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Study on the Effect of Different Doses of Computerized Cognitive Training on Cognitive Function in Patients with Mild Cognitive Impairment: An Open-Label, Randomized, Controlled Trial

Study on the Effect of Different Doses of Computerized Cognitive Training on Cognitive Function in Patients with Mild Cognitive Impairment: An Open-Label, Randomized, Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109560
Enrollment
Unknown
Registered
2025-09-22
Start date
2025-09-23
Completion date
Unknown
Last updated
2025-09-29

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

Conditions

Mild cognitive impairment

Interventions

Group 1:CCT Training, 30 minutes per session, 3 times a week, for a total of 12 weeks
Group 2:CCT Training, 45 minutes per session, 3 times a week, for a total of 12 weeks
Group 3:CCT Training, 60 minutes per session, 3 times a week, for a total of 12 weeks
Group 4:CCT Training, 30 minutes per session, 5 times a week, for a total of 12 weeks
Group 5:CCT Training, 45 minutes per session, 5 times a week, for a total of 12 weeks
Group 6:CCT Training, 60 minutes per session, 5 times a week, for a total of 12 weeks

Sponsors

Peking University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=60 years old; 2. Self-reported cognitive decline, and confirmed by an insider; 3. Score of 19 to 25 on the Montreal Cognitive Assessment (MoCA) scale (adjusted according to the years of education: 1 point for those with 6 years or less of education); 4. Maintain the ability to independently complete daily activities; 5. Possess basic communication skills and be able to cooperate in completing research. 6. Voluntarily participate in the research and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Suffering from underlying neurological diseases that may impair cognitive function, including but not limited to dementia syndrome, Parkinson's disease, epilepsy, cerebrovascular diseases, etc. 2. Suffering from severe or unstable organic diseases such as cancer, hydrocephalus, central nervous system tumors, or acute brain injury/infection; 3. Suffering from severe mental illnesses such as major depression, schizophrenia, schizoaffective disorder, bipolar disorder, etc. 4. There are severe visual or hearing impairments, or other physical conditions that may hinder the completion of the research; 5. Those who have participated in any other clinical trials within the past three months; 6. Have received transcranial magnetic stimulation (TMS), transcranial direct current stimulation (tDCS), phototherapy for any reason within the past six months, or have taken drugs that may significantly affect cognitive function (such as psychotropic drugs, psychoactive drugs, anticholinergic drugs, benzodiazepines, etc.); 7. There is a history of alcohol dependence or substance abuse; 8. Drinking alcohol or using other substances that affect cognitive function, such as coffee or cocaine, within 24 hours before the cognitive assessment; 9. The researcher believes that there are circumstances that are not suitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
MoCA scale score;

Secondary

MeasureTime frame
Mental health status at weeks 4, 12, and 24 post-randomization.;Cognitive performance in sub-domains at weeks 4, 12, and 24 post-randomization.;Functional activities at weeks 4, 12, and 24 post-randomization.;Change from baseline in MoCA scale scores at weeks 4 and 24 post-randomization.;

Countries

China

Contacts

Public ContactHaibo Wang

Peking University

624098727@qq.com+86 181 1878 5924

Outcome results

None listed

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