Could a tailored supplement boost nutrition while preserving Parkinson's drug power?
NCT ID NCT06954662
First seen Aug 13, 2026 · Last updated Aug 14, 2026 · Updated 1 time
Summary
This trial tests whether a specialized amino acid supplement designed for people with Parkinson's disease can improve nutrition without interfering with their dopamine medication. Researchers will compare this supplement to a store-bought whey protein supplement and an inactive placebo. Participants, who are 55 or older and have been on stable dopamine medication for at least 3 months, will drink each supplement at separate visits. Blood samples will measure amino acid and levodopa levels, and researchers will also assess mood and movement.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Amino acid supplement and whey protein supplement
- What this could lead to
- If successful, this could point to a nutritional supplement that helps people with Parkinson's get better nutrition without reducing the effectiveness of their dopamine medication.
- What could go wrong
- This is a very early, small study with only 3 participants, so results may not apply broadly. The supplements could still interfere with medication absorption or cause digestive discomfort.
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
-
3 people
The number who actually took part.
- Started
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May 2025
- Finished
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Jul 2025
- 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.
- Ages
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55 years and older
- Sex
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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: * diagnosis of idiopathic Parkinson disease by patient report * 55 years or older * Has been using dopamine replacement medication (e.g. levodopa) for at least 2 years. * On a stable dose of dopamine replacement medication for at least 3 months with no plans for change in the next two months. Exclusion Criteria: * Apparent cognitive impairment as determined by phone screening (TICS) * Diagnosis of Parkinsonism or atypical Parkinson's Disease * Are prescribed a dopamine antagonist * Any unstable medical condition * Any known bleeding disorder or currently taking blood thinners * Using deep brain stimulation * Gastric or bowel resection surgery
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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
-
UConn Health, Clinical Research Center
Farmington, Connecticut, 06030-3805, United States
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