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Find more clinical trials

Memory Aid App To Improve Cognition in People With Mild Cognitive Impairment

Start: Jan. 20, 2023
End: May 2024
Enrollment: 50

What Is This Study About?

This study will examine the effectiveness of a personalized, online training program to teach older adults with cognitive impairment how to use EMMA, a memory aid app. The EMMA app works on a computer or smartphone and is designed to support memory and healthy behaviors. In one month, all participants will complete six online training lessons to learn how to use EMMA, with access to technical support. Half of the participants will be randomly assigned to also receive brief phone check-ins with a clinician each week.  For the next three months, researchers will track how much the participants use the EMMA app. All participants will complete two phone interviews about their perceived cognitive skills, as well as thinking, memory, and daily functioning tests at the start of the study and after six months of using the app.

Do I Qualify To Participate in This Study?

Minimum Age: 50 Years

Maximum Age: N/A

Must have:

  • Self-reported cognition problems, based on questions at study screening
  • Able to read and speak English

Must NOT have:

  • Any medical, neurological, or psychiatric diagnosis that explains current cognitive issues (e.g., stroke)
  • Severe vision or hearing problems that would interfere with the completion of the study procedures

If I Qualify, Who Do I Contact?

Contact study personnel listed either under the general study contact or the location nearest you.

 
Study Contact
Maggie Dines, B.S.
Maureen Schmitter-Edgecombe, PhD

Need Help?

Contact NIA’s Alzheimer’s and related Dementias Education and Referral (ADEAR) Center at 800-438-4380 or email ADEAR.

Where Is This Study Located?

Washington
Washington State University - Pullman; Study Remote
Pullman, WA 99164-4820
Recruiting
Magaret Dines, B.S.

Who Sponsors This Study?

Lead: Washington State University

Collaborator Sponsor

  • United States Department of Defense

Source: ClinicalTrials.gov ID: NCT05696756

 

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