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NCT06968923Recruiting

Effectiveness of a Home-Based Rehabilitation Program in Stroke Survivors Using the Euleria Home® Device

Effectiveness of a Home-Based Rehabilitation Program in Stroke Survivors Using the Euleria Home® Device: A Crossover Study.

Source: ClinicalTrials.gov · Last updated 13 May 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

To verify the non-inferiority, in terms of post-treatment (T1) clinical effectiveness, of a "multidomain" telerehabilitation (TR) protocol compared to conventional outpatient rehabilitation in patients with stroke sequelae, with respect to motor, cognitive, and language functions. The absence of statistically significant differences between the two groups regarding treatment effects for each targeted domain will be considered an indicator of non-inferiority.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
90 (estimated)
First submitted
5 May 2025
Start date
26 Apr 2018
Primary completion date
29 Apr 2025
Lead sponsor
Universita di Verona
Diseases
Stroke
NCT number
NCT06968923

What you commit to

  • Study type: Interventional
  • Planned participants: 90
  • From 26 Apr 2018 to the primary completion date, 29 Apr 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

  • Contemporanea partecipazione ad altri studi clinici;
  • Decadimento cognitivo
  • Deformità ossee come conseguenza di precedenti eventi traumatici ai 4 arti;
  • Contratture fisse ai 4 arti valutate come 4/4 alla scala di Ashworth modificata (MAS)
  • Altre patologie neurologiche e ortopediche in grado di interferire con lo studio.

Who the study is looking for

  • Age over 18 years.
  • First diagnosis of ischemic stroke, documented radiologically via CT or MRI scans, corresponding to ICD-9-CM codes 433 and 434 .
  • Presence of aphasia, as assessed by the Aachener Aphasia Test (AAT), and/or cognitive deficits identified through the Oxford Cognitive Screen (OCS).
  • Availability of an ADSL or higher-speed internet connection at the patient's residence.
  • Ability of the patient and/or caregiver to understand and utilize the telerehabilitation system.
  • Provision of written informed consent.

Age in the registry: 18 years to 90 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
Azienda Ospedaliera Universitaria Integrata Verona - UOC di Neuroriabilitazione
Coordinator of this site? Confirm its status
VeronaItalyRecruiting

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