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Huaxi-UBC Artificial Intelligence and Brain Health Research Project

Huaxi-UBC Artificial Intelligence and Brain Health Research Project

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035012
Enrollment
Unknown
Registered
2020-07-27
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-08-03

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

Conditions

Cognitive dysfunction, Alzheimer's disease, sarcopenia, weakness, disability, etc.

Interventions

Control group:health education
Intervention group:Joint intervention (exercise + nutrition + cognitive training)

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. A community resident between 65-75 years old (based on ID card); 2. The chief complaint of forgetfulness (self-reported memory has deteriorated in the past five years), or memory deterioration confirmed by himself or his accompany during interviews; 3. Baseline MoCA score 24; 4. Lawton and Brody daily tool activity scale score > 6/8; 5. Education: graduated from high school and above; 6. Living in your own home instead of hospital or long-term care Institutions; 7. Visual and auditory: you can read and write by yourself; 8. Do not take anti-dementia drugs (such as donepezil, galantamine, etc.) in the near future or during the research period; 9. Sign the informed consent form to confirm that all participants have been informed of the trial Related content; 10. Able to walk 4 meters independently with or without a walker; PAR-Q + scale evaluation confirmed that the health status of the subjects has reached the level of participating in the relevant exercises of the experiment.

Exclusion criteria

Exclusion criteria: 1. During the 3 months prior to entering the study, they were engaged in moderate 2 degree exercise (such as brisk walking) for more than 60 minutes per week; 2. Diagnosed with any type of dementia; 3. Clinically suspected of having neurodegenerative diseases (eg, multiple sclerosis, Parkinson's disease, Huntington's disease, frontotemporal dementia), Instead of Alzheimers disease, vascular cognitive impairment, which causes cognitive impairment; 4. There is a high risk of adverse cardiovascular events during exercise, or it is unable to adjust activities according to the guidance of rehabilitation exercise experts or fail to pass Understand to reach the recommended level of activity; 5. Diagnosed with severe peripheral neuropathy or severe musculoskeletal or joint disease that impairs mobility; 6. Taking drugs that may have a negative impact on cognitive function, such as anticholinergic drugs, including Drugs with obvious anticholinergic properties (such as amitriptyline), main sedatives (ie typical and atypical antipsychotics) and anticonvulsants (such as gabapentin, sodium valproate); 7. Within the last 24 months Any hormonal therapy (estrogen, progesterone or testosterone) received; 8. Plan to participate in or have participated in a synchronized clinical drug or exercise test; 9. Elderly persons with metal in the body, including dentures (not removable), cardiac pacemakers, Artificial hip joints, steel plates, steel nails, brackets and other metals, so as not to affect the fMRI test results.

Design outcomes

Primary

MeasureTime frame
fMRI;step speed;Hand grip;BIA;Chair-sit-up-test;

Countries

China

Contacts

Public ContactBirong Dong

West China Hospital of Sichuan University

hxncrcg@163.com+86 18980601332

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026