Web-Based Assessment Validation and Engagement Study

  • STATUS
    Recruiting
Updated on 13 October 2021
Investigator
Alyssa De Vito
Primary Contact
Online Study Center (online study) Contact
cognitive impairment
mild cognitive impairment
cognitive assessment
Online studies
Accepts healthy volunteers

Summary

This study is looking for people who are over the age of 55 and have mild cognitive impairment or dementia. The study is also looking for people with normal cognition, as a comparison. The study is investigating a new computerized assessment.

Description

Study schedule:
-The first study visit takes 1.5-2 hours. It involves completing questionnaires and doing a computerized assessment.
-About 2 weeks later, you can return for another study visit. It will take about an hour. You will complete the computerized assessment.

Study activities may include:
-Completing questionnaires about your cognition and well-being.
-Using a computer.
-Doing computerized assessments about your cognition and well-being.

Treatment or experiment details:
-There is no treatment or experiment being tested in this study.
-This study is interested in whether the computerized assessment is a useful tool, when compared to standard questionnaires.

Additional details:
-You will receive $50 after completing each visit.

Details
Condition *Healthy Volunteers, Mild Cognitive Impairment, Dementia
Clinical Study IdentifierTX249131
Last Modified on13 October 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Age 55 or older
Cognitively healthy, or have mild cognitive impairment or dementia
Clear my responses

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.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

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.

Learn more

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

Learn more

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