About this trial
The study aims to explore the patients' perspective on usability and feasibility of the RehAtt™ mixed-reality system during upper limb, gait and balance function rehabilitation.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
first ischaemic or hemorrhagic stroke,
one-sided hemiparesis,
adequate cognitive abilities.
Disqualifiers
severe cognitive impairment,
aphasia,
known presence of an epileptic seizure in the last year,
other orthopaedic and neurological diseases affecting sensory or motor functions,
Trial design
Single group
Treatments tested in this trial
RehAtt
DeviceEach patient received the RehAtt intervention.
Treatment groups
Trial outcomes
Primary outcomes
Semi-structured interview
The interview was based on a questionnaire that included rating-scale-based questions on mixed-reality therapy meeting the patient's needs, frustration during the exercise, ease of use, difficulties encountered, motivational aspect, likability and usefulness of each exercise, and open-ended questions on motivation, overall view of the mixed-reality system and possible unwanted effects.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.