Kidney disease linked to faster memory loss, new study aims to find out why
NCT ID NCT04975464
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 600 people with and without chronic kidney disease (CKD) for up to four years to compare how often memory loss, confusion, and daily activity problems occur. Researchers will also look for risk factors that make thinking and memory worse in CKD patients. Participants undergo annual memory tests, medical interviews, and some have brain scans to understand the role of kidney health in brain function.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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600 people
The number who actually took part.
- Started
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Nov 2011
- Expected to finish
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May 2026
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
All potential participants must be previous BRINK participants
- Ages
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50 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 for CKD Participants: 1. In stages 3b-5 of chronic kidney disease (GFR ≤ 60 ± 5 ml/min/1.73m2) at the first baseline visit in BRINK 1.0. 2. Able to complete an approximately 90 minute cognitive and physical testing battery. 3. Able to sign the informed consent, or allow a caregiver, relative, surrogate, or witness to sign the informed consent if participant is unable to do so. Inclusion Criteria for non-CKD Participants: 1. GFR ≥ 60 ± 5 ml/min/1.73m2 at the first baseline visit in BRINK 1.0. 2. Able to complete an approximately 90 minute cognitive and physical testing battery. 3. Able to sign the informed consent, or allow a caregiver, relative, surrogate, and/or witness to sign the informed consent if participant is unable to do so. Exclusion Criteria: Exclusion Criteria for CKD and non-CKD Participants: 1. Acute psychiatric illness that would impede cognitive testing 2. Active chemical dependence 3. Legally blind or unable to complete cognitive tests due to visual loss or deafness
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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.
Contacts and locations
Locations
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Hennepin Healthcare Research Institute
Minneapolis, Minnesota, 55404, United States
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Minneapolis VA Healthcare System
Minneapolis, Minnesota, 55378, United States
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