Using an electronic device for cognitive rehabilitation in stroke patients
Self Treatment with an Electronic Device for Cognitive Rehabilitation in Patients with Subacute Stroke: a Randomized Controlled Trial
This study tests if using an electronic device for self-treatment can help stroke patients improve their attention skills better than regular rehab methods.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 42 (estimated) |
| Ages | 18 Years to 90 Years |
| Sex | All |
| Sponsor | Universita di Verona Academic / other |
| Locations | 2 sites (Verona and 1 other locations) |
| Trial ID | NCT06755437 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of self-treatment with an electronic device for cognitive rehabilitation in patients who have experienced a stroke. Participants will engage in rehabilitation sessions using a computerized device in the morning and perform self-treatment exercises in the afternoon, including both computerized and pencil-and-paper tasks. The goal is to determine if this approach enhances attentional function outcomes compared to standard rehabilitation methods. The study focuses on patients with cognitive deficits following a stroke, aiming to improve their recovery process.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 to 90 who have experienced their first stroke more than 30 days prior and have cognitive deficits such as memory or attention disorders.
Not a fit: Patients with other neurological conditions, pre-existing cognitive decline, or severe visual impairments may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance cognitive rehabilitation outcomes for stroke patients.
How similar studies have performed: While there is ongoing research in computerized rehabilitation for stroke, this specific approach of self-treatment with an electronic device is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Diagnosis of ischemic or hemorrhagic stroke; * Age between 18 and 90 years; * First stroke event; * Time since the stroke greater than 30 days; * Adequate level of comprehension; * Presence of one or more of the following cognitive disorders: Memory disorders; Attention disorders; Executive function disorders * Availability of internet access at the patient's home, necessary for telemedicine procedures. Exclusion Criteria: * Presence of other neurological conditions; * Presence of pre-morbid cognitive decline; * History of psychiatric disorders; * Alcohol and/or drug abuse; * Presence of severe uncorrected visual impairments.
Where this trial is running
Verona and 1 other locations
- Azienda Ospedaliera Universitaria Integrata Verona - UOC di Neuroriabilitazione — Verona, Italy (Completed)
- Azienda Ospedaliera Universitaria Integrata Verona - UOC di Neuroriabilitazione — 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.