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Effect of Multicomponent Intervention on Functional Decline in Chinese Elderly (MIFDCE)

Effect of Multicomponent Intervention on Functional Decline in Chinese Elderly (MIFDCE)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040328
Enrollment
Unknown
Registered
2020-11-28
Start date
2020-12-10
Completion date
Unknown
Last updated
2021-02-16

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

Conditions

Functional decline in elderly

Interventions

Experimental group:Multicomponent intervention
Control group:Routine care

Sponsors

Jiangsu Province Hospital (The First Affiliated Hospital of Nanjing Medical University)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged 65-90 years old; 2. Barthel index > 60 (mild impairment of function, basic self-care, able to complete part of daily activities independently, and a small part of them need to be taken care of by others); 3. Walk independently (using assistive device), stable health condition and smooth communication with researchers; 4. Voluntarily sign informed consent; be able to cooperate with the smooth implementation of the whole project; 5. Patients can be followed up for more than 12 weeks.

Exclusion criteria

Exclusion criteria: 1. Unable to cooperate to complete assessment and intervention: extremely severe cognitive impairment (global decline scale, level 7), paralysis, etc; 2. Patients with high risk in the process of assessment and intervention: end stage of disease; severe dysfunction of important organs such as heart, lung and kidney; uncontrolled serious arrhythmia; acute pulmonary embolism; recent myocardial infarction and unstable angina pectoris; recent major surgery or limb fracture in the past three months; and; 3. Poor compliance, difficult to follow-up and unwilling to sign informed consent; 4. Other conditions or events that the researcher thinks should be excluded.

Design outcomes

Primary

MeasureTime frame
SPPB;ADL;

Secondary

MeasureTime frame
IADL;Tinetti;FRAIL;MNA-SF;MMSE;GDS-15;SF-12;4 meter pace;6-minute walk test;grip;BIA related data;

Countries

China

Contacts

Public ContactJianqing Wu

Jiangsu Province Hospital (The First Affiliated Hospital of Nanjing Medical University)

jwuny@njmu.edu.cn+86 13851659099

Outcome results

None listed

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