Development of Reward Processing in Prenatally Exposed Adolescents and Young Adults
Completed
Conditions studied: Pre-natal Cocaine Exposure, Risk-Taking
In brief
Reward processing will be examined in prenatally exposed emerging adults in a longitudinal design. Participants will be followed for one year to see if neural markers of reward processing prospectively predict risk-taking behavior.
Key facts
- Study ID
- NCT03268759
- Run by
- Yale University
- People needed
- 78
- Starts
- 2017-09-15
- Expected to finish
- 2020-09-14
- Last updated by the study team
- 2021-05-04
Who can join
Age: 18 and older, up to 20. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Ability to provide written informed consent and to comply with all study procedures.
- Healthy emerging adults between 18-20 years of age (the age of the currently followed sample at the time of the proposed start date).
You may not qualify if…
- 1. A serious neurological or endocrine disorder or any medical condition or treatment known to affect the brain. 2. A medical condition that requires treatment with a medication with psychotropic effects.
- Evidence of stroke or space occupying lesions observed on conventional, clinical MR images.
- Any contraindications to MRI scanning (i.e., metal implants, pacemakers, etc.) 5. History of loss of consciousness (LOC) for longer than 30 minutes or LOC with any neurological sequelae.
- DSM-5 criteria for intellectual disability. 7. Current or a history of active neurological or psychiatric disorders, such as psychosis, bipolar illness, major depression, organic brain disease, dementia or DSM-V Axis I Psychiatric Disorder, including current alcohol or substance disorders. Participants will not be excluded for substance or alcohol use, only the presence of substance disorders.
- Current pregnancy. Female participants will be excluded if they report being currently pregnant or present positive for pregnancy after being given a urine test at the time of recruitment or scanning. If they become pregnant during the one-year follow-up duration of the study after the MRI scan is completed, they will remain in the study for the quarterly follow-ups and be referred to pre-natal care if they have not begun such care already.
Where it is running
- Child Study Center — New Haven, Connecticut, United States
Full record on ClinicalTrials.gov
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