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Risk Prediction and Its Intelligent Assessment for Cognitive Impairment Among Community-dwelling Older Adults

Risk Prediction and Its Intelligent Assessment for Cognitive Impairment Among Community-dwelling Older Adults

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05385874
Enrollment
13228
Registered
2022-05-23
Start date
2022-04-01
Completion date
2023-12-30
Last updated
2024-04-04

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

Conditions

Aging, Cognitive Impairment, Cohort, Predictive Model

Brief summary

Cognitive impairment is one of the core early signs of dementia, and it is also a key stage for community-based dementia prevention. Accurate and convenient prediction of cognitive impairment can help the community to identify and manage the high-risk population of dementia. Previous studies had developed several dementia predicting models, but such models may be not suitable for cognitive impairment prediction. Based on the national representative follow-up data of Chinese Longitudinal Healthy Longevity Survey (CLHLS), this project aims to develop and validate a brief cognitive impairment prediction algorithm among the community-dwelling elderly, using machine learning methods (such as Logistic regression, Naïve Bayes model, Extreme Gradient Boosting Tree and so on). Finally, based on the constructed model, an easy-to-use online intelligent assessment tool for predicting cognitive impairment risk will be developed. The general practitioners, social workers and the elderly would be invited to use the tool and we will revise the tool according to their suggestions and comments. This project is expected to provide scientific basis and technical support for community-based dementia prevention, and will also be useful for the elderly to easily understand their cognitive health.

Interventions

None listed

Sponsors

Peking University Sixth Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

1. Aged 65 or over at baseline; 2. With normal cognitive function at baseline (score ≥ 18 on the Chinese version of Mini-Mental State Examination, MMSE); 3. Completed MMSE assessment three years later; 4. Provided informed consent voluntarily.

Exclusion criteria

1. Aged \<65; 2. had a history of dementia or MMSE score \< 18 at baseline; 3. lost to follow-up or without cognitive function assessment three years later; 4. Refused to participate the survey.

Design outcomes

Primary

MeasureTime frameDescription
AUCan average of 3 years after baseline assessementthe AUC of the prediciton model based on the test data

Secondary

MeasureTime frameDescription
positive predictive valuean average of 3 years after baseline assessementthe positive predictive value of the prediciton model based on the test data
negative predictive valuean average of 3 years after baseline assessementthe negative predictive value of the prediciton model based on the test data
sensitivityan average of 3 years after baseline assessementthe sensitivity of the prediciton model based on the test data
specificityan average of 3 years after baseline assessementthe specificity of the prediciton model based on the test data

Countries

China

Outcome results

None listed

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