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Pregnancy, High Risk clinical trials

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NCT ID: NCT05946252 Completed - Clinical trials for Pregnancy, High Risk

Motor Imagery in High-Risk Pregnants

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

The aim of this study is to determine the acute effects of motor imagery exercises on fetal heart rate, uterine contractions, maternal heart rate, blood pressure, oxygen saturation and well-being in high-risk pregnant women.

NCT ID: NCT05653362 Completed - Clinical trials for Pregnancy, High Risk

Coconut Oil vs. Commercial Ultrasound Gel In Obstetric Ultrasounds

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

The goal of this randomized controlled trial is to compare the use of coconut oil with commercial ultrasound gel for obstetrical ultrasounds. The main questions it aims to answer are: 1. To evaluate the quality of ultrasound images obtained using coconut oil compared with commercial ultrasound gel. 2. To access patient acceptability of coconut oil as compared to commercial ultrasound gel. Participants will: 1. Allow a total of 6 study images to be obtained; 3 using coconut oil and 3 with commercial ultrasound gel. 2. Fill out a 10-question, 5-point Likert scale survey following their ultrasound with both coupling mediums to compare acceptability.

NCT ID: NCT05573009 Completed - Clinical trials for Depression, Postpartum

The Effect of Stress Reduction Program on Pregnancy Process and Mental Health in High Risk Pregnant Women

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

Introduction Pregnancy and giving birth to an infant is a physiological process as well as it is also a transition of life, and a stressful period of time with a significance in the life of woman. This period is evaluated as a developmental crisis for the woman, and for her family. High-risk pregnant women are at the forefront of the individuals who need to be supported the most during the transition to motherhood.The presence of a physiological, emotional and psychosocial condition that endanger the health and life of the pregnant and/or fetus and increases the risk of illness and death is defined as "high-risk pregnancy". Exposure to obstetric complications is known to be associated with the later development of psychiatric disorders. In the literature review, it is seen that there are few studies in which CBT and mindfulness-based interventions are applied to reduce stress, anxiety and depression in risky or risk-free pregnant women. However, no CBT-based stress reduction program applied to high-risk pregnant women has been found in our country. A stress reduction program based on cognitive behavioral interventions during the transition to motherhood can contribute to the protection of maternal mental health and psychological well-being in pregnant women, and may help for healthy pregnancy and birth outcomes. Research Aim This study was planned to examine the effect of cognitive behavioral approach-based stress reduction program on pregnancy process and maternal mental health to be applied to high-risk pregnant women. Research Type The study was planned as an experimental study with a randomized control group including pre-test, post-test and follow-up measurements to examine the effect of "stress reduction program based on cognitive behavioral approach" on the maternal mental health, pregnancy, and childbirth process of the high risk pregnant women.

NCT ID: NCT05317065 Completed - Stress Clinical Trials

The Effect of Mindfulness-Based Stress Reduction Program (MBSR) in Risky Pregnants

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

Risky pregnant women need various physical and mental health needs, they need to be informed and supported by health personnel. Mindfulness is a non-judgmental and accepting focus of one's attention on what is happening right now. A total of 100 pregnant women (50 experimental, 50 control) are planned to be included in the study. Data will be collected with "Descriptive Information Form", "Prenatal Distress Scale (PBL)-Revised Version", "Pregnancy-Related Anxiety Scale-Revision 2" and "Prenatal Attachment Inventory". In the study, a stress reduction program (MBSR) based on mindfulness will be applied by the researcher to the pregnant women in the experimental group.

NCT ID: NCT05316415 Completed - Sleep Quality Clinical Trials

The Effects of Music on the Anxiety and Sleep Quality of Pregnant Women on Bed Rest for a High-risk Pregnancy

Start date: September 15, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to identify the effects of music on the anxiety and sleep quality of women with high-risk pregnancy having bed rest in the hospital in Turkey. This randomized-controlled study involved 80 control and 80 experimental group with a high-risk pregnant woman .

NCT ID: NCT04874285 Completed - Clinical trials for Pregnancy, High Risk

Use of Dietary Supplements in Patients at Risk of Abortion Treated With Progesterone.

Start date: May 3, 2021
Phase: N/A
Study type: Interventional

The trial aims to investigate the effect of supplementation with hyaluronic acid, alpha-lipoic acid, magnesium, vitamin D and vitamin B6 in progesterone-treated pregnant women with risk factors for abortion.

NCT ID: NCT04783480 Completed - Clinical trials for Pregnancy, High Risk

Can Birthly, an Online Childbirth Education Platform, Reduce Pregnancy-related Anxiety Compared to Usual Care

Birthly
Start date: April 12, 2021
Phase: N/A
Study type: Interventional

A pilot randomized, controlled trial comparing Birthly, (an online platform for live group prenatal classes taught by childbirth educators, nurses, and lactation consultants) plus standard prenatal care versus standard prenatal care alone among women with high risk pregnancies.

NCT ID: NCT04687436 Completed - Cervical Ripening Clinical Trials

Foley Catheter Versus Double-balloon Catheter for Cervical Ripening

Start date: July 1, 2020
Phase:
Study type: Observational

The objective of this study is to compare pregnancy results which were used foley catheter or double-balloon catheter for cervical ripening among high-risk pregnant women.

NCT ID: NCT04599075 Completed - Type 1 Diabetes Clinical Trials

Intravenous Insulin vs Subcutaneous Insulin Infusion in Intrapartum Management of Type 1 Diabetes Mellitus

Start date: March 15, 2021
Phase: Phase 4
Study type: Interventional

The purpose of this study is to perform a randomized trial to investigate if intrapartum insulin delivery mechanisms reduces adverse outcomes associated with type 1 diabetes in pregnancy. The investigators aim to compare subcutaneous insulin pump versus intravenous insulin infusion with regard to the primary outcome of neonatal blood sugar.

NCT ID: NCT04571190 Completed - Clinical trials for Pregnancy, High Risk

An Adapted Mindfulness-based Stress Reduction Program for Psycho-socially Vulnerable Pregnant Women.

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

This protocol is for a feasibility study of an adapted mindfulness-based stress reduction (MBSR) program for high-risk pregnant women. The aim is to address the need for more evidence-based options for mental healthcare in pregnancy. MBSR has good evidence in reducing stress, anxiety and depression in both clinical and non-clinical populations, but has not yet been adapted for high-risk pregnancies. The purpose is to evaluate the feasibility, acceptability and potential intervention effects of an adapted MBSR program compared to usual care to inform a randomized controlled trial.