Development of a Research Registry for Possible Participation in Future Research Studies Conducted Within the IU Center for Alzheimer's Disease and Related Disorders
Investigation of Alzheimer's and Related Disorders List of Names and Health Information
Brief description of study.
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.
Detailed description of study
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.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Lewy Body Disease,Alzheimer’s disease,Frontal Temporal Dementia,Mild Cognitive Impairment,Vascular Dementia,Parkinson’s Dementia,healthy
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Age: 100 years or below
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Gender: All
Inclusion Criteria
Have a caregiver and be diagnosed with one of the following:
Probable Alzheimer
The purpose of this study is to collect contact and health information from volunteers and patients diagnosed with conditions such as Alzheimer's disease, Mild Cognitive Impairment, Lewy Body Disease, Frontal Temporal Dementia, Vascular Dementia, and Parkinson's Dementia. This registry helps identify individuals interested in participating in future clinical research trials.
Participants will be asked to provide their contact and personal health information. This data will be used to match them with relevant clinical studies they may join now or in the future.
- Who can participate: Individuals diagnosed with Alzheimer's disease, Mild Cognitive Impairment, Lewy Body Disease, Frontal Temporal Dementia, Vascular Dementia, or Parkinson's Dementia, who have a caregiver, are eligible to participate.
- Study details: Participants will need to provide their contact and personal health information for the registry. This information will help identify suitable research trials for future participation.