Brain chemical dopamine may hold key to preventing falls in seniors

NCT ID NCT06587217

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This completed study looked at whether the brain chemical dopamine helps older adults maintain fast walking speed despite age-related changes. Five participants aged 60 and older with mild parkinsonian signs took carbidopa and carbidopa-levodopa for 10 days. Researchers measured walking speed using sensors to see if boosting dopamine improves mobility.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Carbidopa and carbidopa-levodopa (Sinemet)
What this could lead to
If successful, this could point toward a treatment to improve walking and reduce fall risk in older adults with mild parkinsonian signs.
What could go wrong
This is a very small, early-phase study with only 5 participants, so results may not apply to the general population. The drugs used can cause side effects like nausea or dizziness.

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

Phase 1/2

Runs two stages together: safety and dose first, then whether the treatment works.

Participants

5 people

The number who actually took part.

Started

Oct 2024

Finished

Apr 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

60 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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age 60 or older (M/F) * Evidence of mild parkinsonian signs (incl. slow gait (\<1m/s)) Exclusion Criteria: * Evidence of prior established diagnosis and/or treatment for PD. * Presence of clinically significant degenerative joint disease and/or neuropathy interfering with proper assessment of the motor exam. * Presence of significant dementia. * History of stroke with residual clinical deficit interfering with walking. * For optional MR imaging only: Participants in whom magnetic resonance imaging (MRI) is contraindicated including, but not limited to, those with a pacemaker, presence of metallic fragments near the eyes or spinal cord, or cochlear implant. * For optional brain imaging only: Severe claustrophobia precluding neuroimaging procedures. * Participants that have been on monoamine oxidase inhibitors (MAOIs) within 2 weeks prior to starting study. * Inability to stand or walk without an assistive device * Hypersensitivity to the carbidopa, levodopa, and tablet components. * History of myocardial infarction (MI) with residual arterial, nodal or ventricular arrhythmia * History of peptic ulcer * Chronic wide angle glaucoma * Narrow angle glaucoma * Major psychotic disorder * Severe cardiovascular or pulmonary disease, bronchial asthma, renal, hepatic or endocrine disease * Subjects on dopamine D2 receptor antagonists, dopamine depleting agents, and metoclopramide. * Any other medical history determined by investigators to preclude safe participation.

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As listed by the trial registrant

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Contacts and locations

Locations

  • Domino&#39;s Farms

    Ann Arbor, Michigan, 48105, United States

  • University Hospital

    Ann Arbor, Michigan, 48109, United States