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Childbirth Problems clinical trials

View clinical trials related to Childbirth Problems.

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NCT ID: NCT06241443 Completed - Childbirth Problems Clinical Trials

Nursing Students & Positive Birth Perception & Simulation

Start date: September 20, 2022
Phase: N/A
Study type: Interventional

The study aimed to investigate the impact of simulation-based training on nursing students' perception of positive birth and natural birthing approaches.

NCT ID: NCT05711472 Completed - Labor Pain Clinical Trials

The Effect of Birth Ball Exercise on Labor Pain, Delivery Duration, Birth Comfort, and Birth Satisfaction

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

It has been reported that the birth ball has benefits such as decreasing the perception of labor pain, reducing the anxiety level, shortening the duration of the first stage of labor, increasing the satisfaction of birth, and facilitating the descent of the fetal head, but the literature is quite limited. So, this randomized controlled experimental study aimed to examine the effect of birth ball exercise on labor pain, delivery duration, birth comfort, and birth satisfaction.

NCT ID: NCT05529823 Completed - Parenting Clinical Trials

Showering During Labor

Start date: October 1, 2022
Phase: N/A
Study type: Interventional

The research covers the birth memory evaluation to determine the pregnancy process, the labor process and the changes in the perceived pain level during this process, the parenting behavior immediately after the birth and the process of the birth.

NCT ID: NCT04888013 Completed - Childbirth Problems Clinical Trials

Birth Environment and Childbirth-stress, Control & Outcome

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

This research improves the correlation between birth control and birth outcomes by understanding the childbirth environment and birth stress. A Quasi Experiment research . The sample size was calculated using a two-tailed test, the significance level α was 0.05, the power was 80%, three groups of repeated measurements were taken three times, the effect size (effect size) was set to medium.25, and the required number of samples was 108 people, resulting in a 20% wastage rate, a total of 129 people are needed, so each of the three groups is expected to accept 43 people.

NCT ID: NCT03687879 Completed - Pregnancy Related Clinical Trials

Women's Evaluation of the Childbirth Experience: From Pregnancy to Postpartum

EVA (ECE)
Start date: September 17, 2018
Phase:
Study type: Observational

Women report inappropriate health professional behaviour towards them during pregnancy or childbirth on social networks. However, to date, no data are available to estimate the number of women concerned. These data are necessary to characterize these behaviours to get out of this polemic and build a reflection on the improvement of the patient relationship and the emotional security of women.

NCT ID: NCT03461640 Completed - Labor Pain Clinical Trials

Community Based Doulas for Migrant Women in Labour and Birth in Sweden - a Randomised Controlled Trial

Start date: March 10, 2018
Phase: N/A
Study type: Interventional

One initiative to address communication problems between migrant women not fluent in Swedish and caregivers throughout childbirth is to provide language assistance, cultural interpretation and labour support to the woman through Community Based Doulas (CBDs). CBDs are bilingual women from migrant communities trained by midwives to provide cultural, language and labour support to migrant women throughout their labour and birth. The study will evaluate the effectiveness of community-based doula support for improving the intrapartum care experiences and postnatal wellbeing of Somali-, Tigrinya -, Arabic- and Russian-speaking migrant women giving birth in Stockholm, Sweden. The randomisation ratio will be 1:1; CBD support in addition to standard intrapartum care or standard intrapartum care. Women allocated to receive CBD support in addition to standard intrapartum care (intervention group), will be contacted by a Somali, Arabic-, Russian- or Tigrinya-speaking CBD as appropriate, and arrangements will be made for the doula and the women to meet twice prior to the birth to get to know each other and discuss the woman's wishes regarding support in labour and what the CBD can offer. Each woman will then contact her CBD when she goes into labour and the CBD will attend hospital with her and stay with her throughout labour and birth, in addition to any other support people she may have, such as her partner. Women allocated to the comparison arm of the trial will receive standard intrapartum care as provided at their chosen hospital of birth. The hypothesis is that women randomised to receive CBD support in labour will rate their care for labour and birth more highly and have better emotional wellbeing (lower mean scores on the Edinburgh Postnatal Depression Scale) two months after birth than women allocated to standard care.