Clinical Trials Logo

Postpartum Depression clinical trials

View clinical trials related to Postpartum Depression.

Filter by:
  • Not yet recruiting  
  • « Prev · Page 3

NCT ID: NCT05229913 Not yet recruiting - Clinical trials for Postpartum Depression

Effects of Esketamine on Postpartum Depression

EEPD
Start date: February 20, 2022
Phase: Phase 4
Study type: Interventional

Different concentrations of Esketamine were used after cesarean section. Through the evaluation of postoperative psychological status and analgesic effect, the optimal dosage of Esketamine to exert the effects of depression and analgesia was analyzed.

NCT ID: NCT05055674 Not yet recruiting - Clinical trials for Postpartum Depression

The Effects of Motherly on Postpartum Depression

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

Investigators will be test the efficacy of Motherly, a smartphone application (app) to treat depression in women with postpartum Depression. The Motherly app offers psychoeducation, mood and anxiety monitoring, several well-established psychological techniques (behavioral activation, cognitive restructuring, emotion regulation, stress management techniques, mindfulness and meditation, sleep hygiene), and helps mothers organize their medical appointments and keep track of their childrens' development. The efficacy of the Motherly app will be tested in a parallel two-arm randomized controlled trial. Participants will be randomly allocated to receive the Motherly app (intervention), or COMVC (active control), a smartphone app that delivers only psychoeducational content related to general mental health.

NCT ID: NCT04741971 Not yet recruiting - Quality of Life Clinical Trials

Whether Probiotics Use in Neonate and Infant Improve Their Mother's Life Quality

Start date: February 18, 2021
Phase: N/A
Study type: Interventional

Postpartum depression and poor quality of life during postpartum were an vital issue in recent years. Infant's health condition was thought to be a possible reasons related mother's postpartum quality of life, and functional gastrointestinal disorders such as infantile colic and regurgitation were common problem during infant period. Previous study revealed that probiotics may improve the infant's discomfort caused by functional gastrointestinal disorders. Thus, this study aimed to investigate whether probiotics use in neonate and infant improve their mother's life quality?

NCT ID: NCT04183946 Not yet recruiting - Clinical trials for Major Depressive Disorder

Willkommen Mutterglück: Online CBT for Pregnant and Postpartum Women With Depression and Anxiety

Start date: June 2020
Phase: N/A
Study type: Interventional

This intervention study aims to evaluate the effectivity of web-based cognitive therapy in reducing depression and anxiety in pregnant and postpartum women. Moreover, it aims to assess treatment feasibility and usability of the treatment in the same population. After an initial screening to determine the eligibility to participate, all participants fulfilling the inclusion criteria will receive their personal access login in order to start the intervention.

NCT ID: NCT02862444 Not yet recruiting - Clinical trials for Postpartum Depression

A Culturally Appropriate Intervention for Preventing and Reducing Postpartum Depression

Start date: August 2016
Phase: N/A
Study type: Observational

Postpartum depression (PPD) is a highly prevalent and serious mental health problem and is defined as the most recent episode of depression occurring between four weeks and twelve months after childbirth. PPD has negative effects, which are usually strongest during the first six months and may decrease the quality of mother-child interaction, adversely affecting the child's behavior and emotional and cognitive development, as well as the spouse marital relationship.PPD prevalence is estimated at 10 to 20%. A recent studies among Arab-Bedouin women, reported 31% - 43 of PPD. Aims: To develop and implement a culturally appropriate intervention program by using focus group (FGs) methodology Methods and Research program description: The study includes two phases. First, qualitative study will be conducted by using focus groups (FGs) method and based on the results of this phase we will develop a culturally based program. The second phase will include implementation and evaluation of the effectiveness of a culturally appropriate intervention.

NCT ID: NCT02191423 Not yet recruiting - Clinical trials for Postpartum Depression

Oxytocin and Dyadic Psychotherapy in the Treatment of Post Partum Depression

Start date: January 2015
Phase: N/A
Study type: Interventional

Rationale and Hypotheses of the Current Research: the investigators speculate that mothers suffering from PPD exhibit high levels of depression and low levels of OXT, hence experiencing the interaction with their child as less rewarding, which in turn promote further depressive symptoms and interfere with child development. While dyadic psychotherapy has been studied in this context, it is unknown which depressed women will respond to this type of therapy, and whether such a response is mediated by the pro-bonding effect of oxytocin. The aim of this study is three-fold: 1. To study the effect of the administration of a single dose (24IU) of oxytocin on cerebral circuit processing and connectivity of empathy and attachment. 2. To examine whether the clinical response of mothers suffering from postpartum depression to short term dyadic psychotherapy (based on improved mother-child interactions) can be predicted by a unique brain response pattern to oxytocin. 3. To assess the relationship between levels of oxytocin in mother and baby and the effectiveness of psychological dyadic treatment on mothers suffering from postpartum depression.

NCT ID: NCT01658098 Not yet recruiting - Clinical trials for Postpartum Depression

Prevalence of Postpartum Depression in Hospital Jose E. Gonzalez

Start date: September 2012
Phase: N/A
Study type: Observational

This research will use the Edinburgh Scale Of Post partum depression to evaluate patients during their 4th to 6th after delivery, and the investigators will compare the results with those found in other countries with population with similar characteristics as ours

NCT ID: NCT01423331 Not yet recruiting - Clinical trials for Postpartum Depression

An Evaluation and Factor Analysis for Maternal Mental Health

Start date: August 2011
Phase: N/A
Study type: Observational

An Evaluation and Factor Analysis for Maternal Mental Health - The Analytic Study of the Shin Kong Wu Ho-Su Memorial Hospital - Objectives: 1. To construct a screening tool for domestic maternal mental health 2. To expect to find the screening timing for early assessment or intervention of domestic maternal mental health status. 3. To explore the impact of domestic maternal mental health factors.