Characterizing Psychological Consequences of Childhood Trauma

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00209105
Recruitment Status : Completed
First Posted : September 21, 2005
Last Update Posted : November 13, 2013
National Institute of Mental Health (NIMH)
Information provided by (Responsible Party):
Becky Kinkead, PhD, Emory University

September 13, 2005
September 21, 2005
November 13, 2013
January 2005
December 2009   (Final data collection date for primary outcome measure)
Pathophysiological pathways (e.g., blood chemicals, physiological measures, brain images, behavioral measures), as assessed by diagnostic tests [ Time Frame: Measured at Day 2.5 ]
Diagnostic tests are used to identify pathophysiological pathways. Outcome measures: blood chemicals, physiological measures, brain images, behavioral measures (startle).
Complete list of historical versions of study NCT00209105 on Archive Site
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Characterizing Psychological Consequences of Childhood Trauma
Emory Conte Center for the Neuroscience of Mental Disorders: Psychobiology of Childhood Trauma
This study will characterize the mental health consequences of early-life trauma.

This primary goal of this Center is to characterize the neurobiological consequences of early-life trauma. The Center comprises 6 projects that include human subjects. Human subjects are recruited through Project 6.

Project 2: Psychoimmunology (PI A.H. Miller) Project 4: A Model of Learned Safety(PI: M. Davis) Project 6: Clinical Psychobiology(PI: C. Heim) Project 7: Children of Depressed Mothers(PI: Z. Stowe) Project 8: Functional Brain Imaging (PIs: H.S. Mayberg, G. Berns) Project 9: Structural & Anatomical Connectivity Studies (PI: C.Kilts, X. Hu).

Project 2: The study seeks to examine the impact of psychosocial stress on neuroendocrine and immune signaling pathways of adult men and women with and without major depression who have experienced serious trauma (abuse, loss) during development. Serial blood samples will be collected at baseline and after an acute speech/math stressor (see Project 6). Assessments include IL-1alpha, and beta, IL-6, TNF alpha as well as DNS binding of relevant neuroendocrine-immune transcription factors, i.e. GR, CREB, and NFkB.

Project 4: This study uses a model of that allows for the independent evaluation of excitation and inhibition of fear-conditioning measured with the acoustic startle reflex. In addition, a dark-enhanced startle paradigm will be used that tests for anxiety. The effects of early-life stress will be evaluated in humans with and without major depressive disorder.

Project 6: This study assesses neuroendocrine and autonomic responses to stress and pharmacological challenge in subjects with and without major depression who have or have nor experienced early life stress. We seek to identify causes of variability in neuroendocrine-autonomic outcome after early life stress. To achieve this principle aim, we study the role of moderating and mediating factors including gender, genotype, type/timing of childhood trauma, as well as the role of adulthood trauma, comorbidity and cognitive dysfunction. The projects serves as a human subjects core for the other projects.

Project 7: This project characterizes effects of maternal depression on offspring in a longitudinal study. Women with and without depression will be prospectively followed through pregnancy and the first 6 months post-partum. Maternal stress and psychopathology, pregnancy and birth complications, medications and infants' physiological and behavioral stress responses will be assessed.

Project 8: This study uses PET and fMRI to characterize the impact of early-life stress on functional neural pathways mediating mood reactivity, self reference and reward-processing in patients with major depression. Cortical-limbic-striatal changes in cases with early stress but no psychopathology that define vulnerability to depression are also identified.

Project 9: This Project uses data obtained in Project 8 as well as diffusion tensor imaging to define the influence of early-life trauma on brain anatomical and functional connectivity.

Observational Model: Case-Only
Time Perspective: Prospective
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Probability Sample
This study will include participants who have experienced early-life trauma.
Major Depressive Disorder
  • Drug: DEX-CRF stimulation test
    1 ug/kg body weight of CRF for determining hpa response post dexamethasone ingestion
  • Behavioral: Psychosocial stress induction
    Laboratory stress induction, no drug administration
  • Procedure: Brain imaging of sad mood , self-reference, reward
    Brain imaging
  • Behavioral: Acoustic startle
    No drugs involved
Participants who have experienced early-life trauma will undergo a series of diagnostic tests.
  • Drug: DEX-CRF stimulation test
  • Behavioral: Psychosocial stress induction
  • Procedure: Brain imaging of sad mood , self-reference, reward
  • Behavioral: Acoustic startle
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*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
March 2011
December 2009   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • For participants assigned to the MDD groups: current DSM-IV diagnosis of MDD
  • For participants assigned to the early-life stress group: repeated (once per month or more for at least year) sexual or physical abuse before the age of 13 years by a perpetrator at least 5 years older at the time
  • For female participants: regular menstrual cycle and assessment in the early follicular phase as verified by sex steroid measures

Exclusion Criteria:

  • Meets DSM-IV criteria for a gender identity disorder
  • For all participants assigned to non-MDD groups: DSM-IV diagnosis of current MDD
  • For all participants assigned to the group without early-life stress: major stress experiences before the age of 12 years, such as separation from parents, neglect, parental loss, accidents, severe illness, or natural disaster
  • Significant medical illness, such as gastrointestinal, neurological, hormonal, heart, lung, kidney, liver, immunological or hematological disease, organic brain disease, or cancer as determined by history, physical examination, ECG, and laboratory tests
  • Pregnant or breastfeeding
  • Past or current presence of psychotic symptoms or bipolar disorder
  • Current presence of psychoactive substance abuse/dependency or eating disorders
  • Currently taking hormonal medication
  • Taking psychotropic medication within 4 weeks of study entry
  • General exclusion criteria for PET and fMRI
Sexes Eligible for Study: All
18 Years to 45 Years   (Adult)
Contact information is only displayed when the study is recruiting subjects
United States
P50MH058922 ( U.S. NIH Grant/Contract )
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Becky Kinkead, PhD, Emory University
Emory University
National Institute of Mental Health (NIMH)
Principal Investigator: Becky Kinkead, PhD Emory University SOM - Dept. of Psychiatry and Behavioral Sciences
Emory University
November 2013