Functional Neuroanatomy of Emotion Perception, Recognition, Learning, and Memory
2 other identifiers
observational
180
1 country
1
Brief Summary
This study uses magnetic resonance imaging (MRI) to explore the areas of the brain involved in different types of mental processes, in particular, the brain regions involved in perception, recognition, learning, and memory. MRI uses a magnetic field and radio waves to produce images of body tissues and organs. In this study it is also used to measure blood flow in different regions of the brain while the subject is presented auditory or visual stimuli. The subject lies on a table that can slide in and out of the scanner (a narrow cylinder), wearing earplugs to muffle loud noises that occur during the scanning process. Subjects are in the scanner no more than 2 hours. Healthy, right-handed normal volunteers between 20 and 40 years of age who have at least a high school education may be eligible for this study. While undergoing MRI, participants are presented visual stimuli (pictures or geometric shapes on a projection screen) or auditory stimuli (tones played through a set of headphones). Unpleasant stimuli such as loud noise, electric shocks, heat, or tactile stimuli are administered occasionally. The intensity of these stimuli is similar to those experienced in practice sessions before the scanning. Participants receive between 30 and 60 visual or auditory stimuli during the scanning session, and each stimulus lasts about 1 second. In some studies participants are asked to move a joystick that controls a rating bar presented on a projection screen to indicate when they expect to receive these stimuli and how sure they are that they will occur. Heart rate, respiration rate, and sweat gland activity are monitored during the MRI sessions, using electrodes placed on the fingers to measure heart rate and sweat gland activity and a sensor strapped around the chest to measure respiration. Subjects are in the scanner no more than 2 hours. Following the experiment, subjects may be asked questions about their experiences during the study.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Apr 2007
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
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 5, 2007
CompletedFirst Submitted
Initial submission to the registry
April 7, 2007
CompletedFirst Posted
Study publicly available on registry
April 10, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 31, 2009
CompletedStudy Completion
Last participant's last visit for all outcomes
August 31, 2009
CompletedJuly 2, 2017
June 8, 2009
2.4 years
April 7, 2007
June 30, 2017
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- Normal right-handed volunteers with at least a high school education, age 20 to 40 years, will be recruited to participate in this study.
You may not qualify if:
- Subjects will be excluded if they have evidence of or a history of learning disability, psychiatric condition, head trauma, seizures or other neurological condition, alcoholism or substance abuse, hypertension, or cardiovascular disease. We will also exclude subjects with vision and/or hearing problems severe enough to interfere with testing. Lab work will be limited to a urine pregnancy test for females. Females with a positive pregnancy test will be excluded from neuroimaging studies. All subjects will be questioned prior to MRI scanning for possible occupational exposure to metal slivers or shavings, which may have become accidentally lodged in the tissues of the head or neck. Those whose history is suggestive of such a problem will be excluded. Subjects with surgical clips or shrapnel in or near the brain or blood vessels, subjects with cochlear implants, subjects with any metallic body in the eye or CNS, and subjects with any form of implant wire or metal device which may concentrate radiofrequency fields will be excluded because of possible risks during MRI scanning.
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)
Baumgartner U, Magerl W, Klein T, Hopf HC, Treede RD. Neurogenic hyperalgesia versus painful hypoalgesia: two distinct mechanisms of neuropathic pain. Pain. 2002 Mar;96(1-2):141-51. doi: 10.1016/s0304-3959(01)00438-9.
PMID: 11932070BACKGROUNDBechara A, Tranel D, Damasio H, Adolphs R, Rockland C, Damasio AR. Double dissociation of conditioning and declarative knowledge relative to the amygdala and hippocampus in humans. Science. 1995 Aug 25;269(5227):1115-8. doi: 10.1126/science.7652558.
PMID: 7652558BACKGROUNDAndrew D, Greenspan JD. Peripheral coding of tonic mechanical cutaneous pain: comparison of nociceptor activity in rat and human psychophysics. J Neurophysiol. 1999 Nov;82(5):2641-8. doi: 10.1152/jn.1999.82.5.2641.
PMID: 10561433BACKGROUND
Study Design
- Study Type
- observational
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- NIH
Study Record Dates
First Submitted
April 7, 2007
First Posted
April 10, 2007
Study Start
April 5, 2007
Primary Completion
August 31, 2009
Study Completion
August 31, 2009
Last Updated
July 2, 2017
Record last verified: 2009-06-08