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Depression, Postpartum clinical trials

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NCT ID: NCT05206552 Recruiting - Clinical trials for Maternal Care Patterns

The Correlation Between Maternal Infant Bonding, Pain and Postpartum Depression

Start date: January 25, 2022
Phase:
Study type: Observational

The delivery process can be associated with significant maternal pain. which has many long and short term affects. The aim of our study is to assess whether pain during and after childbirth negatively impacts a mother's attachment to her baby (maternal bonding) and the increases the incidence of postpartum depression.

NCT ID: NCT05137925 Recruiting - Pregnancy Related Clinical Trials

Mindful Moms: Mechanisms of Mindfulness-based Cognitive Therapy During Pregnancy and Postpartum

Start date: September 1, 2023
Phase: N/A
Study type: Interventional

The proposed study seeks to elucidate the mechanisms underlying Mindfulness-Based Cognitive Therapy in pregnancy to improve understanding of how and why this treatment modality enhances well-being, which can then be leveraged to optimize treatment for psychological distress emerging during this vulnerable period.

NCT ID: NCT05097586 Recruiting - Pregnancy Clinical Trials

RCT of At-Home tDCS for Depression in Pregnancy

Start date: November 8, 2021
Phase: N/A
Study type: Interventional

This is a randomized, sham-controlled trial to determine whether treatment with transcranial direct current stimulation (tDCS) is superior to a sham condition at reducing the symptoms of depression in pregnant people with moderate to severe depression. The study aims to enrol 156 participants across all sites. Data collection occurs at baseline, immediately after treatment, every 4 weeks during pregnancy and 4-, 12-, 26- and 52-weeks postpartum

NCT ID: NCT05077644 Recruiting - Clinical trials for Post-partum Depression

Mobile Application in the Management of Mild to Moderate Postpartum Depression (PPD)

Start date: October 1, 2021
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT05050266 Recruiting - Obesity Clinical Trials

Enhancing Mental and Physical Health of Women Veterans

EMPOWER
Start date: October 21, 2021
Phase: N/A
Study type: Interventional

Women Veterans are the fastest growing segment of VA users. This dramatic growth has created challenges for VA to ensure that appropriate services are available to meet women Veterans' needs, and that they will want and be able to use those services. The EMPOWER QUERI 2.0 Program is a cluster randomized type 3 hybrid implementation-effectiveness trial testing two strategies designed to support implementation and sustainment of evidence-based practices for women Veterans in up to 20 VA facilities from 4 regions.

NCT ID: NCT05038085 Recruiting - Clinical trials for Postpartum Depression

Postpartum Depression and Maternal Attachment

Start date: October 25, 2021
Phase: N/A
Study type: Interventional

In terms of postpartum care and depression, follow-up and controls should be continued online in order not to interrupt the follow-up and treatment of women. In this context, in order to prevent the development of postpartum depression and to increase maternal attachment, it is planned to deliver the progressive muscle relaxation exercise and individual health education program that we planned in our study through online applications. This study will be conducted to evaluate the effect of online health education and progressive muscle relaxation exercise program on postpartum depression and maternal attachment.The study was planned as a parallel randomized controlled experimental study conducted in a Family Health Center in Ankara, with a single-center, stratified block randomization (parity: primiparous, multiparous; EPDS score: 0-9, 10-30).The number of pregnant women to be included in the study was calculated as 56.Personal Information Form, Prenatal Attachment Scale, Edinburgh Postpartum Depression Scale and Postpartum Attachment Scale will be used to collect data.

NCT ID: NCT04998721 Recruiting - Anxiety Clinical Trials

A Dyadic Approach to Perinatal Depression in Primary Care: Maternal Infant and Dyadic Care

MInD
Start date: November 1, 2022
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the effectiveness of a parenting intervention+usual care compared to usual care on postpartum depression and other mental health and parenting outcomes, as well as the feasibility and acceptability of the parenting intervention.

NCT ID: NCT04964206 Recruiting - Labor Pain Clinical Trials

Neuraxial Labor Analgesia and Offspring Neurodevelopment

Start date: October 14, 2022
Phase:
Study type: Observational [Patient Registry]

How perinatal factors affect the long-term development of children has always been an issue of much concern. This study is designed to explore the potential impact of maternal neuraxial labor analgesia exposure on offspring neurodevelopment.

NCT ID: NCT04950868 Recruiting - Clinical trials for Postpartum Depression

The Safety, Tolerability, and Effectiveness of Quetiapine in Postpartum Depression

Start date: March 18, 2022
Phase: Phase 1
Study type: Interventional

Postpartum depression is a serious disorder that affects approximately 14% of women who have recently given birth. Postpartum depression is either an episode of major depressive disorder (only low periods) or bipolar disorder (periods of lows and highs). Untreated postpartum depression can negatively affect the mother, the infant and the family. Antidepressants are the most used treatments; however, for many women these drugs are not useful, resulting in a pressing need for effective treatments for postpartum depression. Lack of sleep is common after delivery and can trigger depression in some women. Quetiapine, a drug used for bipolar disorder, major depressive disorder and occasionally sleeplessness has not been well studied in postpartum depression. This study aims to find out how mothers tolerate the drug and whether it is effective for postpartum depression. Results of this study may help investigators carry out a larger study comparing quetiapine and placebo (a sugar pill) in postpartum depression.

NCT ID: NCT04860661 Recruiting - Clinical trials for Postpartum Depression

Esketamine on Postpartum Depression in Cesarean Section Women

EKET
Start date: May 1, 2021
Phase: N/A
Study type: Interventional

This study was to explore the preventive effect of esketamine on postpartum depression in cesarean section, and to evaluate the safety of the drug