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First Birth clinical trials

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NCT ID: NCT06199245 Recruiting - Breastfeeding Clinical Trials

The Effect of Emotional Freedom Technique on Breastfeeding Success and Self-Efficacy

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

This study was planned to determine the effect of emotional freedom technique (EFT) on breastfeeding success and self-efficacy in primiparous women in the early postpartum period who had a cesarean delivery.

NCT ID: NCT06164613 Recruiting - Clinical trials for Labor Onset and Length Abnormalities

Use of Cinnamomum Verum for Induction of Labor. Double Blind Randomized Clinical Trial

CINNALAB
Start date: December 4, 2023
Phase: Phase 2
Study type: Interventional

The purpose of the research protocol is to evaluate the effectiveness of Cinnamomum verum extract for the initiation of labor. Cinnamaldehyde ((E)-3-Phenylprop-2-enal) is an α, β unsaturated aromatic aldehyde, derived from cinnamon (Cinnamomum Verum oil) used as a flavoring; It is a clear yellowish liquid substance, with a strong odor and flavor. It is the main component of cinnamon (63%), giving it its physicochemical properties. Cinnamon has been an element of empirical use for the beginning of labor, however, its effectiveness has not been demonstrated. Cinnamon has been reported for its ethnopharmacological properties in pregnancy, being used to facilitate childbirth, as a lactagogue and for postpartum recovery. In Honduras, its use has been reported to relieve nausea and vomiting during pregnancy, to reduce abdominal pain. , reduction of lower limb edema, to relieve anxiety during labor, as well as a lactagogue without convergent opinions.

NCT ID: NCT05948150 Completed - Clinical trials for Cesarean Section; Dehiscence

The Effect of Breastfeeding Pillow on Breastfeeding Self-Efficacy and Postpartum Comfort in Women Who Had Cesarean

Start date: November 29, 2022
Phase: N/A
Study type: Interventional

The research is a randomised controlled experimental study. It was conducted to examine the effect of breastfeeding pillow on breastfeeding self-efficacy and postnatal comfort in primiparous puerperas who gave birth by caesarean section. The answers to the questions "Is the breastfeeding pillow effective on breastfeeding self-efficacy in primiparous puerperium giving birth by caesarean section?" and "Is the breastfeeding pillow effective on comfort during breastfeeding in primiparous puerperium giving birth by caesarean section?" are investigated. The puerperas in the experimental group were allowed to use a breastfeeding pillow during breastfeeding and evaluated at 24th and 48th hours. Puerperas in the control group continued routine breastfeeding and did not use a breastfeeding pillow. They were evaluated at 24th and 48th hours.

NCT ID: NCT05533021 Completed - Cesarean Section Clinical Trials

Meleis's Transition Theory on Postpartum Difficulties and Quality of Life in Primipara Mothers

Start date: July 15, 2020
Phase: N/A
Study type: Interventional

The randomized controlled experimental study sought to determine the impact of the training structured according to Meleis's Transition Theory on postpartum difficulties and quality of life in primipara mothers.

NCT ID: NCT04591730 Terminated - Fathers Clinical Trials

First-time Fathers' Experiences of Childbirth in Lorraine

PRIMIPERE
Start date: October 12, 2020
Phase:
Study type: Observational

The primary aim of this study is to evaluate first time father's experience during childbirth in three different maternity hospitals in Lorraine. Secondary aims of this study is to identify domains that need improvement in order to enhance fathers's experience during childbirth.

NCT ID: NCT03594526 Completed - Mothers Clinical Trials

Efficacy of a Nursing Intervention in First-time Mothers

Start date: November 2, 2018
Phase: N/A
Study type: Interventional

Experimental study will determine the efficacy of nursing intervention named Maternal support to become first-time mothers based on the theory of Ramona Mercer. Sequential explanatory design will be used. It is a mixed design with approach quantitative and qualitative in order to obtain a better approach of the phenomen. The approach quantitative will be randomized controlled clinical trial. The qualitative analysis of the content will be done according to Bardin.