Stroke, cardiovascular disease, CVD Stroke
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The participant must be 18 years or older; Have command of the Dutch language; Time after the stroke is longer than 3 months; Have a Functional Ambulation Category of 3 (ambulator, dependent on supervision), 4 (ambulator, independent level surface only), or 5 (ambulator, independent).Additional criterion for people with a FAC of 5: Gait and/or balance impairments identified by the therapist.
Exclusion criteria
Exclusion criteria: The participant must not have progressive neurological disorders (e.g., Parkinson's disease) and/or orthopaedic problems seriously interfering with gait, balance and/or upper limb functioning; Insufficient physical capacity to comply with the (training) protocol (e.g., frequent faller); Severe cognitive impairments to understand instructions (as observed by the researcher or therapist) ; Severe visual or hearing impairments (after corrective aids) which ensure that Strolll Rehab cannot be used appropriately.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study parameters of the clinical feasibility study to evaluate the feasibility of Strolll Rehab in the clinical pathway are safety, adherence, performance and user experience (i.e., post-stroke individuals and their therapist). The main study parameters of the clinical feasibility study to evaluate the effectiveness of Strolll Rehab are gait, balance, and upper-limb outcome measures from standard clinical tests.The main study parameters for the data quality study are outcome measures of gait, balance and upper-limb functioning derived from AR headsets and various reference systems (i.e., Theia3D and/or stopwatch). | — |
Countries
Netherlands
Contacts
Vrije Universiteit