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Depression, Postpartum clinical trials

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NCT ID: NCT05399784 Completed - Breastfeeding Clinical Trials

Postpartum Visit Timing and the Effect on Visit Attendance

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

The objective of this study is to assess if the addition of an early postpartum visit improves attendance at postpartum visits. We seek to evaluate if an additional early postpartum visit improves patient education, satisfaction, or trust in the clinicians during the postpartum period; all of which may ultimately facilitate improved outcomes. Additionally, we seek to explore patient preferences for postpartum care delivery.

NCT ID: NCT05382884 Completed - Clinical trials for Postpartum Depression

The SUPPORT Study: Effectiveness and Usability of a Web-Enabled Resource for Postpartum Mental Health

SUPPORT
Start date: April 20, 2022
Phase: Phase 2
Study type: Interventional

The SUPPORT Study aims to evaluate the effectiveness and usability of postpartumcare.ca, a web-enabled resource for postpartum depression (PPD) and postpartum anxiety (PPA), created based on the input of birthing parents in British Columbia (BC) affected by these disorders.

NCT ID: NCT05362305 Recruiting - Clinical trials for Postpartum Depression

Essential Coaching for Every Mother in Tanzania

ECEMTZ
Start date: June 13, 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate a text message intervention called Essential Coaching for Every Mother in Tanzania to improve mothers' access to essential newborn care information during the immediate six-week postnatal period.

NCT ID: NCT05356026 Completed - Clinical trials for Postpartum Depression

Online Postpartum Follow-up on Depression and Postpartum Adaptation

Start date: March 10, 2021
Phase: N/A
Study type: Interventional

Objective: To determine the effect of online postpartum follow-up on depression and postpartum adaptation. Design: A parallel-randomized-controlled study Setting: During 2021 in Turkey Participants: 52 women in the postpartum period Measurements: Data were collected through the Personal Information Form, the Follow-up Form, the Edinburgh Postpartum Depression Scale (EPDS), and the Postpartum Self-Assessment Scale (PSAS). The women in the experimental group were administered three follow-ups (education/consultancy) in line with the timing and content in the T.R. Ministry of Health Postpartum Care Management Guide (2014). The follow-ups were performed using the Zoom® program, which enabled video talk. The women in the control group received the routine follow-up and care provided by the hospital.

NCT ID: NCT05353491 Active, not recruiting - Clinical trials for Depression, Postpartum

Thinking Healthy Program-Technology Assisted (THP-TA)

THP-TA
Start date: June 13, 2022
Phase: N/A
Study type: Interventional

Background The Thinking Healthy Program (THP) is an evidence based task-shifted low intensity psychosocial intervention, recommended by the World Health Organization for the treatment of perinatal depression. The investigators developed a technology-assisted version of Thinking Healthy Program (THP-TA) which allows peers to deliver the THP, while ensuring minimal resources for training of delivery agents and ensuring adequate fidelity. Method This is a non-inferiority, pragmatic cluster randomized controlled trial designed to test the primary hypothesis that technology assisted delivery of THP is not worse than THP intervention delivered by community health workers, in increasing perinatal depression remission rates at 3 months postnatal. In addition, this study will also test the effectiveness of the THP-TA in improving recovery from perinatal depression at 6 months postpartum, quality of life and social support. This study also aims to evaluate the cost-effectiveness of the THP-TA.

NCT ID: NCT05322161 Completed - Depression Clinical Trials

Yoga in the NICU for Parents Study

YiN
Start date: September 29, 2021
Phase: N/A
Study type: Interventional

The purpose of this proposal is to test the efficacy of yoga as a mind and body intervention to decrease stress, anxiety, and depression in parents of critically ill neonates hospitalized in the Seattle Children's and University of Washington neonatal intensive care units (NICUs).

NCT ID: NCT05314361 Completed - Clinical trials for Postpartum Depression

Public Health Nurse-Delivered 1-Day CBT Workshops Pilot

Start date: March 18, 2022
Phase: N/A
Study type: Interventional

Public Health Nurses received training to deliver a day-long Cognitive Behavioural Therapy-based workshop for treating postpartum depression. Participants in the study are randomly assigned to the treatment group (1-day CBT workshop) or control group (usual postnatal care). Data will be collected from all participants at baseline, 3 and 6 months. The study will aim to assess the feasibility of our methods and estimate the treatment effect of the primary outcome in preparation for a larger RCT. Objectives include: - Recruit and randomize 96 participants within 5 months - Questionnaire completion - 75% of participants complete all three questionnaires and structured interviews - Retention - 75% of participants remain in study until completion - 75% of participants in treatment group complete the intervention - Estimate treatment effect and variance

NCT ID: NCT05299398 Not yet recruiting - Clinical trials for Postpartum Depression

Prevention of Postpartum Depression: A Pilot Placebo-controlled Trial of Trazodone

Start date: September 1, 2022
Phase: Phase 1
Study type: Interventional

Postpartum depression is a serious illness that affects approximately 17% of women who have recently given birth. Untreated depression appears to have negative effects for both the mother and her baby. Postpartum depression is quite common among women with a history of depression. Sleeplessness is a common concern during pregnancy and after delivery, and it can also trigger depression in women with a history of depression. Antidepressants are the most commonly recommended drugs for prevention of postpartum depression; however, there is limited research to understand the effectiveness of the medications in preventing postpartum depression. Trazodone is a weak antidepressant, but it is commonly prescribed for sleeplessness due to physical or psychiatric disorders. We are planning a study to find out whether trazodone in a low dose is more effective than a sugar pill in preventing postpartum depression among women with histories of depression. We expect the results of our study will make it easier for healthcare providers to select the right medication for women who are at risk of developing depression after delivery and thus improve the mental health of mothers and well-being of their babies.

NCT ID: NCT05295069 Completed - Clinical trials for Sleep Quality, Depression, Postnatal Care, Single-Blind Method, Fatigue, Social Support

Can Postpartum Depression Be Prevented With Care

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

This study was designed to eliminate postpartum insomnia and fatigue and reduce the risk of postpartum depression through the maintenance of structural, personal, and social integrity with holistic care under the guidance of Levine's conservation model for primiparous puerperal women who experience fatigue and are at risk of developing depression. : A single-blind pretest-posttest randomized controlled study. Women were called to the hospital on the 7th postpartum day and randomly assigned by a computer program to either the intervention group (n=56) or the control group (n=56). Participants did not know which group they were in.

NCT ID: NCT05285215 Recruiting - Clinical trials for Depression, Postpartum

Integrated Psychological Program for Management of Postnatal Depression and Persistent Postpartum Pain After Childbirth

CODEPAD-II
Start date: April 18, 2022
Phase: N/A
Study type: Interventional

The integrated psychological program (IPP) is based on evidence from the local population showing that the interventional components (mindfulness training, music listening, video counselling) are amenable to implementation in the outpatient care setting. Incorporating innovative digital mobile and electronic applications in the care of an increasingly technology-savvy population will be strategic. The proposal will transform the healthcare model for treating postnatal depression (PND) and persistent postpartum pain (PPP).