Could your morning coffee slow Huntington's?
NCT ID NCT03034122
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether caffeine intake is linked to how Huntington's disease progresses in people who have the gene but not yet symptoms. Researchers followed 77 participants, measuring brain volume changes and thinking skills over time. The goal was to see if caffeine might be a simple lifestyle factor that could influence the disease.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- caffeine (dietary)
- What this could lead to
- If caffeine is found to slow brain changes, it could point toward a simple dietary way to delay Huntington's symptoms.
- What could go wrong
- This is a small observational study, not a treatment trial. It cannot prove cause and effect, and results may not apply to everyone with Huntington's.
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
-
77 people
The number who actually took part.
- Started
-
Oct 2017
- Finished
-
Apr 2024
- Lead sponsor
-
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
premanifest HD subjects
- Ages
-
21 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * HD mutation carriers (\>36 CAG) * premanifest (total motor UHDRS \< 5) * estimated time to diagnosis between 3 and 10 years * adults older than 21 years (in order to exclude juvenile patients who begin the disease before 21 years) * informed consent signed * with a social protection Exclusion Criteria: * MRI contraindication * pregnant and lactating women * People under guardianship, trusteeship, deprive of freedom
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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
-
AH-HP La Pitié-Salpétrière
Paris, 75679, France
-
AH-HP, Hôpital Henri Mondor
Paris, France
-
CHU Montpellier
Montpellier, France
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CHU Pellegrin
Bordeaux, France
-
CHU Purpan
Toulouse, France
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CHU de Amiens
Amiens, France
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CHU de Angers
Angers, France
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CHU de Grenoble
Grenoble, France
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CHU de Nancy
Nancy, France
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Hôpital Roger Salengro, CHRU
Lille, France
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