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NCT07629674Recruiting

Visual Stimulation Through Video Therapy to Enhance Lower Limb Motor Recovery After Stroke

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)

Source: ClinicalTrials.gov · Last updated 13 Jul 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
12 (estimated)
First submitted
21 Jan 2026
Start date
9 Jul 2026
Primary completion date
31 Dec 2027
Lead sponsor
Centre Hospitalier Universitaire de Saint Etienne
Diseases
Stroke
NCT number
NCT07629674

What you commit to

  • Study type: Interventional
  • Planned participants: 12
  • From 9 Jul 2026 to the primary completion date, 31 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Severe general disabling medical conditions.
  • Associated cerebellar syndrome.
  • Major comprehension disorders, psychiatric illness, or cognitive impairments that could interfere with study participation.

Other

  • \- Severe hemispatial neglect.
  • Severe spasticity impairing proper positioning (Modified Ashworth Scale \> 3).
  • Participants under full legal guardianship (tutorship).
  • Pregnant or breastfeeding women.

Who the study is looking for

  • \- 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.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Service de Médecine Physique et réadaptation
Coordinator of this site? Confirm its status
Saint-EtienneFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.