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Promotion and application research for home exercise combined with virtual reality rehabilitation technology to intervene reversible cognitive frailty

Promotion and application research for home exercise combined with virtual reality rehabilitation technology to intervene reversible cognitive frailty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026686
Enrollment
Unknown
Registered
2019-10-18
Start date
2019-12-01
Completion date
Unknown
Last updated
2019-10-21

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

Conditions

Reversible Cognitive Frailty

Interventions

Exercise group:Exercise at home
Rehabilitation group:Rehabilitation at hospital
Exercise&Rehabilitation group:Exercise at home&Rehabilitation at hospital
control group:null

Sponsors

Huadong Hospital, Shanghai Medical College, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Reversible cognitive frailty patient: pre-physical frailty and physical frailty (Fried score 1-5); meanwhile, subjective cognitive decline (Spain SCD-Q score 0-7); 2. Aged 60-90 years; 3. MMSE 27-30; 4. Subjects capable of understanding the protocol, complying with its requirements, and attending study visits.

Exclusion criteria

Exclusion criteria: 1. Disability or handicap; visual or hearing impairments in compatible with performance and/or interpretation of neuropsychological tests; 2. Other primary psychiatric/neurologic disorders,such as AD;severe depression or generalized anxiety; acute infection diseaseacute traumatic brain injuries, stroke(< 3 months), autoimmune disease, multiple organ failure, which could be life-threatening in the short term; 3. Missing informed consent; 4. No readiness to save and refer pseudonym personal data; 5. Any condition disturbing or making MRI and other measures impossible; 6. Alcohol or drug abuse; 7. Participation in any clinical trial < 3 months prior to screening or ongoing other clinical trials; 8. Other situation that researchers considered not suite to be included.

Design outcomes

Primary

MeasureTime frame
subjective cognitive decline questionaire;Fried physical frailty score;

Secondary

MeasureTime frame
NIA-AA MCI criterian;Mini-Mental State Examination;

Countries

China

Contacts

Public ContactRuan Qingwei

Huadong Hospital, Shanghai Medical College, Fudan University

13661717346@163.com+86 13661717346

Outcome results

None listed

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