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Robots may help children with hemiplegia take better steps

NCT ID NCT04246788

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 06, 2026 · Last updated Aug 07, 2026 · Updated 1 time

Summary

This trial tests whether intensive robot-assisted gait training can improve walking in children with hemiplegia, a form of cerebral palsy affecting one side of the body. Children aged 4 to 18 will receive either robot-assisted sessions with the G-EO system or standard physiotherapy. The study measures changes in walking speed, endurance, and joint movement to see if the robotic approach offers an advantage.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Intensive robotic rehabilitation using the G-EO system
What this could lead to
If effective, this could offer a new, more intensive way to improve walking ability and independence in children with hemiplegia.
What could go wrong
This is a small, early-stage trial, and the robot's benefit over standard physiotherapy is not yet proven. Results may not apply to all children with hemiplegia.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

40 people

The number who actually took part.

Started

Jul 2020

Finished

Nov 2021

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

4 to 18 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Hemiplegic children aged from 4 to 18 years * GMFCS (Gross Motor Function Classification System) score between I and III with lower limb involvement. * Children must walk alone with or without aid at least 10 meters, must have acquired sitting position, must be able to understand simple orders to follow the rehabilitation program. * Free and informed consent of holders of parental authority and of the patient * Affiliated to the social security system Exclusion Criteria: * No lower limb involvement, * spasticity = 4 on the modified Ashworth scale, * severe cardiorespiratory disease forbidding the rehabilitation program, * orthopedic surgery or botulinic toxin injections in the last 6 months before the beginning of the study.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • CHU Clermont Ferrand

    Clermont-Ferrand, Auvergne, 63000, France