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Combined exercise and cognitive intervention in Chinese older adults with mild cognitive impairment (COGITO): a home-based and remotely supervised intervention

Combined exercise and cognitive intervention in Chinese older adults with mild cognitive impairment (COGITO): a home-based and remotely supervised intervention

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073900
Enrollment
Unknown
Registered
2023-07-25
Start date
2023-08-01
Completion date
Unknown
Last updated
2024-03-18

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

Conditions

mild cognitive impairment

Interventions

intervention group:exercise, cognitive intervention, and health education
active control group 1:exercise and health education
active control group 2:cognitive intervention and health education
passive control group:health education

Sponsors

Peking University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Participants aged between 60 and 75 years old; 2. Participants were diagnosed as mild cognitive decline according to the Petersen criteria (Participants complained of memory loss for more than three months, which need to be proved by others. Objective memory decline that does not match age and educational level, and the overall cognitive function is basically normal. MMSE>17 for illiterate, MMSE>20 for primary school, MMSE>24 for junior high school and above. The score of GDS was 2-3. ADL was basically normal and the score in ADL was less than 14. No dementia (CDR=0.5)); 3. Participants have sedentary lifestyle in daily life; 4. Participants can understand the complete the intervention plan and the outcome assessment scales; 5. Participants sign an informed consent form and promise to have time to participate and complete the plan during the research; 6. Participants are not engaging in another intervention project currently; 7. Participants are accompanied by at least one family member or caregiver during the intervention; 8. Participants are living in the intervention area during the research.

Exclusion criteria

Exclusion criteria: 1. Participants developed nervous system diseases or orthopedic comorbidities and cannot conduct resistant training safely; 2. Participants has contraindications to aerobic exercise including confirmed heart disease and confirmed diabetes with poor control effect; 3. Participants use ß - Receptor blockers and/or antipsychotic medications; 4. Participants developed major depression, schizophrenia, and any form of mental illness or were confirmed severe neurological disorders in the previous year; 5. Participants developed Alzheimer's disease, infections of the central nervous system, post-traumatic dementia, toxic encephalopathy, metabolic encephalopathy, Huntington's disease, multiple sclerosis or Parkinson's disease before memory loss; 6. Participants were unable to complete simple smartphone operations; 7. There was no smartphone or Internet at home; 8. Participants did not have free time over 10% of 3 months; 9. Participants did not pass the health screening questionnaire before exercise training.

Design outcomes

Primary

MeasureTime frame
global cognitive function;

Secondary

MeasureTime frame
Activities of daily living;Quality of life;Fatigue;Frailty;Body function, ADL;Intrinsic capacity;Sleep quality;

Countries

China

Contacts

Public ContactYanan Luo

Department of Global Health, School of Public Health, Peking University

luoyanan@bjmu.edu.cn+86 185 1962 1115

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026