Imaging and Genetic Investigation of Learning and Decision Making
2 other identifiers
observational
78
1 country
1
Brief Summary
Background: \- Previous research has shown that dopamine, a brain chemical, is involved in decision making. Different genes influence how much dopamine people have in their brains and how that affects their behavior. Researchers will study if genes associated with dopamine affect decision making and impulsiveness. All participants will take tests; some will have brain images taken. Researchers will study the test responses and images; they will look for how differences in these genes affect different types of decision making. Objectives: \- To see if genes involved in a brain chemical, dopamine, are related to impulsiveness on behavioral tests. Eligibility: \- Healthy adults ages 18 to 55. Design:
- Participants will be screened with a medical history and physical exam.
- All participants in this study will have at least 1 outpatient visit to the NIH Clinical Center. Each visit will last 2 4 hours. At the first visit:
- A blood sample will be taken only from participants that have not been previously enrolled in 95-M-0150
- Participants will be given tests of their memory, attention, concentration, and thinking.
- Some participants will have a second visit. It will be scheduled as soon as possible after the first. At the second visit:
- Participants will have an MRI (magnetic resonance imaging). They will have to lie in a scanner for up to 2 hours. The MRI uses magnets, radio waves, and computers to produce detailed pictures of the brain.
- Participants will repeat the tests from the first visit. Some will be done during the MRI.
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 Feb 2014
Longer than P75 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
September 21, 2013
CompletedFirst Posted
Study publicly available on registry
September 25, 2013
CompletedStudy Start
First participant enrolled
February 11, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 10, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
March 5, 2020
CompletedJanuary 24, 2022
January 1, 2022
4 years
September 21, 2013
January 21, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Outcome measures include performance in the behavioral tasks, effects in the magnetic resonance imaging data, and the genotype of individual participants.
Outcome measures include performance in the behavioral tasks, effects in the magnetic resonance imaging data, and the genotype of individual participants.
ongoing
Study Arms (1)
Healthy Adults
Healthy adults healthy adults - male and female
Eligibility Criteria
Healthy Volunteers
You may qualify if:
- Subjects will be eligible for this study if they:
- are between 18 and 55 years of age
- are in good physical health
- speak English well enough to understand task instructions clearly
You may not qualify if:
- Subjects will not be eligible for this study if they:
- have a major medical (e.g. heart disease), neurological (e.g. stroke) or psychiatric (e.g. bipolar disorder) illness
- have a vision and/or hearing problem that interferes with testing
- currently use any psychotropic medication, antidepressants, steroids or opiates
- currently use alcohol in excess of 14 drinks/week for males or 7 drinks/week for females.
- have a lifetime history of or currently have alcohol or substance use or dependence (excluding nicotine) that requires independent, concurrent treatment intervention (such as, antabuse or opiate treatment). This does not include self-help group treatment/intervention.
- cannot understand the consent and procedures or cannot consent themselves to the study
- Smoke more than a half pack of cigarettes a day
- NIMH employees and staff and their immediate family members will be excluded from the study per NIMH policy.
- Female subjects who are pregnant or have a positive pregnancy test 24 hours prior to an experiment 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. 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 from MRI scanning experiments because of possible risks during MRI scanning. Those whose history is suggestive of such a problem will also be excluded from the MRI portion of the experiments. They may still participate in the behavioral experiments.
- Subjects unable to lie flat on their back for up to 2 hours or who are uncomfortable in small close spaces (have claustrophobia) will not be eligible to participate in MRI scans.
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 Links
Study Officials
- PRINCIPAL INVESTIGATOR
Bruno B Averbeck, Ph.D.
National Institute of Mental Health (NIMH)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- NIH
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 21, 2013
First Posted
September 25, 2013
Study Start
February 11, 2014
Primary Completion
February 10, 2018
Study Completion
March 5, 2020
Last Updated
January 24, 2022
Record last verified: 2022-01