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Clinical Trials in Belgium / NCT05908279
Recruiting Observational

Gait Control in Parkinson Disease

NCT05908279 · tracked via the Priya Life Science Belgium tracker
Phase
Observational
Started
2023-05-01
Last updated
2023-06-18

Condition(s) studied

Parkinson Disease

Investigational drug(s) / intervention(s)

Walking testDisease assessement

Walking test: Walk with and without a metronome

Disease assessement: Disease stage assessed by a doctor

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
99 Years
Healthy volunteers
Accepted
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.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Université catholique de Louvain Louvain-la-Neuve Belgium Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05908279 on ClinicalTrials.gov ↗ ← All trials in Belgium