Exposure Clinical Trial
Official title:
Neural Correlates of Risk-Taking in Urban Adolescents
Objective- To use fMRI to compare brain activity at rest and during memory and decision
making tasks in normal children and in children exposed in utero to drugs of abuse.
Study population- All participants will be 14-20 year-olds enrolled in an ongoing
longitudinal follow up study of children exposed to drugs of abuse in utero funded by NIH. A
subgroup of this study cohort will be invited to participate based on added criteria needed
for scanning studies, such as absence of metal in the body, no significant CNS disease, and
ability to tolerate the scanning environment.
Design- Participants will undergo fMRI scans while performing a memory task, a decision
making task and at rest. Data from participants in the current study may be combined with
those from a previous study (NIDA protocol 417) which now reside in our repository protocol,
8002 and NIDA protocol 455.
Outcome measures- The primary outcome measures will be the difference in BOLD fMRI activation
between drug-exposed participants and those without prenatal exposure to drugs of abuse.
Objective- To use fMRI to compare brain activity at rest and during memory and decision
making tasks in normal children and in children exposed in utero to drugs of abuse.
Study population- All participants will be 14-20 year-olds enrolled in an ongoing
longitudinal follow up study of children exposed to drugs of abuse in utero funded by NIH. A
subgroup of this study cohort will be invited to participate based on added criteria needed
for scanning studies, such as absence of metal in the body, no significant CNS disease, and
ability to tolerate the scanning environment.
Design- Participants will undergo fMRI scans while performing a memory task, a decision
making task and at rest. Data from participants in the current study may be combined with
those from a previous study (NIDA protocol 417) which now reside in our repository protocol,
8002 and NIDA protocol 455.
Outcome measures- The primary outcome measures will be the difference in BOLD fMRI activation
between drug-exposed participants and those without prenatal exposure to drugs of abuse.
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