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Under-Represented Communities Diagnosed With SCD or MCI Through Tele-Cog

NCT06542458 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2026-02-25

No results posted yet for this study

Summary

Overall, this study's primary aim is to establish a prospective, longitudinal, observational cohort study of older adults at risk for dementia from under-resourced/underrepresented communities. More specifically, older adults diagnosed with subjective cognitive decline (SCD) or Mild Cognitive Impairment (MCI) during clinical care offered via the Tele-Cog clinic would be recruited for more comprehensive data collection to characterize the clinical presentation and course of illness over multiple timepoints spread out longitudinally.

Conditions

Interventions

BEHAVIORAL

Assessments

Participants will undergo a standard battery of neuropsychological measures, behavioral questionnaire, and functional assessment to monitor cognition and function over time. Clinical data obtained as part of standard of care will be collected from the medical record

OTHER

Neuroimaging volumetric measures

Neuroimaging volumetric measures will be obtained from already conducted standard of care neuroimaging.

OTHER

Biofluid samples

Biofluid sampling data will be obtained through another protocol. All participants will be required to sign that consent to participate in this trial.

Sponsors & Collaborators

  • Ohio State University

    lead OTHER

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-12-01
Primary Completion
2032-01-01
Completion
2032-01-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06542458 on ClinicalTrials.gov