitive and depressive symptoms; 4. Elderly individuals who can use smartphones; 5. Those who have been informed about the study and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Persons in an unstable state of illness or in the active phase of mental illness; 2. Those who suffer from severe bone and joint diseases, neuromuscular diseases, tumour malignancy and vascular dementia, traumatic brain dementia and other diseases that can significantly affect intrinsic ability; 3. those who are unable to cooperate in completing the questionnaire due to various reasons (acute illness, severe cognitive dysfunction, blindness, deafness, non-Chinese speaking, etc.); 4. those who do not agree to participate in the study.

Design outcomes

Primary

MeasureTime frame
cognitive;locomotor;vitally;psychoiogical;sensory;

Secondary

MeasureTime frame
Self-maintenance;quality of life;E-Health Literacy;

Countries

China

Contacts

Public ContactTang Xianping

Xuzhou Medical University Affiliated Hospital

15252083537@163.com+86 152 6201 8786

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 23, 2026