Prenatal Drug Exposure: Effects on the Adolescent Brain and Behavior Development

NCT ID: NCT01020669

Last Updated: 2017-07-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

24 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-10-16

Study Completion Date

2011-07-13

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Background:

\- Recent research has suggested that prenatal exposure to drugs may affect specific brain processes, including working memory, stress response, and decision making. However, most of the research on the effects of prenatal drug exposure in humans has been conducted early in life, and very little is known about effects of prenatal drug exposure during the crucial brain development period that takes place during puberty and adolescence. The biological and psychological changes associated with puberty may increase adolescents' sensitivity to prenatal substance exposure. Researchers are interested in using functional magnetic resonance imaging (fMRI) scans to study brain function and learn more about the effects of prenatal drug exposure on adolescents.

Objectives:

\- To examine the effects of prenatal substance exposure on working memory, decision making, and normal brain activity in adolescents.

Eligibility:

\- Adolescents between 12 and 17 years of age who are enrolled in a larger follow-up study of children exposed to drugs in utero.

Design:

* The study will involve a single outpatient session with two fMRI scans that will test working memory and decision-making processes.
* Participants will have brief medical history, a physical examination, and a urine test for drugs of abuse.
* Participants will then be trained on the working memory and decision-making tasks before having an initial MRI scan to provide a baseline reading.
* The fMRI scans will take 40 to 45 minutes each, and participants will have break in between as needed.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Objective- To use fMRI to compare brain activity at rest and during working memory and decision making tasks in normal children and in children exposed in utero to drugs of abuse.

Study population- All participants will be 12-17 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 working memory task, a decision making task and at rest. Data from participants in the current study will be combined with those from a previous study (NIDA protocol 417) which now reside in our repository protocol, 8002.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Drug Abuse Prenatal Drug Exposure

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Study Time Perspective

OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. Participants must be enrolled in the current UMB longitudinal study protocol.
2. All participants will be between 12 and 17 years old (inclusive).
3. All participants must be able to provide informed assent and have a parent/guardian who can provide informed consent.

Exclusion Criteria

1. Report of a history of significant medical/neurological illness that might interfere with imaging data such as HIV positive status, cerebral vascular accident (CVA), central nervous system (CNS) tumor, head trauma, multiple sclerosis (MS) or other demyelinating diseases, epilepsy, or movement disorders.
2. Metallic devices in the body that preclude MRI scanning, as determined by self and parent (guardian) report.
3. Current use of psychotropic medication that may alter attentional functioning (e.g., Clonidine, antipsychotics, Effexor, stimulants).
4. Currently using respiratory, cardiovascular, anticonvulsant or other medications that might interfere with the mechanisms producing the BOLD signal.
5. Currently abusing street drugs as assessed by history and urine testing.
6. Pregnancy, which will be assessed by history during screening and by urine testing on scan days.
7. Claustrophobia by self and/or parent (guardian) report severe enough to preclude toleration of the scanning environment.
Minimum Eligible Age

13 Years

Maximum Eligible Age

17 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

National Institute on Drug Abuse (NIDA)

NIH

Sponsor Role lead

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University of Maryland at Baltimore/MPRC

Catonsville, Maryland, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

References

Explore related publications, articles, or registry entries linked to this study.

Accornero VH, Morrow CE, Bandstra ES, Johnson AL, Anthony JC. Behavioral outcome of preschoolers exposed prenatally to cocaine: role of maternal behavioral health. J Pediatr Psychol. 2002 Apr-May;27(3):259-69. doi: 10.1093/jpepsy/27.3.259.

Reference Type BACKGROUND
PMID: 11909933 (View on PubMed)

Bandstra ES, Morrow CE, Anthony JC, Accornero VH, Fried PA. Longitudinal investigation of task persistence and sustained attention in children with prenatal cocaine exposure. Neurotoxicol Teratol. 2001 Nov-Dec;23(6):545-59. doi: 10.1016/s0892-0362(01)00181-7.

Reference Type BACKGROUND
PMID: 11792524 (View on PubMed)

Ashtari M, Kumra S, Bhaskar SL, Clarke T, Thaden E, Cervellione KL, Rhinewine J, Kane JM, Adesman A, Milanaik R, Maytal J, Diamond A, Szeszko P, Ardekani BA. Attention-deficit/hyperactivity disorder: a preliminary diffusion tensor imaging study. Biol Psychiatry. 2005 Mar 1;57(5):448-55. doi: 10.1016/j.biopsych.2004.11.047.

Reference Type BACKGROUND
PMID: 15737658 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

10-DA-N455

Identifier Type: -

Identifier Source: secondary_id

999910455

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

MDMA in Borderline Personality Disorder
NCT06683014 RECRUITING PHASE2
Influence of Medication on Functional Connectivity
NCT03612713 COMPLETED EARLY_PHASE1
Neurobiology of Opioid Dependence: 1 - 1
NCT00000192 WITHDRAWN PHASE2
Neurobiology of Opioid Dependence: 3 - 3
NCT00000194 WITHDRAWN PHASE2
Prosocial Effects of MDMA
NCT05948683 COMPLETED EARLY_PHASE1