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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01129752
Other study ID # SU-03172010-5264
Secondary ID 13058
Status Completed
Phase N/A
First received May 21, 2010
Last updated June 21, 2011
Start date February 2004
Est. completion date April 2011

Study information

Verified date June 2011
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 240
Est. completion date April 2011
Est. primary completion date April 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 9 Years to 15 Years
Eligibility 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.

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Intervention

Other:
No intervention
there is no intervention for this study

Locations

Country Name City State
United States Stanford University Department of Psychology Stanford California
United States Stanford University School of Medicine Stanford California

Sponsors (2)

Lead Sponsor Collaborator
Stanford University National Institute of Mental Health (NIMH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Onset of depression participants are interviewed in an 18-month follow-up session 18 months No
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