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Clinical Trials/NCT01129752
NCT01129752CompletedNot Applicable

The Neural Correlates of Mood and Cognitive Bias in a Population at Risk for Depression: Maternal Cognitive and Emotional Functioning

Stanford University2 sites in 1 country240 target enrollmentStarted: February 2004Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
240
Locations
2
Primary Endpoint
Onset of depression

Study Overview

Brief Summary

The purpose of this study is to investigate risk factors associated with depression and how such factors might be transmitted cross-generationally. The investigators are conducting an integrative assessment of emotion regulation and stress reactivity in a group of mothers with and without a history of depression and their daughters.

Detailed Description

The purpose of this study is to investigate risk factors associated with depression and how such factors might be transmitted cross-generationally. We are conducting an integrative assessment of emotion regulation and stress reactivity in a group of mothers with and without a history of depression and their daughters. We use a range of methodologies to evaluate these processes, including self-report measures, information-processing performance, HPA-axis functioning and reactivity, and neural responses to emotional stimuli following exposure to stressful experiences.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Ages
9 Years to 15 Years (Child)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Eligible mothers must read and speak English fluently and have a child between the ages of 9 and 15 years old.
  • •Mothers must either have no history of psychopathology or have a history of depression during their child's lifetime.

Exclusion Criteria

  • •Eligible mothers cannot:
  • •currently be in treatment for drug or alcohol abuse
  • •have significant symptomatology related to psychopathology outside of depression
  • •have a medical history of neurological injury or impairment.
  • •Mothers who meet the requirements for inclusion in the control group must not have a history of any Axis I disorder.

Outcomes

Primary Outcomes

Onset of depression

Time Frame: 18 months

participants are interviewed in an 18-month follow-up session

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other

Study Sites (2)

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