← Back to Clinical Trials
Recruiting NCT05908266

NCT05908266 Flexible Reaching Control in Parkinson Disease

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT05908266
Status Recruiting
Phase
Sponsor Université Catholique de Louvain
Condition Parkinson Disease
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2023-05-01
Primary Completion 2027-10-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 99 Years
Study Type OBSERVATIONAL
Interventions
Reaching movementsDisease Assessment

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 100 participants in total. It began in 2023-05-01 with a primary completion date of 2027-10-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Current research and theories have highlighted that the parameters linked to movement planning, e.g. the decision to select a movement goal, and adaptation, e.g. the ability to update control dependent on a novel dynamical context, are update quickly and within an ongoing movement in the general population. In parallel, it has been suggested that the evaluation of movement costs is a function of the basal ganglia, and it is impaired in Parkinson disease (PD). Here the investigators want to test whether these mechanisms also alter the ability of patients to update control during an ongoing action. A positive result would confirm that movement-related costs and dynamical representations depend on the integrity of the basal ganglia, in contrast a negative result would indicate that the deficit in PD is more specifically related to movement initiation, which would invite one to reconsider the cause of bradykinesia in this population.

Eligibility Criteria

Inclusion Criteria: * Ability to perform the task (assessed during the experiment) Exclusion Criteria: * Inability to perform the task (motor) or to understand the task requirements (cognitive)

Contact & Investigator

Central Contact

André Mouraux, PhD

✉ andre.mouraux@uclouvain.be

📞 +32 2 764 54 47

Principal Investigator

Frédéric Crevecoeur, PhD

STUDY DIRECTOR

Université Catholique de Louvain

Frequently Asked Questions

Who can join the NCT05908266 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 99 Years, studying Parkinson Disease. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05908266 currently recruiting?

Yes, NCT05908266 is actively recruiting participants. Contact the research team at andre.mouraux@uclouvain.be for enrollment information.

Where is the NCT05908266 trial being conducted?

This trial is being conducted at Louvain-la-Neuve, Belgium.

Who is sponsoring the NCT05908266 clinical trial?

NCT05908266 is sponsored by Université Catholique de Louvain. The principal investigator is Frédéric Crevecoeur, PhD at Université Catholique de Louvain. The trial plans to enroll 100 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology