Mothers With a History of Depression and Their 10-14 Year Old Daughters
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Purpose
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.
| Condition | Intervention |
|---|---|
|
Depression Depressive Disorder, Major |
Other: No intervention |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Prospective |
| Official Title: | The Neural Correlates of Mood and Cognitive Bias in a Population at Risk for Depression: Maternal Cognitive and Emotional Functioning |
- Onset of depression [ Time Frame: 18 months ] [ Designated as safety issue: No ]participants are interviewed in an 18-month follow-up session
Biospecimen Retention: Samples With DNA
All participants are asked to submit saliva samples during their second session using sterile salivette containers in order to assess cortisol levels. There is no risk involved in giving these samples.
| Enrollment: | 240 |
| Study Start Date: | February 2004 |
| Study Completion Date: | April 2011 |
| Primary Completion Date: | April 2011 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
children at risk for depression
children at familial risk for depression
|
Other: No intervention
there is no intervention for this study
|
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.
Eligibility| Ages Eligible for Study: | 9 Years to 15 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
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.
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.
Contacts and Locations| United States, California | |
| Stanford University Department of Psychology | |
| Stanford, California, United States, 94305 | |
| Stanford University School of Medicine | |
| Stanford, California, United States, 94305 | |
| Principal Investigator: | Ian H Gotlib, PhD | Stanford University Department of Psychology |
More Information
No publications provided
| Responsible Party: | Ian H. Gotlib, Principal Investigator, Stanford University School of Medicine |
| ClinicalTrials.gov Identifier: | NCT01129752 History of Changes |
| Other Study ID Numbers: | SU-03172010-5264, 13058 |
| Study First Received: | May 21, 2010 |
| Last Updated: | June 21, 2011 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Depression Depressive Disorder Depressive Disorder, Major |
Behavioral Symptoms Mood Disorders Mental Disorders |
ClinicalTrials.gov processed this record on June 18, 2013