NCT06395272Recruiting
Effects of Proprioceptive Sensitivity Stimulation Via the SURA Electrodevice on Kinematics, Kinetics and Spatiotemporal Parameters of Gait.
Effects of Proprioceptive Sensitivity Stimulation Via the SURA Electrodevice on Kinematics, Kinetics and Spatiotemporal Parameters of Gait: a Pilot Study.
Source: ClinicalTrials.gov · Last updated 14 May 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
Recovery of function in people with central nervous system (CNS) injury after stroke is very much like a relearning process that takes advantage of preserved sensorimotor circuits. Relearning can be optimised by providing appropriate proprioceptive (or deep sensory) information to the spinal cord with the aim of maximally engaging the preserved neural circuits. The development of the SURA electrodevice offers this sensitive input mechanism, within the Botton Up therapies. And through research on its use, the impact on the different dimensions related to gait and its components, and the translation to the functional reality of the person, will be evaluated.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 30 (estimated)
- First submitted
- 21 Apr 2024
- Start date
- 24 May 2024
- Primary completion date
- May 2025
- Lead sponsor
- Facultat de ciencies de la Salut Universitat Ramon Llull
- Diseases
- Stroke
- NCT number
- NCT06395272
What you commit to
- Study type: Interventional
- Planned participants: 30
- From 24 May 2024 to the primary completion date, May 2025
- 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
- Diagnosis of Cognitive, visual or cardiorespiratory disorder (including cardiac pacemaker placement, heart failure and arrhythmia)
- Balance disorders with vestibular features
- Skin diseases
Other
- Orthopaedic intervention for IE
- Botulinum toxin treatment within the last year.
- In addition, subjects who had participated in other studies in the last six months that could interact with the current study will be excluded.
Who the study is looking for
- Unilateral hemispheric stroke (ischaemic or haemorrhagic) diagnosed by MRI or CT scan, at least 3 months after onset of stroke
- Ability to walk at least 10m (irrespective of the need for assistance)
- Weakness in ankle dorsiflexion of the paretic limb (TFM\>3)
- Ankle ROM \>30° and 0° of foot dorsiflexion in knee extension
- Age between 18 and 85 years
- Mini-Mental State Examination (MMSE) \> 24 score, non-disabling cognitive impairment
- Presence of clonus and hyperresistance to passive joint movement.
Age in the registry: 18 years to 85 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CSSV-Rif Coordinator of this site? Confirm its status | Barcelona | Spain | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.