RehAtt: Assessment and Training Visio Spatial Neglect in a Virtual Reality Environment

Sponsor
Umeå University (Other)
Overall Status
Completed
CT.gov ID
NCT02258789
Collaborator
(none)
15
1
1
21
0.7

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: VR-method
N/A

Detailed Description

A VR environment was used training (RehAtt) of post-stroke patients with neglect. Patients played the VR games three times a week for five weeks, totally 15 hours.

A neglect test battery five neglect tests was repeated three times during a five week baseline to estabish a chronic state and reduce the test by test learning effect, then again after the 5 weeks training period. The main outcome results were thereafter obtained by comparing the 5 neglect tests: Star cancellation test, Baking Tray Task, Line Bisection,, Extinction and Posner task - unified index by SPSS Repeated Measurement ANOVA from the 3 baseline visits to the results after intervention. The Catherine Bergego neglect scale was used to assess activities in daily life before and after intervention as well as after six months.

Patients were included if they had a neglect that had persisted for more than six months after a right sided ishemic stroke.

Neglect was diagnosed if one or more of the four neglect subtests of the VR test battery was below cut off (See below and Appendix for details).

The exclusion criteria were severe visual impairment, severe medical illness, severe depression or cognitive dysfunction (MMSE ≤ 23 points). All patients received oral and written information with an informed and signed consent. The Umeå university ethics review board (IRB) approved the study (2010-266-31M).

The hardware consists of a standard PC, a video graphics card, a sound card, headphones and a separate numeric keyboard to measure behavioural responses. In the VR test part, we used a 19" CRT monitor and shutter glasses for stereoscopic vision. A 27" monitor and 3D vision glasses (Nvidia, Santa Clara, CA, USA) replaced them in the VR game part. A robotic pen (Phantom omni haptic device, Sensable technologies, Wilmington, USA) was used as a pointer using the right hand for assessment activities and the paretic left hand when playing the VR game for intervention.

Study Design

Study Type:
Interventional
Actual Enrollment :
15 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Assessment and Training Visio Spatial Neglect in a Virtual Reality Environment
Study Start Date :
Sep 1, 2010
Actual Primary Completion Date :
Jun 1, 2012
Actual Study Completion Date :
Jun 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: intervention - control

15 hours ( 3 times a week in 5 weeks) intense visio spatial scanning training Virtual Reality-method

Other: VR-method
Neglect rehabilitation by intense scanning training and multi sensory stimuli using Virtual Reality
Other Names:
  • RehAtt
  • Outcome Measures

    Primary Outcome Measures

    1. Neglect assessment clinical and behavioural [within 1 week after intervention]

      Change in score in; Star cancellation test, Line Bisection, Baking tray task, Posner task, Extinction, Catherine Bergego scale (CBS)

    Secondary Outcome Measures

    1. Catherine Bergego scale [6 month follow up]

      Change in score in a scale for spatial attention in daily life activities, self report from patient and relative

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    60 Years to 85 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of Clinical Neuroscience Umea Sweden 903 21

    Sponsors and Collaborators

    • Umeå University

    Investigators

    • Principal Investigator: Helena Fordell, MD,, Department of Pharmacology and Clinical Neuroscience Umea University, Sweden

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Umeå University
    ClinicalTrials.gov Identifier:
    NCT02258789
    Other Study ID Numbers:
    • UmeaU ClinNeuro HF Neglect
    • UMU-2010-266-31M
    First Posted:
    Oct 7, 2014
    Last Update Posted:
    Oct 7, 2014
    Last Verified:
    Oct 1, 2014
    Keywords provided by Umeå University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 7, 2014