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Assessment of the Cyberlink Control System for Use by the ALS Patient

 
Study Focus:
The goal of this project is to determine whether this device is a practical and realistic means for ALS patients to operate their computers with only the use of facial, brainwave, and eye movements.
Disease:
Amyotrophic Lateral Sclerosis (ALS), Sporadic ALS, Familial ALS
Study Category:
Device
Study Status:
Closed
Study Results:
New protocol was developed based on preliminary results from this study.
Phase:
Not Applicable
Type:
Observational Study
Funding Source:
MDA/ALS Center of Hope
Study Chair(s)/Principal Investigator(s):
Terry Heiman-Patterson, MD (MDA/ALS Center of Hope)
Clinicaltrials.gov ID:
NCT00718016
NEALS Affiliated?
No
Study Summary:
The goal of this project is to determine whether this device is a practical and realistic means for ALS patients to operate their computers with only the use of facial, brainwave, and eye movements. This study is intended to evaluate both the complexity of the system and the degree to which complications of ALS (such as severity of involuntary movements) may interfere with the use of cyberlink.


# of Subjects:
25
Enrollment Start Date:
12/01/2004
Posting Last Modified Date:
03/01/2013
Date Study Added to alscortium.org:
11/03/2011
Eligibility Criteria
Gender:
Male & Female
Minimum Age:
18
Maximum Age:
75
Min Vital Capacity (% predicted normal):
N/A
Time since Symptom Onset:
Not applicable
Time since Diagnosis:
Not applicable
Can participants use Riluzole?
Yes
Coordinating Center
Contact Information
Christine Barr, RN
cbarr@drexelmed.edu
267-507-2585
MDA/ALS Center of Hope
Philadelphia, Pennsylvania 19104
UNITED STATES
Other Eligibility Criteria:
Inclusion Criteria:

•Those aged 18-75 diagnosed with probable or definite ALS.
Exclusion Criteria:

•Those with decision impairment will not be considered.

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