Hemispatial Neglect Clinical Trial
Official title:
Evaluating the Feasibility and Usability of Exergames on Exploring the Hemineglected Space in Stroke Patients With Visuo-spatial Neglect
Verified date | February 2017 |
Source | University of Zurich |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The aim of this study is to evaluate the feasibility and usability of newly developed exergames on exploring the hemineglected space of left neglected stroke patients. Furthermore to understand the experience of living with visuospatial neglect and to explore the users' experiences (patients and clinic staff) with those new exergames.
Status | Completed |
Enrollment | 7 |
Est. completion date | February 2017 |
Est. primary completion date | April 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients with visuo-spatial neglect on the left side resulting from a right hemisphere lesion due to a stroke (as measured by the Catherine Bergego Scale (CBS) - Stroke incident between 15 to 180 days at the time point of study inclusion - In possession of power of judgement regarding to the participation in the study - Ability to sit in a (wheel-)chair with a backrest for 45 minutes maximum - Age =18 years Exclusion Criteria: - Diagnosis of a brain injury other than stroke - Other visuospatial syndromes than neglect (e.g. hemianopsia, Balint-syndrome) - Occurrence of severe apraxia (? 5 points on the Apraxia Screening Tool of TULIA (AST)) (that makes the use of the platform impossible, e.g. not knowing how to use the Novint Falcon haptic device) - Non-controlled medical conditions (chronic pain, drug abuse) - Poor vision (that makes the use of the platform impossible, e.g. not being able to see clearly on a distance of 60-65cm (placement of PC screen)) |
Country | Name | City | State |
---|---|---|---|
Switzerland | Klinik Bethesda | Tschugg | Berne |
Switzerland | Zürcher Höhenklinik Wald | Wald | Zürich |
Lead Sponsor | Collaborator |
---|---|
University of Zurich |
Switzerland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Feasibility of exergames as measured by training diary. | During the intervention (3 weeks). | 3 weeks | |
Secondary | Usability of exergames as measured by questionnaire. | Questionnaire: After termination of the intervention (3 weeks) | 7-8 weeks | |
Secondary | Understanding the experience of living with visuospatial neglect as measured by interviews. | Interview: 4 weeks after termination of the intervention (3 weeks) during follow-up. | 7-8 weeks | |
Secondary | Collecting preliminary data for efficacy as measured by the ZüMAX, the NET and the Eye Tribe Tracker. | Pre-, post- and 4 weeks after training intervention (3 weeks). | 7-8 weeks |
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