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Primary Care Detection of Cognitive Impairment Leveraging Health & Consumer Technologies in Underserved Communities: The MyCog Trial

NCT05607732

Active Not RecruitingNA

Sponsor: Northwestern University

Conditions: Dementia, Cognitive Impairment, Cognitive Decline, Alzheimer Disease

Interventions: MyCog

Countries: United States

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 overview

Sex: ALL

Age: 45 Years to —

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

Inclusion Criteria:

* been seen by an Oak Street healthcare provider affiliated with one of the 24 enrolled practices
* had at least one clinic visit (routine or Annual Wellness Visit) during the 3-year study period
* not 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.

Locations (1)

Chicago, Illinois, United States