An In-home Study of Brain Computer Interfaces
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ClinicalTrials.gov Identifier: NCT01123200 |
Recruitment Status :
Completed
First Posted : May 14, 2010
Results First Posted : March 15, 2017
Last Update Posted : March 15, 2017
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Tracking Information | ||||
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First Submitted Date ICMJE | May 4, 2010 | |||
First Posted Date ICMJE | May 14, 2010 | |||
Results First Submitted Date ICMJE | January 12, 2017 | |||
Results First Posted Date ICMJE | March 15, 2017 | |||
Last Update Posted Date | March 15, 2017 | |||
Study Start Date ICMJE | January 2010 | |||
Actual Primary Completion Date | May 2011 (Final data collection date for primary outcome measure) | |||
Current Primary Outcome Measures ICMJE |
Duration of BCI Usage by Persons With ALS. [ Time Frame: Monthly measurements for a period of up to 18 months. ] Number of months of BCI usage by each participant.
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Original Primary Outcome Measures ICMJE |
Duration of BCI usage by patients with ALS. [ Time Frame: On average, 1 year ] | |||
Change History | ||||
Current Secondary Outcome Measures ICMJE |
Changes in Accuracy of BCI for Controlling Devices and Text [ Time Frame: 6 months, 12 months, 18 months ] Changes in Accuracy Percentage (i.e., cumulative correct selections per month divided by the cumulative number of intended sections per month). Looking for trends over each 6 month period.
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Original Secondary Outcome Measures ICMJE | Not Provided | |||
Current Other Pre-specified Outcome Measures | Not Provided | |||
Original Other Pre-specified Outcome Measures | Not Provided | |||
Descriptive Information | ||||
Brief Title ICMJE | An In-home Study of Brain Computer Interfaces | |||
Official Title ICMJE | An In-home Study of Brain Computer Interfaces | |||
Brief Summary | The investigators are developing a tool to help people who are severely paralyzed. This tool is called a brain-computer interface (BCI). BCIs can connect to computers or other electronic devices. This study allows a person with ALS to communicate, control their wheelchair tilt and perform other tasks using a BCI, thus increasing their independence. |
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Detailed Description | This small-scale study of the feasibility of a BCI to operate the tilt position of a power wheelchair was also designed to determine the conditions and support structures necessary for use of a BCI in the home. In this study, people with Amyotrophic Lateral Sclerosis (ALS) will have a BCI in their home. They will receive training in order to operate and maintain the BCI. The BCI will allow them to access at least one task of primary interest to them. Task may include communication, computer access, control of assistive technology, or control of wheelchair seat position. Data concerning the use of the BCI will be collected throughout the study. Custom installations will be made for each participant to connect to their wheelchair and provide communication options if needed. Each installation is expected to be a unique prototype because of the differing control requirements for the individual wheelchairs in use by the participants. We intended to enroll six participants, but were only able to enroll one. |
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Study Type ICMJE | Interventional | |||
Study Phase ICMJE | Not Applicable | |||
Study Design ICMJE | Allocation: N/A Intervention Model: Single Group Assignment Masking: None (Open Label) Primary Purpose: Supportive Care |
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Condition ICMJE | Amyotrophic Lateral Sclerosis | |||
Intervention ICMJE | Device: Brain Computer Interface for Wheelchair Tilt Control
Patients will be given the BCI for use in-home, as long as they use the BCI at least 10 hours per week and complete monthly performance assessment sessions.
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Study Arms ICMJE | Brain Computer Interface In-Home Use
Intervention: Device: Brain Computer Interface for Wheelchair Tilt Control
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Publications * | Not Provided | |||
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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Recruitment Information | ||||
Recruitment Status ICMJE | Completed | |||
Actual Enrollment ICMJE |
1 | |||
Original Estimated Enrollment ICMJE |
6 | |||
Actual Study Completion Date ICMJE | May 2011 | |||
Actual Primary Completion Date | May 2011 (Final data collection date for primary outcome measure) | |||
Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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Sex/Gender ICMJE |
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Ages ICMJE | 18 Years and older (Adult, Older Adult) | |||
Accepts Healthy Volunteers ICMJE | No | |||
Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | |||
Listed Location Countries ICMJE | United States | |||
Removed Location Countries | ||||
Administrative Information | ||||
NCT Number ICMJE | NCT01123200 | |||
Other Study ID Numbers ICMJE | J0002 | |||
Has Data Monitoring Committee | No | |||
U.S. FDA-regulated Product | Not Provided | |||
IPD Sharing Statement ICMJE | Not Provided | |||
Current Responsible Party | Jane Huggins, PhD, University of Michigan | |||
Original Responsible Party | Jane Huggins, PhD/Research Assistant Professor, University of Michigan | |||
Current Study Sponsor ICMJE | University of Michigan | |||
Original Study Sponsor ICMJE | Same as current | |||
Collaborators ICMJE | Not Provided | |||
Investigators ICMJE |
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PRS Account | University of Michigan | |||
Verification Date | March 2017 | |||
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |