Robotic rehab may retrain the brain's sense of vertical after stroke
NCT ID NCT07023770
First seen Sep 01, 2026 · Last updated Sep 02, 2026 · Updated 1 time
Summary
This trial tests whether a 3-week rehabilitation program using an exoskeleton can help people who have had a stroke correct a condition called lateropulsion, where the body leans to one side due to a distorted sense of vertical. Participants will receive 15 sessions combining exoskeleton-assisted balance exercises with physiotherapy focused on upright orientation. The study measures changes in how accurately participants perceive verticality, which is key to balance and walking.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A 3-week rehabilitation program combining exoskeleton-assisted balance and gait exercises with physiotherapy focused on vertical body orientation.
- What this could lead to
- If it works, this could point toward a more effective rehab approach to help stroke survivors with lateropulsion regain balance and upright posture.
- What could go wrong
- This is a very small pilot study with only 3 participants, so results may not apply broadly. The program is intensive and may not be feasible for all stroke patients.
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
-
About 3 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Nov 2025
- Expected to finish
-
Nov 2026
An estimate. End dates often move.
- 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
-
18 to 84 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 Hide 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: * Right hemispheric first and unique ischemic stroke between 2 weeks and 6 months old (subacute phase) ; * Presence of lateropulsion, assessed by the Scale for Contraversive Pushing (2 ≤ SCP \< 5) * Presence of contralesional VV bias (VV \> 4°) * Right handedness defined by a Edinburgh score ≥0,39 * Being hospitalized in a Physical Medicine and Neurological Rehabilitation (PMR) facility. * Have given a written and informed consent Exclusion Criteria: * Medical instability making evaluation impossible, * Comprehension or cognitive or behavioral disorders, or depressive symptoms that compromise participation in the program * Postural disorders or body geometry disorders that interfere with balance for a reason that is independant of the stroke * Morphological contraindications to the use of the Atalante® robot (segment length or joint ranges; height \<155cm; weight \>100kg), * Severe spasticity (\>3 on the modified Ashworth scale) in the adductors, quadriceps, hamstrings and triceps surae * Presence of a pressure sore at the areas of contact with the Atalante® robot, * History of osteoporotic fractures. * Pregnancy and breastfeeding
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Stroke, ischemic are added.
By submitting, you agree to our Terms of use
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
2 sites. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Grenoble University Hospital
RECRUITINGÉchirolles, France
-
Grenoble University Hospital
RECRUITINGGrenoble, 38043, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- A multicenter, randomized, double-blind, placebo-controlled, parallel-group phase ⅱb/ⅲ clinical study to evaluate the efficacy and safety of XY03-EA tablets in the treatment of acute ischemic stroke
- AI may forecast stroke outcomes and guide recovery
- Retraining the brain to see again: a new hope for Stroke-Related blindness
- Can immune cells heal the heart and brain after attack?
- Can a gentle ear zap supercharge stroke rehab at home?
- Magnetic pulses to the brain may help stroke survivors regain arm function