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Usability study - Is therapy with the VITA system possible with early stroke patients?

Usability study - Is therapy with the VITA system possible with early stroke patients? - MVITA

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00029962
Enrollment
20
Registered
2022-08-19
Start date
2022-10-08
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

I60-I69

Interventions

Group 1: In addition to the existing physiotherapeutic standard care, usual mobilizing and activating exercises for hemiplegia after stroke are to be performed within the framework of a VR application

Sponsors

Deutsches Zentrum für Luft- und Raumfahrt (DLR)Institut für Robotik und MechatronikPerzeption und Kognition
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: i. Age at least 18 years ii. Diagnosis of acute stroke iii. National Institute of Health Stroke Scale (NIHSS) (subscale to quantify the severity of stroke symptoms of upper extremity motor function, 0-4): NIHSS score of motor function: = 1. iv. existing capability of understanding or capacity to consent with subsequent informed consent.

Exclusion criteria

Exclusion criteria: i. limited ability to be mobilized (e.g., bed rest). ii. impaired general health condition affecting participation in the study; this will be queried from the medical ward staff (e.g., unstable cardiovascular condition) iii. Negative experiences with VR use (virtual reality or simulator sickness). iv. known secondary diagnoses or conditions that interfere with participation in the study (for example, the following): - Epilepsy - Vestibular disease - Visual impairments (e.g., neglect, hemianopsia) - Psychiatric conditions that could impact usability (e.g., hallucinations, delirium) - lack of understanding of instructions (e.g., aphasia, language barrier) - musculo-skeletal limitations of the upper extremities - hemicraniectomy - existing pregnancy

Design outcomes

Primary

MeasureTime frame
System Usability Scale

Secondary

MeasureTime frame
meCUE 2.0 score - module III + IV; Simulator-Sickness-Questionnaire; Effectiveness of the VITA system: proportion of patients who were able to complete a full application to proportion of total patients with acute stroke (in %); Efficiency of use of the VITA system: proportion of time spent on individual process substeps in relation to total application time (in %)

Countries

Germany

Contacts

Public ContactJürgen Fröhlich

Universitätsmedizin Mainz

juergen.froehlich@unimedizin-mainz.de06131-17-2822

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026