Status:
COMPLETED
T- BOOM Teens--Building Options and Opportunities for Moms
Lead Sponsor:
University of Pittsburgh
Conditions:
Postpartum Major Depression
Eligibility:
FEMALE
10-17 years
Phase:
NA
Brief Summary
Postpartum depression (PPD) is depression that occurs shortly after the mother delivers her baby. Mothers with postpartum depression may feel sad mood, low motivation or stress; some may have problems...
Detailed Description
Depression during the perinatal period is a major public health concern. Postpartum depression (PPD) causes personal and family suffering at a time when adaptation to parenthood is critical. Successfu...
Eligibility Criteria
Inclusion
- Adolescent mothers age \< 17 years 364 days at birth of index infant
- Live born infants
- Parents/guardian of the young mother must be available and competent to provide consent to the enrollment of the young mother
- The young mother may provide assent for her own enrollment.
- Ethical need for awareness of the possible risks, benefits and alternatives to enrollment in this study.
- Mothers with an EPDS\>/=10 or CES-D\>/=16 (suggest increased risk for major depression)
- Mothers with major depressive disorder (MDD) regardless of their EPDS or CES-D scores. These are patients with high risk for severe recurrence of depressive symptoms in the postpartum. We will assess their outcomes in this study.
- Adolescent mothers with an EPDS\<10 OR CES-D\<16 (screen negative) without MDD will be interviewed by phone with the KIDDIE-SADS mood screen to screen for all categories of major diagnoses AND the Mood Disorders Module
Exclusion
- No access to a telephone Screening and depression care management are accomplished by phone; mothers with no phone are referred to Magee social work for other services
- NON-English-speaking Measures are in English
- The multiple questionnaires and measures are in English
Key Trial Info
Start Date :
April 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2010
Estimated Enrollment :
23 Patients enrolled
Trial Details
Trial ID
NCT00745537
Start Date
April 1 2008
End Date
December 1 2010
Last Update
May 28 2015
Active Locations (1)
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1
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania, United States, 15213