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Video therapy to help leg movement recovery after stroke

Tests video therapy alongside rehabilitation for leg weakness in adults after stroke.

Plain-language title generated from the registry record
Registry title: Visual Stimulation Through Video Therapy to Enhance Lower Limb Motor Recovery After Stroke

Key facts

Where
Saint-Etienne, FranceSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

Source: NCT07629674, who can take part

Where in France

  • Service de Médecine Physique et réadaptationSaint-Etienne, FranceTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Centre Hospitalier Universitaire de Saint Etienne
Trial code
NCT07629674
Record updated
13 July 2026
Original description
This pilot study evaluates video therapy for lower limb motor recovery after stroke, an approach remains insufficiently documented.Read full original descriptionShow less

Use of Intensive Visual Stimulation Through Video Therapy to Enhance Lower Limb Motor Recovery After Stroke (SIVIMI). A Single-Center Pilot Study Using a Single-Case Experimental Design (SCED)

This pilot study evaluates video therapy for lower limb motor recovery after stroke, an approach remains insufficiently documented.

This single-center pilot study uses a Single-Case Experimental Design (SCED) to evaluate the effects of intensive video therapy combined with conventional rehabilitation in patients with subacute or chronic post-stroke hemiparesis. Twelve participants will be included and allocated to different baseline durations according to a multiple-baseline SCED design.

The primary outcome is functional mobility, assessed using the Timed Up and Go (TUG) test, measured repeatedly throughout baseline, intervention, and follow-up phases.

Inclusion: - First or recurrent hemispheric ischemic or hemorrhagic stroke in the subacute or chronic phase (from 1 month to 1 year post-stroke); Currently receiving rehabilitation care in a Physical Medicine and Rehabilitation (PM\&R) department; Able to walk 3 meters back and forth, with or without an assistive device; Provided informed consent, signed jointly with the investigator.

Exclusion: Severe general disabling medical conditions; Associated cerebellar syndrome; Major comprehension disorders, psychiatric illness, or cognitive impairments that could interfere with study participation; - Severe hemispatial neglect; Severe spasticity impairing proper positioning (Modified Ashworth Scale > 3); Participants under full legal guardianship (tutorship); Pregnant or breastfeeding women.

ClinicalTrials.gov NCT07629674