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Taking people in ItalyNo phase

Tests home-based rehabilitation for stroke survivors using a remote device

Compares home telerehabilitation with clinic rehabilitation in adults with stroke aftereffects.

Plain-language title generated from the registry record
Registry title: Effectiveness of a Home-Based Rehabilitation Program in Stroke Survivors Using the Euleria Home® Device

Key facts

Where
Verona, ItalySee 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 90 years old?

Source: NCT06968923, who can take part

Where in Italy

  • Azienda Ospedaliera Universitaria Integrata Verona - UOC di NeuroriabilitazioneVerona, 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?
Print a page for my doctor

Trial details

Who runs it
Universita di Verona
Trial code
NCT06968923
Record updated
13 May 2025
Original description
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.Read full original descriptionShow less

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

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.

Inclusion: 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.

Exclusion: 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.

ClinicalTrials.gov NCT06968923