Home-based rehabilitation program for stroke survivors using Euleria Home® device
Effectiveness of a Home-Based Rehabilitation Program in Stroke Survivors Using the Euleria Home® Device: A Crossover Study.
This study tests whether a home-based rehabilitation program using the Euleria Home® device can help stroke survivors improve their motor, cognitive, and language skills just as well as traditional in-person therapy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 90 (estimated) |
| Ages | 18 Years to 90 Years |
| Sex | All |
| Sponsor | Universita di Verona Academic / other |
| Locations | 1 site (Verona, verona) |
| Trial ID | NCT06968923 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of a multidomain telerehabilitation protocol compared to conventional outpatient rehabilitation for stroke survivors. It focuses on assessing motor, cognitive, and language functions in patients who have experienced a stroke. The study will determine if there are no significant differences in treatment effects between the two approaches, indicating that telerehabilitation is a viable alternative. Participants will receive either in-person treatment or telerehabilitation through the Euleria Home® device.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 who have experienced their first ischemic stroke and have cognitive or language deficits.
Not a fit: Patients with severe cognitive decline or other neurological and orthopedic conditions that interfere with the study may not benefit.
Why it matters
Potential benefit: If successful, this approach could provide stroke survivors with effective rehabilitation options from the comfort of their homes.
How similar studies have performed: Other studies have shown promising results with telerehabilitation approaches, suggesting potential for success in this area.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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 Criteria: * 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.
Where this trial is running
Verona, verona
- Azienda Ospedaliera Universitaria Integrata Verona - UOC di Neuroriabilitazione — Verona, verona, Italy (Recruiting)
Study contacts
- Study coordinator: Valentina Varalta
- Email: valentina.varalta@univr.it
- Phone: 045 8124956
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.