Could your brain help unlock Alzheimer's secrets?
NCT ID NCT00585572
First seen Aug 14, 2026 · Last updated Aug 14, 2026
Summary
This program collects brain and other tissue samples from adults, including healthy individuals and those with memory disorders, to support research on Alzheimer's disease. Participants are typically enrolled in affiliated studies or approved on a case-by-case basis. The goal is to advance scientific knowledge about how these diseases affect the brain.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this program could deepen understanding of Alzheimer's disease and related memory disorders, potentially guiding future treatments or preventive strategies.
- What could go wrong
- This is a tissue donation program, not a treatment trial, so it offers no direct health benefit to donors. Its impact depends on long-term research use and may not yield immediate findings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 9,999 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2007
- Expected to finish
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Aug 2050
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Participants agree to autopsy and brain/tissue/sample donation for research purposes only.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Is aged 18 years or older * Falls into one of the following categories: * Current or previous study participants involved in the ADRC Clinical Core, WRAP study, or other select ADRC-affiliated studies, or donors of special circumstance, including healthy controls, if approved on a case-by-case basis by the WBDP PI. Please note, ADRC-affiliated studies are not inclusive of ADRC-affiliated industry-sponsored studies. * Is a parent of either an ADRC Clinical Core or WRAP study participant, or is a spouse of a WRAP study participant. Exclusion Criteria: * VA research subjects * Subjects with a medical condition/disease that would exclude them from the spectrum of utility/interest to researchers as determined by a WBDP Neuropathologist: 1. Persons with Hepatitis B or C 2. Severe Traumatic Brain Injury 3. Positive CJD diagnosis 4. Persons with HIV/AIDS 5. Persons with brain tumors or blood clots that affect neurologic status, therefore creating a problem between diagnosing AD status and healthy status 6. Cancer that has metastasized to the brain 7. Radiation treatment to the head 8. Other infectious diseases that would be hazardous to staff handling the tissue 9. Prolonged ventilator dependency prior to death as determined by the Neuropathologist * Subjects who lack capacity to provide informed consent with no activated Power of Attorney (POA) for Healthcare, activated POA for Research, or legal guardianship (if not near death), or (if at or near death) have no spouse, parent, relative or friend willing/able to complete consent and other donation paperwork. * Subjects who otherwise have incomplete history or incomplete donation paperwork before a recovery can begin. * Subjects younger than 18 years of age. * An expected post-mortem interval (PMI) of greater than 16 hours for non-ADRC or non-WRAP participants. PMI is the time between death and the anticipated time of brain removal at autopsy. Families and recovery agencies are made aware of this time constraint when consenting for the recovery process. If a patient becomes ineligible due to PMI, the family and funeral home will be notified immediately. Diversions from this exclusion can be made by a WBDP PI or Co-PI. * Medical conditions that would put researchers at risk. * Other contingencies, as determined by the PI, that make enrollment impractical or unsafe. Note: It is anticipated, based upon the younger age of our study cohorts, that significant time may pass between WBDP registration and actual donation. The inclusion/exclusion criteria will be reviewed and applied at time of donation. As a result, donated tissue found to be unsuitable may be removed from the post-mortem tissue and biosamples collection.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Wisconsin Madison
Madison, Wisconsin, 53792, United States
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