Mindfulness Breath Awareness Meditation & Preeclampsia

Status Recruiting

Clinical Trial Summary

The effect of mindfulness breath awareness meditation on health profile, vital signs, and fetal heart rate in pregnant women with preeclampsia

Clinical Trial Description

The aim of this study is to determine the effect of mindfulness breath awareness meditation (MBAM) on health profile, vital signs, and fetal heart rate in pregnant women with preeclampsia. Sample size: - There will be two groups in the study. - Experiment group is breath awareness meditation group. - The sample size of the study is 66 women. - The sample size will be divided into two and 33 women will be randomly assigned to each group. Application time: - The application will be started after the pregnant women diagnosed with pre-eclampsia is admitted to the Perinatology service. - It will be applied total nine times in once every eight hours during the 72 hours that the pregnant women diagnosed with 20 minutes. - Only mindfulness breath awareness meditation (MBAM) will not be applied to the control group. Care and follow-up will be performed in parallel with the individuals in the experimental group. Data Collection Tools: - Descriptive Information Form - Nottingham Health Profile Scale Measurement time: - Pregnant women will fill in the Introductory Information Form before the first application. - Each session of mindfulness breath awareness meditation practice will 20 minutes. - Pregnant women will fill the Nottingham Health Profile Scale before the first application. It will then be refilled at the same time every 24 hours for 72 hours. The Nottingham Health Profile will be completed a total of four times. - Vital signs (systolic and diastolic blood pressure, body temperature, pulse, respiration, oxygen saturation) will be measured immediately before the first application. They will then be refilled at the same time every 24 hours for 72 hours. Vital signs will be completed a total of four times. - Fetal heart rate and fetal movement count will be measured immediately before the first application. They will then be refilled at the same time every 24 hours for 72 hours. Fetal heart rate and fetal movement count will be assessed by Non-stress Testing (NST). The pregnant woman will undergo NST for 20 minutes. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06065709
Study type	Interventional
Source	University of Gaziantep
Contact
Status	Recruiting
Phase	N/A
Start date	October 1, 2023
Completion date	April 1, 2024

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See also
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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Mindfulness Breath Awareness Meditation and Preeclampsia

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms