NCT05998265View on ClinicalTrials.gov

A Randomised, Controlled, Open-Label, Multi-Centre Study to Evaluate the Efficacy of FeetMe® Home-Bases Rehabilitation Program in Comparison to Conventional Physiotherapy in Patients With Parkinson's Disease Using Connected Insoles

NANot yet recruitingINTERVENTIONAL

Enrollment

150

Participants

Timeline

Start Date

November 30, 2023

Primary Completion Date

November 30, 2025

Study Completion Date

November 30, 2025

Conditions

Parkinson DiseaseGait Disorders, Neurologic

Interventions

DEVICE

FeetMe rehabilitation

Home based rehabilitation program with real time biofeedback using a connected device

OTHER

Physiotherapy

Conventional physiotherapy as prescribed by the neurologists

All Listed Sponsors

collaborator

University Hospital, Lille

OTHER

lead

FeetMe

INDUSTRY

NCT05998265 - A Randomised, Controlled, Open-Label, Multi-Centre Study to Evaluate the Efficacy of FeetMe® Home-Bases Rehabilitation Program in Comparison to Conventional Physiotherapy in Patients With Parkinson's Disease Using Connected Insoles | Biotech Hunter | Biotech Hunter