- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05908279
Gait Control in Parkinson Disease (GAIT-PD)
June 8, 2023 updated by: Université Catholique de Louvain
Flexible Control of Gait in Parkinson Disease: Effect of Task Instruction on the Exploitation of Redundancy in Speed Control.
Previous work has shown that a statistical property of gait characterised by long-range autocorrelation functions is altered in Parkinson disease (PD).
On the other hand it has been suggested that the same property is linked to the ability in healthy humans to co-regulate the amplitude and cadence of strides towards maintaining a constant speed.
Here the investigators want to better understand why it is altered in PD by measuring the transitions between gait instructed by a metronome, and gait without metronome.
The experimental conditions will allow the comparisons between these transitions across PD and healthy groups of volunteers, and assess differences based on statistical and computational modelling.
The link with potential freezing episodes will also be studied to assess whether the statistical determinants of gait control in this population can be used as a proxy or predictor of the occurence of freezing episodes.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: André Mouraux, PhD
- Phone Number: +32 2 764 54 47
- Email: andre.mouraux@uclouvain.be
Study Contact Backup
- Name: Frederic Crevecoeur
- Email: frederic.crevecoeur@uclouvain.be
Study Locations
-
-
-
Louvain-la-Neuve, Belgium, 1348
- Recruiting
- Université Catholique de Louvain
-
Contact:
- André Mouraux, PhD
- Phone Number: +32 2 764 54 47
- Email: andre.mouraux@uclouvain.be
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
One group of volunteers with previous diagnosis of Parkinson disease and one group of age and sex matched healthy volunteers.
Description
Inclusion Criteria:
- Patients and volunteers able to walk for 20mins and without other neurological disorders.
Exclusion Criteria:
- Patients or volunteers unable to walk for 20mins and with other neurological disorders.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Control
Healthy volunteers
|
Walk with and without a metronome
|
|
PD
Patients with Parkinson's disease
|
Walk with and without a metronome
Disease stage assessed by a doctor
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stride cadence
Time Frame: Measured during the entire experiment (an average of 4.5 years)
|
Time between two consecutive heel strikes.
Units are seconds.
|
Measured during the entire experiment (an average of 4.5 years)
|
|
Stride amplitude
Time Frame: Measured during the entire experiment (an average of 4.5 years)
|
Distance between two consecutive heel strikes.
Units are meters.
|
Measured during the entire experiment (an average of 4.5 years)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Frederic Crevecoeur, Université Catholique de Louvain
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 1, 2023
Primary Completion (Estimated)
October 31, 2027
Study Completion (Estimated)
October 31, 2027
Study Registration Dates
First Submitted
May 25, 2023
First Submitted That Met QC Criteria
June 8, 2023
First Posted (Estimated)
June 16, 2023
Study Record Updates
Last Update Posted (Estimated)
June 16, 2023
Last Update Submitted That Met QC Criteria
June 8, 2023
Last Verified
June 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GAIT-PD
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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