[Remote] Cognitive Impairment Registry

  • STATUS
    Recruiting
  • End date
    Dec 31, 2025
Updated on 23 November 2020

Summary

The purpose of this study is to develop a recruitment registry of potential drug study participants who may have amyloid, a specific biomarker for Alzheimer's disease, using a phone assessment of cognitive and behavioral functions. The investigator uses the responses to the phone questions to predict which participants most likely would show amyloid should they have a PET brain scan. An amyloid positive PET scan is required to enroll in the majority of Alzheimer drug studies.

Description

There is one phone call for the participant that takes 30 to 45 minutes and one optional phone call with a caregiver/ study partner that takes 30 minutes.

Details
Condition *Healthy Volunteers
Clinical Study IdentifierTX255756
Last Modified on23 November 2020

Eligibility

Yes No Not Sure

Inclusion Criteria

You are a male or female, 60 years or older and live in San Antonio, Texas or the surrounding areas
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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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