Telerehabilitation for Post-stroke Patients
Stroke Sequelae
About this trial
This is an interventional treatment trial for Stroke Sequelae focused on measuring Healthcare organizations, Integrated care delivery systems, Cost-benefit analysis, Stroke, Pharmacoeconomics, Rehabilitation, Telerehabilitation, Healthcare organizations, programs, and delivery of services, Disease management and modeling
Eligibility Criteria
Inclusion Criteria:
- first diagnosis of ischemic brain stroke documented radiologically by brain CT or MRI;
- aphasia documented at the Aachener Aphasia Test (AAT) and/or presence of cognitive deficits documented at the neuropsychological assessment with the Oxford Cognitive Screen (OCS).
- availability of ADSL or higher internet connection at home
- ability of the subject and/or caregiver to understand and use the telerehabilitation system
- signature of informed consent
Exclusion Criteria:
- contemporary participation in other clinical studies;
- cognitive impairment defined as a Montreal Cognitive Assessment (MoCA) score <26;
- bone deformities as a consequence of previous traumatic events in the 4 limbs;
- contractures fixed to the 4 limbs assessed as 4/4 on the modified Ashworth scale (MAS);
- other neurological and orthopaedic diseases interfering with the study.
Particularly vulnerable populations. The following cannot be included in the study:
- patients with judicial interdiction
- patients with supportive administration
- institutionalized patients
Criteria for the ongoing exit from the study
- Relapse of disease during the study period
- Withdrawal of informed consent to participate in the study
- Impossibility to carry out the rehabilitation treatment or the assessments required by the study protocol according to the defined schedule.
Sites / Locations
- Section of Clinical Neurology, Department Neurological, Neuropsychological, Morphological and Movement Sciences, University of Verona, Verona, ItalyRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Telerehabilitation group
Conventional rehabilitation group
Patients in this group will undergo 20 sessions (1 hour a day, 5 days a week for 4 consecutive weeks) of "multidomain" telerehabilitation (motor, speech and/or cognitive) with VRRS, K-Wand and Khymu connected to a workstation (Telecockpit).
The patients assigned to this group will undergo 20 sessions (1 hour a day, 5 days a week for 4 consecutive weeks) of "multidomain" rehabilitation (motor, speech and/or cognitive). It is not possible a priori to precisely define the instruments that will be used during rehabilitation management. The telerehabilitation or conventional treatment methods (type of therapeutic exercise, modality of cognitive stimulation and/or taking care of speech therapy) will be determined for each patient on the basis of the needs emerging from the physiatric examination performed at T0, defined according to the Individual Rehabilitation Project and applied according to each Rehabilitation Program (motor, cognitive and/or speech therapy) periodically updated.