Effects of Local Vibrations Program of Dorsiflexor Muscles on Neuromotor Recovery in Subacute Stroke Patients.
Recruiting now · Not applicable · Has a placebo group
Conditions studied: Stroke Rehabilitation
In brief
The aim of the vibration intervention proposed in the current study is to allow a better neuromotor recovery in subacute stroke patients when compared with standard rehabilitation alone. These last years, it has been proven that the solicitation of a muscle using vibrations may lead to positive effects on the neuromuscular function. Thus, the aim of the current study is to assess if the addition to a standard rehabilitation program of local vibrations sessions of the dorsiflexor muscles of the paretic limb of stroke patients may allow a better recovery of walking speed (primary outcome). One group using vibrations (i.e. experimental group) and one group with sham vibration (i.e. control group) will take part to this study.
Key facts
- Study ID
- NCT05945212
- Run by
- Centre Hospitalier Universitaire de Saint Etienne
- People needed
- 70
- Starts
- 2024-03-12
- Expected to finish
- 2027-05-15
- Last updated by the study team
- 2025-12-04
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Stroke patients in subacute rehabilitation phase (between 14 days and 3 months post-stroke)
- Presenting with a stroke, ischemic or hemorrhagic
- Lower-limb deficiency with an initial motor testing < 4 according to the MRC scale
- No neurological history with functional impact other than stroke
- Having received informed information about the study and having signed the written consent
- Affiliated or entitled to a social security scheme.
- Patients under guardianship may be included; they may give their consent with the assistance of their guardian.
- If the participant is unable to write, their consent may be given and documented by other appropriate means in the presence of at least one impartial witness. In this case, the witness will sign and date the informed consent document.
You may not qualify if…
- Multiple stroke
- Other neurological, cognitive or psychiatric conditions
- Orthopedic ankle history compromising measurements
- Botulinum toxin injected in the lower limb prior the study protocol
- Patient with phlebitis or risk of thrombosis in the lower limb
- Patient under tutorship
Where it is running
- Hôpital Marrel — Rive-de-Gier, France (enrolling)
- Hôpital Bellevue, CHU de Saint-etienne — Saint-Etienne, France (enrolling)
- Centre Hospitalier Georges Claudinon — Le Chambon-Feugerolles, France
- Service de SSR du Centre Le Clos Champirol — Saint-Etienne, France
- Hospices Civils de Lyon, site Henry Gabrielle — Saint-Genis-Laval, France
- Service de SSR Val-Rosay — Saint-Didier-au-Mont-d'Or, France
- Centre Hospitalier de Roanne — Roanne, France
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.