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The Psychobiology of Childhood Temperament
This study is currently recruiting participants.
Verified August 2011 by National Institutes of Health Clinical Center (CC)

First Received on May 12, 2003.   Last Updated on December 24, 2011   History of Changes
Sponsor: National Institute of Mental Health (NIMH)
Information provided by: National Institutes of Health Clinical Center (CC)
ClinicalTrials.gov Identifier: NCT00060775
  Purpose

The purpose of this study is to use brain imaging technology to examine brain changes that occur in children when they are exposed to various kinds of emotional tasks and to determine if these changes are related to the child's temperament.

Studies suggest that the risk for developing mood and anxiety disorders in preschool children may be linked to differences in temperament. The relationship between temperament and risk or resilience may reflect the influences of brain activity on behavior at different stages of childhood development. Behavioral inhibition and mood or anxiety disorders have been linked to disturbances in the circuitry of several areas in the brain. However, the involvement of this circuitry in temperament remains unclear. This study will use functional magnetic resonance imaging (fMRI) to examine the function of different parts of the brain in children who have previously undergone temperament studies and have had their temperaments classified.

This study will comprise three clinic visits. At Visit 1, children and their parents will meet with study staff individually and together for psychiatric interviews. Children will undergo a physical examination, medical history, a urine drug test, and practice in an fMRI simulator. Saliva samples will be collected from the children and tests will be given to assess stage of puberty, temperament, intelligence, feelings, experiences, and behavior. Other visits include fMRI scans of the brain and other tasks.


Condition
Mood Disorders
Anxiety Disorders
Adolescents

Study Type: Observational
Official Title: The Psychobiology of Temperament: An fMRI Study

Resource links provided by NLM:


Further study details as provided by National Institutes of Health Clinical Center (CC):

Estimated Enrollment: 980
Study Start Date: May 2003
Detailed Description:

Recent research delineates developmental pathways to mood and anxiety disorders. Among preschool children, prospective and family-based studies suggest that early risk and resilience may be linked to individual differences in temperament or other behavioral characteristics such as risk-intolerance/risk-seeking. The proposal uses fMRI to examine PFC, cingulate cortex, amygdala, and striatal function as well as resting state, in two groups of individuals, (1) temperamentally classified, i.e., individuals previously classified with a state-of-the-art temperament battery and followed prospectively into early adulthood, and (2) classified by patterns of risk behavior and anxiety trait, i.e., individuals classified by level of trait anxiety and propensity for risk-taking behavior.

A total of 980 children will be studied as adolescents and young adults (7-25 years old). The selection of participants for the temperament part of the study will be based on features that were identified during assessments at UMD in the distant past, when the participants were infants and toddlers. Minors can continue to participate after they become adults, and will be re-consented at their first visit after reaching age 18 with the adult volunteer consent form. The pool of participants for the risk behavior part of the study are children, adolescents and young adults recruited from both the community and a cohort of children and adolescents followed at the University of Maryland College Park. Assessments will include psychiatric, behavioral, and neuropsychological batteries. The protocol uses fMRI paradigms previously developed for studies of adolescents or targeting specific processes such as attention, learning and conditioning, social information, motivation, or perception.

The temperament part of the study tests three hypotheses related to inhibited temperament. First, behaviorally inhibited adolescents are hypothesized to exhibit enhanced amygdala activation when exposed to mild threats in the form of facial emotion displays. Second, behaviorally inhibited adolescents are hypothesized to exhibit reduced activation of the PFC and cingulate while attending to emotion vs. physical features present in facial threats. Third, exuberant adolescents are hypothesized to exhibit enhanced activation of striatum and inferior PFC during the presentation of reward stimuli.

For the risk/anxiety part of the study, an additional set of hypotheses related to trait anxiety and risk-taking will be tested. First, anxious adolescents/young adults will activate striatal regions in response to reward more strongly than non-anxious adolescents/young adults. Second, risk-takers will also activate striatal regions in response to reward more strongly than non-risk taking adolescents. Third, we expect an interaction between risk-taking and anxious factors.

Finally, participants will be asked to come back and repeat scanning studies to (1) evaluate the stability of the findings, (2) assess developmental changes, or (3) test additional paradigms.

  Eligibility

Ages Eligible for Study:   7 Years to 25 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria
  • INCLUSION CRITERIA:

Age: 7-25

Consent: Can give consent/assent.

IQ: All subjects will have IQ greater than 70.

Psychopathology: All subjects will be free of lifetime history of psychosis and pervasive developmental disorder.

EXCLUSION CRITERIA:

Any chronic or acute medical condition severe enough to interfere with task performance or completion of questionnaires.

Any medical condition that increases risk for MRI (e.g. pacemaker, metallic foreign body in eye, dental braces).

Any current axis I psychiatric disorder necessitating acute treatment.

Claustrophobia

Pregnancy

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00060775

Contacts
Contact: Patient Recruitment and Public Liaison Office (800) 411-1222 prpl@mail.cc.nih.gov
Contact: TTY 1-866-411-1010

Locations
United States, Maryland
National Institutes of Health Clinical Center, 9000 Rockville Pike Recruiting
Bethesda, Maryland, United States, 20892
Sub-Investigator: Patient Recruitment and Public Liaison Office (PRPL) For more information at the NIH Clinical Center contact            
University of Maryland, College Park Recruiting
College Park, Maryland, United States
Sponsors and Collaborators
  More Information

Additional Information:
Publications:
ClinicalTrials.gov Identifier: NCT00060775     History of Changes
Other Study ID Numbers: 030186, 03-M-0186
Study First Received: May 12, 2003
Last Updated: December 24, 2011
Health Authority: United States: Federal Government

Keywords provided by National Institutes of Health Clinical Center (CC):
Magnetic Resonance Imaging
fMRI
Emotion
Children
Adolescence
Affective Neuroscience
Neuroimaging
Behavioral Inhibition
Depression
Anxiety
Normal Volunteers
Healthy Volunteer
HV

Additional relevant MeSH terms:
Anxiety Disorders
Mood Disorders
Mental Disorders

ClinicalTrials.gov processed this record on February 09, 2012