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Postpartum Depression clinical trials

View clinical trials related to Postpartum Depression.

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NCT ID: NCT00804739 Completed - Clinical trials for Postpartum Depression

Perinatal Depression Treatment in a Pediatric Setting- Pilot Phase

MITT
Start date: January 2009
Phase: N/A
Study type: Interventional

The purpose of this project is to test whether a new model of collaborative care depression treatment adapted to the needs and preferences of low-income, urban mothers with perinatal depression and to a pediatric clinic setting increases engagement in and adherence to perinatal depression treatment.

NCT ID: NCT00795652 Completed - Clinical trials for Postpartum Depression

Mom: Managing Our Mood, Part of The Family Help Program

MOM
Start date: May 2006
Phase: Phase 2
Study type: Interventional

The purpose of the MOM: Managing Our Mood Program (part of Family Help) is to evaluate the effectiveness of the Family Help distance intervention compared to usual or standard care typically provided to women with mild to moderate postpartum depression symptomology. This is a single-center trial based at the IWK Health Center. The primary outcome is change in postpartum depression diagnosis.

NCT ID: NCT00782912 Completed - Clinical trials for Postpartum Depression

Postpartum Anemia and Postpartum Depression

PPADS
Start date: November 2008
Phase:
Study type: Observational

Postpartum anemia (PPA) and Postpartum depression (PPD) are common afflictions affecting women after childbirth. Both disorders have a significant impact on women's health and functional status. Despite common symptoms and characteristics, a link between these entities has not been adequately studied. The objective of this study is to determine whether postpartum anemia is an independent risk factor for the development of postpartum depression. This prospective cohort study will include all women delivered by elective term cesarean delivery. Hemoglobin and iron levels will be measured, standardized questionnaires for assessment of PPD, functional status and lactation will be administered before discharge and at 3 & 6 weeks post partum. Hemoglobin levels at each time point will be analyzed for correlation with depressive symptoms, functional status and lactation success.

NCT ID: NCT00744328 Terminated - Clinical trials for Postpartum Depression

Postpartum Depression: Transdermal Estradiol Versus Sertraline

E2SERT
Start date: August 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether estrogen patches are effective for the treatment of postpartum major depression, as compared to sertraline (Zoloft) and placebo.

NCT ID: NCT00617045 Withdrawn - Clinical trials for Major Depressive Disorder

Duloxetine for the Treatment of Postpartum Depression

DuloxPPD
Start date: July 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether the antidepressant, duloxetine, is equally effective as a treatment for subjects who have a Postpartum Onset Depression compared to subjects who have an onset of Major Depressive Disorder prior to delivery. The hypothesis is that duloxetine will be as effective in subjects with Postpartum Major Depressive Disorder as in subjects with a Major Depressive Disorder.

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: NCT00548743 Unknown status - Clinical trials for Postpartum Depression

Translating Research Into Practice for Postpartum Depression

TRIPPD
Start date: September 2005
Phase: N/A
Study type: Interventional

This is a study to assess the impact of introducing screening and planned follow up for postpartum depression. All women ages 18 to 45 who speak English or Spanish who come to the enrolled community family medicine offices will either be given usual care or screened using the Edinburgh Postnatal Depression Screening tool. If the EDPS score is high the women will be given the PHQ-9 to more clearly identify the specific likelihood of being depressed. Women who are determined to be depressed will be treated with medication or counseling based on the preference of the women and their physicians. Women will be followed through nurse initiated phone calls and visits to the physicians office. Outcomes include the level of depression symptoms, measure of comfort with parenting, and satisfaction with partner relationships comparing baseline levels with those at 6 and 12 months from the usual care and intervention sites. These data will be collected by questionnaire. In addition, with the women's permission, medical records will be reviewed.

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.