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Focusing on the Maryam's Flower During the Birth

The Effect of Focusing on the Maryam's Flower During the Birth Process on Labor Pain, Labor Duration and Perceived Fatigue in Birth

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06128759
Enrollment
126
Registered
2023-11-13
Start date
2023-11-21
Completion date
2024-04-03
Last updated
2024-10-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Labor Pain

Brief summary

To determine the Effect of Focusing on the Virgin Mary Flower during the Birth Process on Labor Pain, Labor Duration and Perceived Fatigue in Birth. 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.

Detailed description

Design and Settings: This randomized controlled experimental study will conducted in the delivery room of the, Turkey between the dates of November 2023 and April 2024

Interventions

OTHERFocusing on Maryam's Flower

Effect of Focusing on Maryam's Flower During the First Phase of the labor

Sponsors

Ondokuz Mayıs University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Being 18 years or older, * 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

* maternal and fetal complications * 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

Design outcomes

Primary

MeasureTime frameDescription
severity of labor pain by VASimmediately after interventionVisual Analog Scale: The scale features a 10-cm long vertical line, with 0 at the bottom end and 10 at the top end
Visual Similarity Scale for Fatigueimmediately after interventionThe scale consists of two subscales, fatigue and energy, and 18 items. There are 10 cm long horizontal lines with positive expressions at one end and negative expressions at the other end of the YİBGS. While the items of the fatigue subscale progress from positive to negative, the energy subscale has the opposite order. The lowest score obtained from the fatigue subscale is 0 and the highest score is 130. In the energy subscale, scores range from 0 to 50.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026