← Back to all trials
Not Yet Recruiting
NCT05607732
Primary Care Detection of Cognitive Impairment Leveraging Health & Consumer Technologies in Underserved Communities: The MyCog Trial
Conditions: Dementia, Cognitive Impairment, Cognitive Decline, Alzheimer Disease
Sex: All
Ages: 45 Years – N/A
Phase: NA
Enrollment: 45257
Sponsor: Northwestern University
Summary
Our study intends to offer 'real world' evidence of a viable, sustainable means to mobilize primary care via a comprehensive strategy for detecting cognitive impairment and dementias, advancing next steps for referral, and participating in the care planning and management of affected patients and caregivers.
We will conduct a clinic-randomized, pragmatic trial testing the effectiveness and fidelity of our NIH Toolbox-derived paradigm to improve early detection and management of cognitive impairment/dementia in primary care settings serving health disparate patient populations.
Eligibility Criteria
Inclusion Criteria:been seen by an Oak Street healthcare provider affiliated with one of the 24 enrolled practiceshad at least one clinic visit (routine or Annual Wellness Visit) during the 3-year study periodnot been diagnosed previously with cognitive deficits, impairments or dementias.Exclusion Criteria:Children, adolescence, and younger adults are excluded as cognitive impairment in these populations is often due to differences other than age-related changes.
Source: ClinicalTrials.gov (NCT05607732). StuddyBuddy aggregates publicly available trial information.