Skip to content

Clinical efficacy of computerized cognitive training combined with aerobic exercise in older adults with mild cognitive impairment: a randomized controlled trial

Clinical efficacy of computerized cognitive training combined with aerobic exercise in older adults with mild cognitive impairment: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078266
Enrollment
Unknown
Registered
2023-12-01
Start date
2023-12-02
Completion date
Unknown
Last updated
2023-12-03

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

Conditions

mild cognitive impairment

Interventions

1:computerised cognitive training
3:computerized cognitive training combined with aerobic exercise

Sponsors

Shandong First Medical University&Shandong Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 95 Years

Inclusion criteria

Inclusion criteria: 1.Elderly people living permanently in Tai'an City and aged =60 years old; 2.Subjects are able to understand instructions and communicate normally with researchers; 3.The study subjects met the scientific diagnostic criteria of the Chinese Expert Consensus 2021 on the Diagnosis and Treatment of Mild Cognitive Impairment of Alzheimer's Disease Origin: ? Cognitive impairment of the study subjects with chief complaint or confirmed by a knowledgeable person; ? Objective evidence of impairment in 1 or more cognitive domains in the study subjects (based on a score of < 26 points on Montreal Cognitive Functioning Assessment Scale (MoCA), and 1 point was added to the total score when the number of years of education was = 12 years);? the subjects do not meet the diagnostic criteria for dementia (CDR = 0.5); ? the subject's ability to perform activities of daily living is basically intact (based on a score of < 23 on the Activities of daily living (ADL) scale); 4.Study subjects had adequate education (primary school education and above) and had the ability to read, write and communicate effectively before the onset of the disease; 5.Subjects signed an informed consent form and volunteered to participate in the study.

Exclusion criteria

Exclusion criteria: 1.Study subjects with well-defined psychiatric and neurological disorders (e.g. schizophrenia, alcohol dependence, substance abuse, cerebral haemorrhage, massive cerebral infarction, transient ischaemic attack, epilepsy, Parkinson's disease, etc.); 2.Subjects with a history of craniocerebral trauma, cerebrovascular disease, coma or general anaesthesia in the last 6 months; 3.subjects with severe visual and hearing impairments; 4.Subjects who have participated in other research projects to improve cognitive function within the last 3 months; 5.Subjects who could not cooperate with the cognitive examination; 6.Subjects with severe heart disease, fractures, partial or complete paralysis, and other conditions affecting motor function; 7.Subjects who have exercised regularly in the last 3 months, i.e., exercise frequency >3 days per week and effective exercise (i.e., heart rate maintained at 100-140 beats/min) for >30 min per session.

Design outcomes

Primary

MeasureTime frame
Global cognitive function;attention;memory;executive function;visuospatial function;

Secondary

MeasureTime frame
depression;apathetic;quality of life;

Countries

China

Contacts

Public ContactWenyue Zhang

Shandong First Medical University&Shandong Academy of Medical Sciences

zhangwenyueZ@163.com+86 156 6445 6950

Outcome results

None listed

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