Post-partum Depression Clinical Trial
Official title:
Mobile Application in the Management of Mild to Moderate Postpartum Depression (PPD)
Primary Objective: Evaluate the user experience with the Stella (TM) app for the management of Postpartum Depression in an observed population for 8 calendar weeks.
Women between 18 and 50 years of age who have had a live birth within 4 months prior to study start date and have a diagnosis of mild to moderate PPD. A total of 65 women residing in the state of New York, New Jersey and Connecticut will be recruited to participate in the study. Patient reported outcomes of mild to moderate depression (using EPDS) will be verified by a behavioral health therapist using the Hamilton Depression Rating Scale (HAM-D). ;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT01178008 -
Pilot Study on the Use of Acupuncture for Postpartum Depression
|
N/A | |
| Active, not recruiting |
NCT03416010 -
Healthy Lifestyle Intervention for High-Risk Minority Pregnant Women
|
N/A | |
| Withdrawn |
NCT02738021 -
Managing PPD at Gouverneur
|
N/A | |
| Recruiting |
NCT06208852 -
Virtual Patient Navigation During a Pandemic
|
N/A | |
| Withdrawn |
NCT02741206 -
Preventing Postpartum Depression in Prenatal Care
|
N/A | |
| Completed |
NCT00373750 -
Cradling Our Future Through Family Strengthening Study
|
N/A | |
| Recruiting |
NCT05518162 -
Treatment of Post-partum Depression Using an Behavioral Intervention Called ROSE (Reach Out, Stay Strong, Essentials for Mothers of Newborns) Delivered Using an Electronic App
|
N/A | |
| Not yet recruiting |
NCT06131255 -
DRACULA1 Partum Depression: an Integrated Molecular-pharmaco-imaging Study")
|
||
| Not yet recruiting |
NCT06285916 -
A Study to Assess the Efficacy, Safety, and Tolerability of Oral NORA520 in Adults With Severe Postpartum Depression
|
Phase 2 | |
| Completed |
NCT01407783 -
Systems of Care for New Moms: Integrating Depression Treatment
|
N/A |