Use of Transcranial Magnetic Stimulation (TMS) and Magnetic Resonance Imaging (MRI) to Study Visual Attention
Transcranial Magnetic Stimulation Studies of Visual Attention
2 other identifiers
observational
30
1 country
1
Brief Summary
The purpose of this study is to learn more about how the brain allows people to focus on important objects and filter out unimportant ones when looking at visual images. Our senses provide us with a vast amount of information at any given moment in time. For example, visual scenes contain many different objects that cannot be processed simultaneously because of the limited processing capacity of the brain's visual system. Evidence suggests that a a network of brain regions selects relevant information and filters out irrelevant information when people view cluttered visual scenes. This study will use transcranial magnetic stimulation (TMS) and functional magnetic resonance imaging (fMRI) to determine how the different brain regions involved in attentional control and filtering interact. Participants in this study will undergo computer tests, an MRI scan, and TMS. During the MRI, participants will look at pictures and count objects appearing on a screen. During the TMS, participants will perform a computer test. Participants' ability to pay attention will be tested with and without TMS. Participants may be asked to return for additional tests in the future....
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 Sep 2000
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
Study Start
First participant enrolled
September 14, 2000
CompletedFirst Submitted
Initial submission to the registry
September 16, 2000
CompletedFirst Posted
Study publicly available on registry
September 18, 2000
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2002
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2002
CompletedJuly 2, 2017
June 8, 2009
1.5 years
September 16, 2000
June 30, 2017
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- All subjects will be healthy, right-handed volunteers between the ages of 20 and 65.
- Subjects must have normal or corrected-to-normal vision.
You may not qualify if:
- Pregnant women will be excluded.
- Subjects with a personal or family history of seizures will be excluded.
- Subjects with a history of neurologic disease, ocular foreign body, increased intracranial pressure, open head injury or significant closed head injury will be excluded.
- Subjects with cochlear implants, implanted brain stimulators, aneurysm clips or other metal in the head (except mouth) will be excluded.
- Subjects taking tricyclic anti-depressants, neuroleptic agents or other drugs that lower the seizure threshold will be excluded.
- Subjects with a history of illicit drug use or who are abusing or withdrawing from alcohol abuse will be excluded.
- Subjects with a history of a major psychiatric disorder will be excluded.
- Subjects with implanted medication pumps, pacemakers, intracardiac lines or significant heart disease will be excluded.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, 20892, United States
Related Publications (3)
Ashbridge E, Walsh V, Cowey A. Temporal aspects of visual search studied by transcranial magnetic stimulation. Neuropsychologia. 1997 Aug;35(8):1121-31. doi: 10.1016/s0028-3932(97)00003-1.
PMID: 9256377BACKGROUNDAmassian VE, Cracco RQ, Maccabee PJ, Cracco JB, Rudell AP, Eberle L. Transcranial magnetic stimulation in study of the visual pathway. J Clin Neurophysiol. 1998 Jul;15(4):288-304. doi: 10.1097/00004691-199807000-00002.
PMID: 9736464BACKGROUNDChen R, Gerloff C, Classen J, Wassermann EM, Hallett M, Cohen LG. Safety of different inter-train intervals for repetitive transcranial magnetic stimulation and recommendations for safe ranges of stimulation parameters. Electroencephalogr Clin Neurophysiol. 1997 Dec;105(6):415-21. doi: 10.1016/s0924-980x(97)00036-2.
PMID: 9448642BACKGROUND
Study Design
- Study Type
- observational
- Sponsor Type
- NIH
Study Record Dates
First Submitted
September 16, 2000
First Posted
September 18, 2000
Study Start
September 14, 2000
Primary Completion
April 1, 2002
Study Completion
April 1, 2002
Last Updated
July 2, 2017
Record last verified: 2009-06-08