Everyday Needs Assessment for Cognitive Tasks (ENACT) Interview Study

  • STATUS
    Recruiting
  • End date
    Dec 31, 2024
Updated on 8 March 2023
Online studies
Accepts healthy volunteers

Summary

Researchers at the University of Illinois Urbana-Champaign are exploring challenges encountered in daily activities by older adults (60+) experiencing cognitive challenges. If you or someone you know is experiencing difficulty with thinking, memory, or concentration or has mild cognitive impairment, we would like to learn from your experiences to develop solutions. The long-term goal is to utilize this knowledge to increase technological innovations in the area of aging and cognitive impairment to support functional independence and promote quality of life.

Human Factors and Aging Laboratory
217-265-0885

Description

After an initial phone screening to determine eligibility, participants will complete two main parts of the study via Zoom: 1) an in-depth interview and 2) a set of questionnaires. Each part is expected to take a maximum of 2 hours. Participants will have the option to complete both in one day or split them into two different sessions. During the interview, participants will discuss their experiences with everyday activities (e.g., healthcare appointments, financial management, travel). The second portion will include surveys, questionnaires, and tasks that fall into three general categories: 1) basic background information, 2) social and community engagement, and 3) cognitive measures.


·       Have access to a computer and webcam
·       No history of significant psychological illness
·       No diagnosis of Alzheimer’s or other dementia

Details
Condition Mild Cognitive Impairment, Memory complaints, Traumatic Brain Injury, Post-stroke Cognitive Impairment
Clinical Study IdentifierTX254922
Last Modified on8 March 2023

Eligibility

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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