Brain Computer Interface Control of a Robotic Device
1 other identifier
observational
23
1 country
1
Brief Summary
Noninvasive Brain-Computer Interfaces (BCIs) have been used to control a number of virtual and physical objects through the voluntary modulation of brain rhythms. Current issues with noninvasive BCIs include exhausting motor imagery tasks and long training times required to achieve competent control. The investigators will address these issues within this protocol, examining new approaches to reduce the effort required by subjects to control a physical object in the task. The PI's hypothesis is: Control of a physical robotic device will increase the performance of subjects in BCI tasks that are analogous to virtual tasks due to greater engagement with a physical output.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Mar 2014
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 18, 2014
CompletedFirst Posted
Study publicly available on registry
February 24, 2014
CompletedStudy Start
First participant enrolled
March 1, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 13, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
March 13, 2016
CompletedJanuary 18, 2018
January 1, 2018
2 years
February 18, 2014
January 16, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Percent of trials correct within each session of Brain Computer Interface experiments.
Accuracy and performance metrics of Brain-Computer Interface tasks over time. This will include the percent of trials correct, percent of trials completed, and time to completion within each session. Combining these metrics, we will examine subject learning over sessions with regression. Exact time frame of sessions will be determined by subject and equipment availability.
Session 1 through 10, within an average of 5 weeks. Each session separated by at least 24 hours.
Study Arms (1)
Healthy Subjects
Noninvasive Brain Computer Interface Control
Eligibility Criteria
Healthy subjects, primarily from individuals on the University of Minnesota Campus and Minneapolis area
You may qualify if:
- Subjects for this study will be healthy, English speaking adult volunteers (18-64 years old).
You may not qualify if:
- History of neurological deficit or traumatic brain injury.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Nils Hasselmo Hall at the University of Minnesota - Twin Cities Campus
Minneapolis, Minnesota, 55455, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Bin He, PhD
University of Minnesota
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 18, 2014
First Posted
February 24, 2014
Study Start
March 1, 2014
Primary Completion
March 13, 2016
Study Completion
March 13, 2016
Last Updated
January 18, 2018
Record last verified: 2018-01