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Effect of Maryam Plant and Surah on Birth Pain, Anxiety and Satisfaction

Effect of Maryam Plant and Surah on Birth Pain, Anxiety and Satisfaction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07175337
Enrollment
125
Registered
2025-09-16
Start date
2023-09-06
Completion date
2025-08-20
Last updated
2025-09-16

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

Conditions

Cervical Dilatation of 4-6 cm (Early Active Phase), Muslim, No Pregnancy Complications, Pregnancy

Keywords

Virgin Mary's Hand Plant, Surah Maryam, Labor Pain, Birth Anxiety, Birth Satisfaction

Brief summary

This randomized controlled trial was conducted to determine the effects of spiritual support provided by Virgin Mary's hand plant and Surah Maryam on labor anxiety, labor pain, and satisfaction.

Detailed description

No other study has been found investigating the effects of both the Maryam Surah and the Virgin Mary plant on labor anxiety, labor pain, and labor satisfaction. The effects of the parameters to be examined in this project have not yet been examined, and the effects of the Maryam Surah recited to pregnant women during labor and the Virgin Mary plant, believed to help open the birth canal, have not been tested. The study aims to contribute to the literature through a randomized controlled trial and to obtain data that will inform future studies.

Interventions

BEHAVIORALSurah Maryam group

Pregnant women who came for birth were taught Surah Maryam. They were monitored throughout the labor process, and in addition to routine midwifery care, Surah Maryam was played twice during labor to provide spiritual support.

BEHAVIORALVirgin Mary's Hand Plant Group

he pregnant woman was monitored throughout labor; in addition to routine midwifery care, she was given spiritual support by placing the Virgin Mary's Hand plant in water and watching the plant unfold, encouraging her to believe that the birth canal also opens in the same way.

Sponsors

Ataturk University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

The research was conducted in a randomized controlled experimental design.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* • Being literate * Being open to communication * Being at term (37-40 weeks) * Having a single, live fetus * Having no pregnancy complications * Having no conditions preventing labor * Having 4-6 cm cervical dilation (early active phase) * Planning a vaginal birth * Not having a diagnosed psychiatric illness * Volunteering to participate in the study * Being in cephalic presentation * Being Muslim

Exclusion criteria

* Being illiterate * Having a high-risk pregnancy * Having a planned cesarean section * Developing complications during labor * Using pain-reducing methods such as narcotic analgesics or sedatives * Having a diagnosed psychiatric illness

Design outcomes

Primary

MeasureTime frameDescription
Visual Analog Scalethrough study completion, an average of 1 yearVAS is used to measure perceived pain. It consists of a 10 cm (100 mm) line with one end labeled no pain and the other worst possible pain. The participant marks a point on the line corresponding to the intensity of their pain. The distance in millimeters from no pain to the mark is measured and recorded as the pain score. Cline et al. (1992) reported that vertical orientation was better understood by patients. The scale was originally developed by Price et al. (1983). Eti-Aslan (1998) found that VAS was more sensitive in the evaluation of postoperative (acute) pain
Oxford Worry About Labour Scale (OWLS)Through study completion, an average of 1 yearDeveloped by Redshaw, Martin, Rowe, and Hockley (2009) to assess women's worries related to the childbirth process. The Turkish validity and reliability study was conducted by Erkal and Özentürk (2016). The scale consists of 10 items rated on a 4-point Likert scale: (1) Very worried, (2) Fairly worried, (3) Not very worried, (4) Not at all worried. Scores are calculated from the total (minimum = 10, maximum = 40). The scale has three subdimensions: Pain and Distress, Uncertainty Before Birth, and Interventions. The Cronbach's alpha reliability coefficient of the Turkish version was found to be 0.83 (Erkal Aksoy & Özentürk, 2016). In this study, the Cronbach's alpha value of the questionnaire was found to be 0.75.
Birth Satisfaction Scale-Revised (BSS-R)through study completion, an average of 1 yearThe original Birth Satisfaction Scale was developed by Martin and Fleming (2011) to assess women's satisfaction with childbirth. In 2013, Martin and Martin revised the scale by reducing the number of items, resulting in the Birth Satisfaction Scale-Revised (BSS-R). The BSS-R is a 10-item Likert-type scale rated as: Strongly agree (4 points), Agree (3 points), Neutral (2 points), Disagree (1 point), Strongly disagree (0 points). Items 2, 4, 7, and 8 are reverse-scored. The total score ranges from 0 to 40, with higher scores indicating greater satisfaction. The scale has three subdimensions: Quality of Care (communication, support from healthcare providers, and cleanliness of the delivery room), Women's Personal Attributes (sense of control and anxiety during childbirth), and Stress Experienced During Labor (perceived stress and duration of labor). The Cronbach's alpha reliability coefficient of the Turkish version was reported as 0.72 (Gökmen, 2017). In this study, the Cronbach's alpha

Countries

Turkey (Türkiye)

Outcome results

None listed

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