Parkinson's patients try brain-boosting balance training to improve walking
NCT ID NCT05799690
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study is testing whether adding action observation and motor imagery (watching and imagining exercises) to standard dual-task gait training can improve walking and balance in people with Parkinson's disease who have trouble with posture and walking. 80 participants will be randomly assigned to one of two training groups, and researchers will use brain scans and blood tests to look for biomarkers that predict who responds best. The goal is to find better ways to personalize rehabilitation for Parkinson's patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- gait and balance training with dual-task plus action observation and motor imagery
- What this could lead to
- If successful, this could lead to more personalized rehabilitation programs for Parkinson's patients with walking and balance problems, potentially improving their mobility and quality of life.
- What could go wrong
- This is a small, early-stage study (80 participants) focused on finding biomarkers, not proving a treatment works. Results may not apply to all Parkinson's patients, and the training requires significant time and effort.
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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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2023
- Expected to finish
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Apr 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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45 to 85 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria for PD patients: * 45 years ≤ age ≤ 85 years; * Idiopathic PD according to the Movement Disorders Society (MDS) diagnostic criteria * Hoehn \& Yahr (H\&Y) score \<= 4 * PIGD phenotype * Stable dopaminergic medication for at least 4 weeks and without any changes during the observation period (28 weeks) * No dementia according to Litvan's criteria and Mini-Mental Status Examination score (MMSE) \>= 24 * No significant tremor/involuntary movements that could determine artifacts during the MRI acquisition * Oral and written informed consent to study participation Inclusion criteria for healthy controls: * sex-matched and age-matched (age range: mean age of PD years ± 15 years); * oral and written informed consent to study participation Exclusion criteria: * Medical conditions or substance abuse that could interfere with cognition; * Any major systemic, psychiatric, neurological, visual, and musculoskeletal disturbances or other causes of walking inability; * Contraindications to undergoing MRI examination; * Brain damage at routine MRI, including lacunae and extensive cerebrovascular disorders; * Denied oral and written informed consent to study participation.
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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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IRCCS San Raffaele
Milan, 20132, Italy
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Neurology Unit, Azienda Ospedaliera Universitaria Integrata di Verona
Verona, 37126, Italy
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