Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06230796
Other study ID # 2023-01-VR
Secondary ID 2023-A00627-38
Status Recruiting
Phase N/A
First received
Last updated
Start date November 17, 2023
Est. completion date December 1, 2025

Study information

Verified date January 2024
Source UGECAM Rhône-Alpes
Contact julie Di marco, MD
Phone 01133472532161
Email dr.jdimarco@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To determine whether active cycling assisted by functional electrical stimulation (FES) Is more effective than active cycling on cardiovascular fitness in post stroke hemiparesis


Description:

Design: In a monocentric, single-blind, randomized, controlled trial, hemiparetic post stroke patients will be randomized to receive FES-induced cycling training or placebo FES cycling. Setting: Neurologic Rehabilitation Unit Interventions: 30 minutes of active leg cycling with or without FES applied to the paretic rectus femoris of quadriceps and to the biceps femoris and semitendinosus muscles and gluteus maximus, 3 times/weeks for 8 weeks. During training, participants will be seated on a FES-Cycle (Hepha Bike, Kurage): a cyclo-ergometer (Technogym) combined with a 8 channel controlled stimulator (Motimove-8). In addition to the assigned group treatment, subjects will perform their own standard rehabilitation program. Participants will be evaluated before training, after training, and at 3 month follow-up visit


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date December 1, 2025
Est. primary completion date June 1, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adults with Hemiparesis after an unilateral first ever stroke - Able to walk in security - Time since stroke within 3 months to 1 year - Sufficient cognitive function to understand and perform corresponding tasks Exclusion Criteria: - Any history of neurological disorders or cardiovascular instability - High spasticity on ankle, knee, hip muscles - Inability to exercise on a cyclo-ergometer - Pacemaker and other contraindications of the use of electrical stimulation

Study Design


Related Conditions & MeSH terms


Intervention

Device:
FES-cycling
30 minutes of active leg cycling with or without FES applied to the paretic rectus femoris of quadriceps and to the biceps femoris and semitendinosus muscles and gluteus maximus, 3 times/weeks for 8 weeks. During training, participants will be seated on a FES-Cycle (Hepha Bike, Kurage): a cyclo-ergometer (Technogym) combined with a 8 channel controlled stimulator (Motimove-8).
SHAM-cycling
30 minutes of active leg cycling with SHAM FES applied to the paretic rectus femoris of quadriceps and to the biceps femoris and semitendinosus muscles and gluteus maximus, 3 times/weeks for 8 weeks. During training, participants will be seated on a FES-Cycle (Hepha Bike, Kurage): a cyclo-ergometer (Technogym) combined with a 8 channel controlled stimulator (Motimove-8).

Locations

Country Name City State
France SMR Val Rosay Saint didier au mont d'or

Sponsors (1)

Lead Sponsor Collaborator
UGECAM Rhône-Alpes

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary VO2 peak at 2 months (L/min) Comparison of the maximum oxygen consumption (VO2 peak in L/min) measured during an incremental maximum stress test on cyclo-ergometer between the end of training (M2) and inclusion (M0). From enrollment to the end of treatment at 8 weeks
Secondary Maximum power Comparison of the maximum power (in Watts) developed during the stress test on a cycloergometer between the end of the training (M2) and the inclusion (M0) 2 months
Secondary Walking ability walking speed (10m walking test) and distance (6-minute walking test) measured at inclusion, after training (M2) ans follow-up (M4) 4 months
Secondary quadriceps muscular thickness quadriceps muscular thickness measured with ultrasound at inclusion aand after the training 2 months
Secondary Middle Cerebral Artery Blood Flow Velocity During Exercise Middle Cerebral Artery Blood Flow Velocity During Exercise measured with transcranial Doppler ultrasound at inclusion (M0) and after the training (M2) 2 months
Secondary Cognitive function Paper test: Stroop and trail making test at inclusion and after training 2 months
See also
  Status Clinical Trial Phase
Completed NCT04323943 - Comparison of Thermo-plastic Versus Carbon Foot Ankle Orthosis to Improve Gait and Reduce Fatigue in Post-stroke Patients: a Biomechanical and Neurophysiological Study N/A
Completed NCT05062746 - Immediate Effect of One-session MRT in Hemiparetics N/A
Not yet recruiting NCT05626894 - Novel Wrist Sensor System to Promote Hemiparetic Arm Use in Home Daily Life of Chronic Stroke Survivors Phase 2
Recruiting NCT05399121 - Stroke Patients', Music Therapist' Engagement and Patients' Finger Movement During Music Therapeutic Interaction N/A
Recruiting NCT04620707 - RGS@Home: Personalized 24/7 Home Care Post-stroke N/A
Recruiting NCT05809037 - Evaluation of Noninvasive Vagus Nerve Stimulation on Functional Status in Ischemic Stroke N/A
Recruiting NCT06107010 - Effects of Atalante Exoskeleton on Gait Recovery in Non- or Poorly Ambulatory Patients With Hemiparesis in the Acute/Subacute Phase (Month 1 to 4) N/A
Terminated NCT05011448 - Correlation Between Music Therapist's and Stroke Patient's Engagement Levels and Patient's Fingers and Wrist Movement N/A
Active, not recruiting NCT04309266 - The Impact of Robot Assisted Therapy and Metacognitive Skills Training for Children With Hemiparesis N/A
Recruiting NCT05342688 - Contextual Interference, Engagement , and Change in Motor Performance in Stroke Phase 1
Recruiting NCT06362954 - The Relationship Between Muscle Oxygenation and Spasticity in Hemiparetic Stroke Patients
Recruiting NCT06109194 - Immediate Effect of Ankle Mobilization on Active Range of Motion and Gait in Subacute Stroke N/A
Recruiting NCT06140381 - Strengthening in Sub-acute Stroke Survivors: A Randomized Controlled Trial N/A
Completed NCT04314830 - Gait Perturbations to Improve Balance Post-stroke N/A
Completed NCT05097391 - Effectiveness of Paretic Lower Limb Loading During Over-ground Training Among Stroke Survivors N/A