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New rehab after botox aims to strengthen foot lift in stroke survivors

NCT ID NCT07260565

Symptom relief Sponsor: Clinique Victor Pauchet Source: ClinicalTrials.gov ↗

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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether a special strengthening and fatigue protocol using an isokinetic dynamometer can improve foot lift strength and walking more than standard rehab after Botox injections. Thirty adults with spastic foot drop will be randomly assigned to either the new protocol or usual therapy. The main goal is to see if foot lifter strength improves more with the new approach.

What this could mean

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

Active substance
botulinum toxin injection followed by isokinetic rehabilitation protocol
What this could lead to
If it works, this could point toward a more effective rehabilitation routine to improve walking and foot strength after Botox for spastic foot drop.
What could go wrong
This is a small, early-stage trial with only 30 participants, so results may not apply to everyone. The special protocol may not prove better than standard rehab.

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 30 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

Nov 2028

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 years and older

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: * Adult patient * Patient with spastic hemiplegia (regardless of cause) * MAS 1-2 spasticity of the plantar flexors * Deficit of the foot lifters at the minimum stage of contraction with movement * Patient who has received botulinum toxin injections in the plantar flexors * Patient who has been informed about the research and has given their written and signed informed consent * Patient affiliated with a social security scheme or beneficiary of such a scheme Exclusion Criteria: * Refusal of consent * Patient with severe cognitive impairment (MMSE \<23/30) * Surgery on the affected lower limb * Patient unable to read, write or understand French * Patient who is pregnant or breastfeeding, in accordance with Article L1121-5 of the CSP * Vulnerable patients according to Article L1121-6 of the CSP * Adult patients under guardianship, curatorship or judicial protection * Patients unable to give their consent in person according to Article L.1121-8 of the CSP or adults protected by law

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Conditions

The condition(s) this trial relates to.

spastic hemiplegia

As listed by the trial registrant

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

Spasticity of the plantar flexors

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  2. 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.

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