Pregnancy complication linked to midlife brain changes?
NCT ID NCT06640842
First seen Jul 14, 2026 · Last updated Jul 15, 2026 · Updated 1 time
Summary
This study investigates whether women who had high blood pressure during pregnancy (hypertensive disorders) show differences in brain health in midlife compared to those with normal pregnancies. Participants undergo MRI scans, blood tests, cognitive assessments, and sleep monitoring. The goal is to understand if these pregnancy complications are linked to later risks for dementia, heart disease, and cognitive decline.
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 it works, this could help identify early risk factors for dementia and heart disease in women with a history of hypertensive pregnancy.
- What could go wrong
- This is a small observational study with only 24 participants, so findings may not apply to all women. It looks for links, not causes.
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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24 people
The number who actually took part.
- Started
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Sep 2024
- Finished
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Jun 2025
- 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
Women who previously participated in the ADORE, received a hypertensive disorder diagnosis or had a healthy pregnancy during their participation.
- Ages
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18 to 54 years
- Sex
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Female participants only
- 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: * Participated in the ADORE trial ( R01 HD083292) Exclusion Criteria: * History of seizures or Epilepsy * Pregnant at screening * Ineligible to complete MRI due to metal in the body
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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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The University of Kansas Medical Center
Kansas City, Kansas, 66160, United States
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