Development of a Research Registry for Possible Participation in Future Research Studies Conducted Within the IU Center for Alzheimer's Disease and Related Disorders

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Updated on 19 February 2024

Summary

The purpose of this Registry is to capture contact and personal health information data for self-referred volunteers and established clinical patients in the Indiana University Alzheimer's Disease and Related Disorders Center with the diagnosis of Probable Alzheimer's disease, Mild Cognitive Impairment, Lewy Body Disease, Frontal Temporal Dementia, Vascular Dementia and Parkinson's Dementia, who have interest in participating in various clinical research trials, either now or in the future.

Description

The purpose of this Registry is to capture contact and personal health information data for self-referred volunteers and established clinical patients in the Indiana University Alzheimer's Disease and Related Disorders Center with the diagnosis of Probable Alzheimer's disease, Mild Cognitive Impairment, Lewy Body Disease, Frontal Temporal Dementia, Vascular Dementia and Parkinson's Dementia, who have interest in participating in various clinical research trials, either now or in the future.

Participants will not be paid for their participation.
Participants will not be paid for their participation.
Participants will not be paid for their participation.

FAQ

Participants will not be paid for their participation.

Details
Condition Lewy Body Disease,Alzheimer’s disease,Frontal Temporal Dementia,Mild Cognitive Impairment,Vascular Dementia,Parkinson’s Dementia,healthy
Age 100years or below
Clinical Study IdentifierTX575
Last Modified on19 February 2024

Eligibility

How to participate?

Step 1 Connect with a study center
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If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.
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Enter your contact details to connect with study team

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Primary Contact

First name*
Last name*
Email*
Phone number*
Preferred way of contact label
Race
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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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