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Brain Activity Measures to Track Walking Recovery After Stroke With a Wearable Robot

Studies brain signals during walking with a wearable robot in adults after stroke.

Plain-language title generated from the registry record
Registry title: A Mobile Brain/Body Imaging Platform for the Assessment and Optimization of Post-stroke Overground Robotic Gait Treatments

Key facts

Where
Costa Masnaga, ItalySee the site

Where in Italy

  • Villa Beretta Rehabilitation CenterCosta Masnaga, ItalyTaking 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
Dr. Franco Molteni
Trial code
NCT07510633
Record updated
3 April 2026
Original description
The study aims to identify neural biomarkers that can be used to monitor the recovery of locomotion and movement of post-stroke patients, both in natural settings and with enriched treatment using robotic device. These biomarkers could potentially be utilized in clinical practice to improve recovery outcomes. Additionally, the study seeks to investigate whether it is feasible to use these biomarkers to predict the extent of recovery that patients may achieve.Read full original descriptionShow less

A Mobile Brain/Body Imaging Platform for the Assessment and Optimization of Post-stroke Overground Robotic Gait Treatments

The study aims to identify neural biomarkers that can be used to monitor the recovery of locomotion and movement of post-stroke patients, both in natural settings and with enriched treatment using robotic device. These biomarkers could potentially be utilized in clinical practice to improve recovery outcomes. Additionally, the study seeks to investigate whether it is feasible to use these biomarkers to predict the extent of recovery that patients may achieve.

Inclusion: Age ≥18 years old; Stroke patients with different etiology: ischemic or hemorrhagic; Able to walk independently, eventually with aids/orthosis (FAC>2); Able to give the informed consent and to comprehend the instructions necessary to complete the task; Subject's anthropometric parameters adequate to wear the exoskeleton; Body weight < 90 kg; Height 150 ÷ 192 cm; Thigh lenght: 355 ÷ 475 mm; Calf lenght: 405 ÷ 485 mm; Hip width : 690 ÷ 990 mm.

Exclusion: Incapacity to give the informed consent and understand the tasks required; Fixed contracture at lower limbs that limits the use of the exoskeleton; Incapacity to walk independently (FAC<=2); Subject's anthropometric parameters not adequate to wear the exoskeleton.

ClinicalTrials.gov NCT07510633