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Enrolling By Invitation
NCT06542458
Under-Represented Communities Diagnosed With SCD or MCI Through Tele-Cog
Conditions: Mild Cognitive Impairment, Subjective Cognitive Decline
Sex: All
Ages: 50 Years – N/A
Healthy volunteers: No
Enrollment: 100
Sponsor: Ohio State University
Location: The Ohio State University Columbus Ohio
Summary
The purpose of this study is to establish a longitudinal cohort of older adults with Subjective Cognitive Decline (SCD) or Mild Cognitive Impairment (MCI): 1) at heightened risk for dementia, and 2) from underrepresented/under-resourced communities to characterize clinical course. This study will utilize the Tele-Cog clinic as a means for recruiting older adults at risk for dementia from under-resourced and underrepresented communities. Successful completion of this project will increase the opportunity for under-resourced and underrepresented communities to participate in cognitive research.
Eligibility Criteria
Inclusion Criteria:
1. Adults ages 50 years and older
2. Diagnosed with subjective cognitive concerns (SCD) or objective cognitive decline with mostly intact functioning (MCI diagnosis) as part of clinical work up
3. Fluent in English
4. Able to provide voluntary informed consent
5. Willing and able to undergo all study procedures
6. Able to delegate, if possible, a study partner. The study partner must be ≥18 years of age and must know the patient well enough to contribute information regarding the patient's daily activities and cognition.
7. Must also consent to the Neuroscience Research Institute Brain Bank and Biorepository (NRI-BBB) Banking Protocol (OSU protocol 2020H0512).
Exclusion Criteria:
1. Diagnosis of dementia at baseline.
2. Inability to give informed consent.
3. High risk of adverse emotional or behavioral reaction based on investigator's clinical evaluation (e.g., evidence of serious personality disorder, antisocial behavior, serious current stressors, lack of meaningful social support).
Source: ClinicalTrials.gov (NCT06542458). StuddyBuddy aggregates publicly available trial information.