Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
126 participants
INTERVENTIONAL
2023-11-21
2024-04-03
Brief Summary
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Method: The study will be completed in a randomized controlled manner with a total of 126 primiparous pregnant women, 63 in the experimental group and 63 in the control group. Pregnant women in the experimental group will focus on the Virgin Mary flower in the water-filled jar and imagine that their uterus and birth path are opening like the branches of the Virgin Mary flower that blooms as labor pains come. There will be no intervention in the control group other than routine midwifery care. Research data will be collected with the Pregnant Introduction and Birth Process Follow-up Form, Visual Analog Scale, and Visual Similarity Scale for Fatigue.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Maryam's Flower Group
Maryam's flower will place in a bowl of water and left in the room of the pregnant women who will at 1 cm cervical dilatation and in the first phase of the labor. It will explain to the pregnant women that the leaves of the plant would open up in the water, and they will ask to imagine that the birth canal would simultaneously open up. In effect, they will told to focus on the opening of these leaves during the course of the labor.. After birth, the flower used only as a focusing method will be removed from the water and its water will be poured.
Focusing on Maryam's Flower
Effect of Focusing on Maryam's Flower During the First Phase of the labor
control group
will provided with standard midwifery care.
No interventions assigned to this group
Interventions
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Focusing on Maryam's Flower
Effect of Focusing on Maryam's Flower During the First Phase of the labor
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* being in 37-42 weeks of pregnancy,
* being primiparous,
* having a single healthy fetus,
* cervical dilatation not more than 3 cm.the one which,
* in the first stage of labor,
* Does not have any complications preventing vaginal birth,
* volunteer women who do not have disabilities in communication and perception
Exclusion Criteria
* pregnant with assisted reproductive techniques,
* having a presentation anomaly,
* having a twin pregnancy,
* electing cesarean section,
* Women whose cervical dilatation exceeds 3 cm and who are not willing to participate in the study
18 Years
55 Years
FEMALE
Yes
Sponsors
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Ondokuz Mayıs University
OTHER
Responsible Party
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Sümeyye BAL
Ph.D.
Principal Investigators
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Sümeyye BAL
Role: STUDY_CHAIR
Ondokuz Mayıs University
Sümeyye BAL
Role: PRINCIPAL_INVESTIGATOR
Ondokuz Mayıs University
Locations
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Ondokuz Mayis University
Samsun, , Turkey (Türkiye)
Countries
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Other Identifiers
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2022/294
Identifier Type: -
Identifier Source: org_study_id
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