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Postpartum Depression clinical trials

View clinical trials related to Postpartum Depression.

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NCT ID: NCT00604604 Completed - Clinical trials for Postpartum Depression

Postpartum Depression Prevention Trial

Start date: August 2004
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the effect of peer (mother-to-mother) support on the prevention of postpartum depression among mothers identified as high-risk.

NCT ID: NCT00565032 Completed - Clinical trials for Postpartum Depression

Postpartum Thyroid Measures and Mood

Start date: January 2000
Phase: N/A
Study type: Observational

Women with abnormal serum thyroid antibody levels or abnormal TSH and/or T4 values are more likely than their normal counterparts to have higher scores on a common postpartum depression screening test.

NCT ID: NCT00560027 Completed - Clinical trials for Postpartum Depression

Case Management Study for Postpartum Depression and Intimate Partner Violence

Start date: July 2010
Phase: N/A
Study type: Interventional

The objective of the study was to assess the prevalence, timing, and co-occurrence of positive screens for maternal postpartum depression (PPD) and intimate partner violence (IPV) for women bringing their young infants for pediatric primary care and examine relationships between PPD, IPV and children's healthcare utilization from birth to 2 years.

NCT ID: NCT00384943 Completed - Clinical trials for Postpartum Depression

Study of Home-Based Exercise to Alleviate Postpartum Depression

Start date: November 2001
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of an aerobic home-based exercise program for the treatment of postpartum depression.

NCT ID: NCT00370903 Completed - Clinical trials for Postpartum Depression

Postpartum Depression and Cesarean Section

Start date: August 2006
Phase: N/A
Study type: Observational

The purpose of this retrospective study is to determine if there is an increase in postpartum depression (PPD) among women who undergo an emergency cesarean section as opposed to a planned cesarean section. We will analyze the hospital and clinic medical records of postpartum women who delivered by cesarean section (CS) at Tulsa Regional Medical Center between January 1, 2003, and June 1, 2005, and who obtained their postpartum care at the OSU Ob/Gyn Clinic in Tulsa, Oklahoma. We will record whether the cesarean was planned or emergent, and we will note the score they received on the Edinburgh Postnatal Depression Scale when they came to the clinic for their four-week postpartum visit. A score of 12 or lower on the EPDS will be considered "not depressed", and a score of 13 or higher will be considered "depressed." Numbers of depressed patients will be compared among the two types of cesarean sections and analyzed for statistical differences using the chi-squared method of analysis.

NCT ID: NCT00360204 Completed - Clinical trials for Postpartum Depression

Improving Health Outcomes for New Mothers and Babies

Start date: September 2006
Phase: Phase 3
Study type: Interventional

Because adherence to postnatal care guidelines across the United States (U.S.) is poor, newborns and mothers often are placed at undue risk for adverse medical and social outcomes. This study aims to evaluate an alternative model of care and improve healthcare delivery to and reduce health disparities for "well" newborns and mothers after hospital discharge by using single postnatal home nurse visits. The principal investigator has previously shown a reduction in poor outcomes for infants who receive a home visit after discharge when studied retrospectively. The proposed research will build on the previous study and prospectively evaluate the impact of a single home nursing visit on morbidities and health disparities for newborns and mothers in a randomized, controlled trial involving 1154 mother/infant breastfeeding dyads. Home visits should guarantee detailed assessment during an at-risk period of infancy and motherhood, where medical and social problems can be recognized, anticipated, and/or treated, and can bridge the gap between hospital care and primary care. The investigators' program, The Nurses for Infants Through Teaching and Assessment after the NurserY (NITTANY) Initiative, also will consider the cost-effectiveness of home visitation compared with guidelines-adherent outpatient clinic care.

NCT ID: NCT00298311 Completed - Clinical trials for Postpartum Depression

Effect of Home-Based Peer Support on Maternal-Infant Interaction and Postpartum Depression

Start date: November 2005
Phase: N/A
Study type: Interventional

The objective of this study is to examine the impact of a home-based peer support intervention for mothers affected by postpartum depression (PPD) and for their infants.

NCT ID: NCT00277108 Completed - Clinical trials for Postpartum Depression

Lexapro in the Treatment of Patients With Postpartum Depression

Start date: February 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if Escitalopram (Lexapro) is effective in the treatment of postpartum depression.