Stroke Clinical Trial
— RehAttOfficial title:
Assessment and Training Visio Spatial Neglect in a Virtual Reality Environment
Verified date | October 2014 |
Source | Umeå University |
Contact | n/a |
Is FDA regulated | No |
Health authority | Sweden: Regional Ethical Review Board |
Study type | Interventional |
There is a lack of effective rehabilitation methods for visio-spatial neglect (VSN). By
using virtual technology, a new method (virtual reality, VR method) has been created which
focuses on stimulating attention networks: top down scanning training in a 3D game, combined
with intense visual, audio and tactile bottom-up stimulation, also including visuo-motor
training.
Objective. To evaluate clinical and functional improvement in stroke patients with VSN, as
well as before and after training with the new VR method Method:- An intense visio spatial
scanning training, enhanced by directed visual, audio and tactile stimulation cues and
feedback, also including visio-motor activation was designed in a VR game. The in-house
developed software was based on the Tetris game. The VR method consists of an interactive 3D
environment: a desktop computer, a monitor, 3D glasses and a force feedback interface. 15
patients with chronic (>6 months) visio spatial neglect was included due to right-sided
ischemia. A VR neglect test battery including a Posner task were repeated three times during
a 5 weeks baseline before the training started (to establish the chronic state) and again
after 15 hours training (3x1 h for 5 weeks). Evaluation of a new method for training
attention after stroke causing visio spatial neglect.
The method has been designed for home rehabilitation and is well suited for a tele-medicine
approach. It was built with standard components and is easy to manufacture at a low cost.
The idea is to give access to effective training, to make it available at the stroke unit
with the possibility for the patient to loan it it at discharge for home rehabilitation. The
concept of an all in one, easy-to-use device for testing, training and outcome evaluation
should be beneficial These preliminare results has been promising and indicates that the
RehAtt™ method could become an further developed into an effective and stimulating
intervention tool that would lower rehabilitation costs and reduce tiresome travelling to
hospitals for training.
Status | Completed |
Enrollment | 15 |
Est. completion date | June 2012 |
Est. primary completion date | June 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 60 Years to 85 Years |
Eligibility |
Inclusion Criteria: - Neglect > 6 months and after regular rehabilitation Stroke due to right sided ischemic infarcts Exclusion Criteria: - Severe visual impairment, severe medical illness, severe depression or cognitive dysfunction (MMSE = 23 points). |
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Sweden | Department of Clinical Neuroscience | Umea |
Lead Sponsor | Collaborator |
---|---|
Umeå University |
Sweden,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Neglect assessment clinical and behavioural | Change in score in; Star cancellation test, Line Bisection, Baking tray task, Posner task, Extinction, Catherine Bergego scale (CBS) | within 1 week after intervention | No |
Secondary | Catherine Bergego scale | Change in score in a scale for spatial attention in daily life activities, self report from patient and relative | 6 month follow up | No |
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