Viewing Study NCT04821635


Ignite Creation Date: 2025-12-24 @ 10:21 PM
Ignite Modification Date: 2026-02-25 @ 8:25 PM
Study NCT ID: NCT04821635
Status: WITHDRAWN
Last Update Posted: 2025-09-19
First Post: 2021-03-17
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Effects of FES-Rowing in Neurological Disorders (FES-ROW)
Sponsor: UGECAM Rhône-Alpes
Organization:

Study Overview

Official Title: Effects of Training on a Rower Assisted by Electrostimulation of Lower Limbs in Patients With Neurological Disorders (FES-ROW)
Status: WITHDRAWN
Status Verified Date: 2024-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: no participant enrolled
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: FES-ROW
Brief Summary: The main objective of this project is to measure the increase in aerobic physical and metabolic capacities with a 6-month training on a rower assisted by electrostimulation of lower limbs in a population of adults with traumatic paraplegia.
Detailed Description: Beyond the inability to walk, chronic paraplegic patients show an increase in their mortality from cardiovascular pathologies, compared to the same age groups of the general population. It is the hypoactivity induced by neurological impairment that is implicated in the first place in the pathogenesis of these abnormalities. The search for training methods adapted to these patients is justified to limit cardiovascular morbidity and mortality.

The aim of this project is to measure the increase in aerobic physical and metabolic capacities with a 6-month training on a rower assisted by electrostimulation of lower limbs in a population of adults with stabilized paraplegia (non-walkers), of traumatic origin.

Study is divided in two 3-month phases. The first consists on a training on a rowing machine with solicitation of the electrostimulated lower limbs only for a period of 3 months at the rate of 3 sessions of 30 minutes per week. The second consists on a training on a rowing machine with solicitation of the electrostimulated lower limbs and upper for a period of 3 months at the rate of 3 sessions of 30 minutes per week. The evaluations are composed of the measurement of maximum oxygen consumption, muscle and neurological parameters

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
2020-A00416-33 OTHER ID-RCB View