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Neural Mechanisms of Cognitive Assessment and Rehabilitation for Cognitive Decline

Neural Mechanisms of Cognitive Assessment and Rehabilitation for Cognitive Decline

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05014893
Enrollment
100
Registered
2021-08-20
Start date
2021-08-06
Completion date
2026-12-31
Last updated
2025-05-22

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

Conditions

Aging, Healthy, Mild Cognitive Impairment (MCI), Subjective Cognitive Decline (SCD)

Brief 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.

Detailed description

Cognitive assessment tools are used to assess cognitive function of subjects in different cities. Functional and structural MRI and EEG are applied to investigate the neural mechanisms of cognitive function decline and effects of methods to improve and restore cognitive function.

Interventions

COMBINATION_PRODUCTmulti-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)

Sponsors

Nanjing Brain Hospital
CollaboratorUNKNOWN
The Third People's Hospital of Yunnan Province
CollaboratorOTHER_GOV
Central South University
CollaboratorOTHER
Beijing academy of science and technology
CollaboratorUNKNOWN
Beijing University of Chinese Medicine
CollaboratorOTHER
National Research Center for Rehabilitation Technical Aids
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
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.

Secondary

MeasureTime frameDescription
Change in Physical capacity (TUG)Change from Baseline physical capacity test results at 3 months.The timed up and go (TUG) test is used to evaluate physical capacity of participants.
Change in Physical capacity (chair standing)Change from Baseline physical capacity test results at 3 months.The 30-second chair standing test is used to evaluate physical capacity of participants.

Other

MeasureTime frameDescription
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]Up to 24 months.Number of participants with treatment-related adverse events as assessed by CTCAE v5.0.

Countries

China

Contacts

Primary ContactYing Wang
CARM_AD@aliyun.com1058122921

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026