multi-modal targeted intervention (e.g., cognitive training, exercise, games): The Intervention group will be given recommended interventions tailored to individuals based on their risks (e.g., physical exercise programs, cognitive training, dietary advice, control of blood pressure and cholesterol, healthy diet, control obesity, stop smoking,reduce alcohol excess)
Study summary
This study investigates the neural mechanisms of cognitive function decline, cognitive assessment methods for subjects with mild cognitive dysfunction (Mild cognitive impairment, MCI, or cognitive decline milder than MCI), and the approaches used to improve and restore cognitive function.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria:
* Adults being able to walk at least a block, and
* Adults with subjective cognitive decline (SCD), or
* Adults with mild cognitive impairment (MCI), or
* Adults with normal cognitive function
Exclusion Criteria:
* Clinical diagnosis of dementia
* Adults who cannot follow the protocal
Primary outcome measure(s)
Change in Cognitive function (SCD-9) — Change from Baseline Cognitive test results at 3 months. The SCD-9 questionnaire is used to assess cognitive function of participants.
Change in Cognitive function (MoCA) — Change from Baseline Cognitive test results at 3 months. The Montreal Cognitive Assessment test is used to assess cognitive function of participants.
Change in Cognitive function (AD8) — Change from Baseline Cognitive test results at 3 months. The AD8 test is used to assess cognitive function of participants.
Change in Cognitive function (CDR) — Change from Baseline Cognitive test results at 3 months. The Clinical Dementia Rating (CDR) test is used to assess cognitive function of participants.
Trial sites (1)
Facility
City
Region
Status
National Research Center for Rehabilitation Technical Aids
Beijing
Beijing Municipality
Recruiting
More National Research Center for Rehabilitation Technical Aids trials in China
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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