Can estrogen rewire how the brain learns fear?
NCT ID NCT07737613
First seen Jul 30, 2026 · Last updated Jul 31, 2026 · Updated 1 time
Summary
This study explores whether estrogen influences how the brain processes fear, focusing on postmenopausal women who experience natural declines in the hormone. Participants will take an estradiol tablet and undergo brain scans while viewing shapes that sometimes predict a mild electric shock. The goal is to understand how hormones and cognition together affect fear learning and anxiety risk later in life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- estradiol (a form of estrogen) given as an oral tablet
- What this could lead to
- If it works, this could point toward ways to reduce anxiety and PTSD risk in older women by understanding how estrogen influences fear processing.
- What could go wrong
- This is a very early, small study focused on brain activity, not on treating any condition. Results may not lead to practical changes.
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.
- Phase
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Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2027
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.
- Ages
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60 years and older
- 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: * post-menopausal * normal or corrected-to-normal vision * English speaking * stable medication use (no changes in the past three months) Exclusion Criteria: * use of hormone therapy containing synthetic estrogen * MRI contraindications (e.g., irremovable ferrous metal in body, claustrophobia) * history of neurological disorder (including mild cognitive impairment) or moderate to severe traumatic brain injury * use of antipsychotic, opiate, or mood stabilizer (i.e., lithium) medication * history of blood clots/deep vein thrombosis, prior stroke or TIA, uncontrolled hypertension * history of migraine with aura * severe liver disease * history of breast, endometrial, or ovarian cancer * smoking \>10 cigarettes/day
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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 official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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.
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