Actively Recruiting

Phase Not Applicable
Age: 45Years +
All Genders
NCT05607732

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

Led by Northwestern University · Updated on 2026-03-27

45257

Participants Needed

1

Research Sites

179 weeks

Total Duration

On this page

Sponsors

N

Northwestern University

Lead Sponsor

O

Oak Street Health

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 45Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Been seen by an Oak Street healthcare provider at one of the 24 enrolled practices
  • Had at least one clinic visit (routine or Annual Wellness Visit) during the 3-year study period
  • Not previously diagnosed with cognitive deficits, impairments, or dementias
Not Eligible

You will not qualify if you...

  • Children, adolescents, and younger adults are excluded because cognitive impairment in these groups is often due to causes other than age-related changes

AI-Screening

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Trial Site Locations

Total: 1 location

1

Oak Street Health

Chicago, Illinois, United States, 60617

Actively Recruiting

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Research Team

M

Michael S Wolf, PhD MPH

CONTACT

M

Morgan R Bonham, BS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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