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Development of a Clinical Risk Score Prediction Tool for 5-, 9-, and 13-year Risk of Dementia Among Late-life Population With Depression: a Longitudinal Cohort Study

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

The goal of this observational study is to learn about the ability of a point risk score prediction model, developed using electronic medical record data, to predict the risk of progression from geriatric depression to dementia in older Chinese adults. The main questions it aims to answer are: Does a higher point risk score increase the risk of developing dementia in older adults with depression? What is the accuracy of the point risk score prediction model in identifying individuals at high risk of dementia among older adults with depression? Participants will receive their usual medical care as they normally would. No new treatments, tests, or procedures will be performed specifically for this study. The research team will collect data from their electronic medical records, including depression diagnoses, dementia diagnoses, comorbidities, medication records, and follow-up information. The point risk score will be calculated based on these routinely collected clinical data.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Healthy Volunteers: t
View:

• Adults aged ≥50 years.

• A diagnosis of depression clearly recorded by a clinician in the electronic medical record at baseline (based on structured or unstructured diagnostic documentation formed through routine clinical practice).

• Complete baseline electronic medical record data available, including at least demographic information (age, sex), clinical diagnoses, comorbidities, and medication records.

• At least one follow-up record available in the electronic medical record system to enable determination of incident dementia outcomes.

• Informed consent provided for the use of routine medical data for this research analysis.

Locations
Other Locations
China
Second Affiliated Hospital of Nanchang University
RECRUITING
Nanchang
Contact Information
Primary
Xi-jian Dai, PhD
daixjdoctor@126.com
13755756959
Time Frame
Start Date: 2006-06-01
Estimated Completion Date: 2030-06-30
Participants
Target number of participants: 44
Treatments
Dementia Group
Participants who received a first diagnosis of dementia during the follow-up period. No study-specific intervention is administered; all participants receive routine clinical care as usual.
Non-Dementia Group
Participants with no diagnosis of dementia during the follow-up period. No study-specific intervention is administered; all participants receive routine clinical care as usual.
Related Therapeutic Areas
Sponsors
Leads: Second Affiliated Hospital of Nanchang University

This content was sourced from clinicaltrials.gov