- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06660615
The Effect of Continuous Midwifery-led Care in Birth Management
February 20, 2025 updated by: Betul Uncu, Istanbul University - Cerrahpasa
The Effect of Midwife-Led Care on Perception of Labour Pain, Duration of Labour, Comfort of Labour and Respectful Maternity Care: a Single Blinded Randomised Controlled Trial
Caesarean section is an emergency procedure necessary to prevent harm or death to the mother or newborn.
Worldwide, caesarean section rates are steadily increasing.
This increase not only has negative consequences on maternal and child health, but also leads to a reduction in essential resources and impedes access to health services worldwide.
The International Federation of Gynaecology and Obstetrics (FIGO) has called for help from government bodies, professional organisations, women's groups and other stakeholders to reduce unnecessary caesarean sections.
According to a review of antenatal and intrapartum interventions to reduce caesarean section, promote vaginal birth and reduce fear of childbirth; the importance of support in the intrapartum period is prominent.
The National Institute for Health and Care Excellence (NICE) states that this support with a midwife who provides care and one-to-one support to the woman in labour reduces women's anxiety and increases their sense of trust.
Study Overview
Detailed Description
Vaginal delivery of low-risk pregnancies is best provided and guided by a midwife.
It is seen that receiving support from a midwife in the birth of low-risk pregnancies does not increase the risks for the mother or newborn and has many economic and emotional advantages.
The World Health Organisation recommends respectful care based on woman-centred care in the intapartum period for a positive birth experience.
Respectful Maternity Care has been recognised as a key strategy to improve the quality of maternity care.
Although there is no clear consensus on the definition of respectful maternity care, it is generally considered synonymous with intimate and woman-centred care.
It is a care approach that emphasises the fundamental rights of women, newborns and families and increases adequate access to evidence-based care while recognising their needs and preferences.
In this direction, midwives are expected to add respectful maternity care to their clinical skills in the management of the birth process.
In the literature, it is seen that respectful and helpful interaction between women and health professionals during labour creates positive perceptions in women.
In the study of Liu et al. (2021), it is stated that midwife-led management of labour leads to the formation of positive perceptions in women.
Fear of labour, labour pain and duration of labour in midwife-led care on the behaviour of the students in the study.
Study Type
Interventional
Enrollment (Actual)
85
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Mardin, Turkey
- Mardin Nusaybi̇N State Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Pregnant women with spontaneous pregnancy between 38-42 weeks of gestation
- single fetus head presentation
- first pregnancy
- without any pregnancy-related risk status (such as preeclampsia, gestational diabetes)
- who were admitted to the delivery room for normal labour will be included in the study.
Exclusion Criteria:
- WOMEN WHO CANNOT GIVE BIRTH NORMALLY
- WANT TO LEAVE THE LABOUR FORCE
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Receiving midwife-led care
The birth process will be followed by the same midwife from the beginning of the intrapartum period until the birth of the baby and placenta.
In this process, positive respectful maternal care will be included in line with the recommendations of WHO (İsbir & Sercekuş, 2017).
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The birth process will be followed by the same midwife from the beginning of the intrapartum period until the birth of the baby and placenta.
In this process, positive respectful maternal care will be included in line with the recommendations of WHO (İsbir & Sercekuş, 2017).
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No Intervention: Midwife-Led Non-Care Receiving Care
Participants in the group will receive routine care normally provided only in the hospital.
Within this care, from the beginning of the intrapartum period until the birth of the baby and placenta, the birth process will be followed under the supervision of a midwife or physician who is randomly available within the working conditions of the birth unit.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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The Effect of Midwife-Led Care on Perception of Labour Pain, Duration of Labour, Comfort of Birth and Respectful Maternity Care
Time Frame: 1 years
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Measurement Tools Information Form (IF) (Appendix 1): This form was prepared in line with the literature (Liu et al., 2021) and includes socio-demographic and obstetric characteristics of the participants.
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1 years
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Birth Pain
Time Frame: 1 years
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Visual Analog Scale (VAS) (ANNEX-2): The Visual Analog Scale (VAS) was developed by Price et al. in 1983 and is used to measure pain intensity and for pain monitoring.
The VAS is 10 cm long and the two ends are named differently.
On the scale, '0' indicates no pain and '10' indicates the most severe level of pain.
The VAS is a measurement tool that is frequently and reliably used to assess labor pain (Price et al., 1983; Mutlu & Özkaya, 2021).
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1 years
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birth monitoring
Time Frame: 1 years
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Birth Monitoring Form (DIF) (ANNEX-3) : It was aimed to evaluate the labour process with the labour monitoring form developed by the researchers.
In the birth follow-up form, data obtained from pregnant women in G1 and G2 regarding cervical dilatation and dilatation, duration, frequency and intensity of contractions, time of delivery, and time of placental separation will be recorded.
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1 years
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Comfort of Birth
Time Frame: 1 years
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Birth Comfort Scale (BCS) (ANNEX-4): It was developed by Kerri Durnell Schuiling in 2003, inspired by Kolcaba's comfort theory.
The original version consists of fourteen items.
The scale is a five-point Likert-type scale (1= Strongly disagree, 5= Strongly agree).
Its Turkish validity and reliability was performed by Potur et al.
There are three subscales/factors (environmental, physical, psychospiritual) in the Turkish version of the comfort of labour scale consisting of nine items.
Items 2,3,4,6 of the scale are divided into sub-dimensions in the physical dimension, items 7,8 in the psychospiritual dimension and items 1,5,9 in the environmental dimension.
A minimum of 9 and a maximum of 45 points can be obtained from the scale.
The Cronbach Alpha value of the scale was found to be 0.75 (Potur et al., 2015).
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1 years
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Respectful Maternity Care
Time Frame: 1 years
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Respectful Motherhood Care Scale (RMCS) (ANNEX-5): The scale was developed by Dişsiz et al. in 2023.
With the five-point Likert-type scale, it was aimed to evaluate the respectful maternity care perceived by women between the 6th week and 1 year postpartum during pregnancy, birth and postpartum period.
The scale consists of a total of 29 items and 3 sub-dimensions with mixed positive and negative statements.
The sub-dimensions are 'Consensual Dignified Care (17 items)', 'Psychological Abuse and Care Neglect (7 items)' and 'Physical Violence, Privacy Violation and Discrimination (5 items)'.
The highest total score that can be obtained from the scale is 145 and the lowest score is 29.
An increase in the score obtained from the overall scale indicates that the woman's perception that she received respectful maternity care during pregnancy, birth and postpartum period increased, while a decrease indicates that the woman's perception that she received respectful maternity care during pregn
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1 years
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 17, 2024
Primary Completion (Actual)
February 20, 2025
Study Completion (Actual)
February 20, 2025
Study Registration Dates
First Submitted
October 17, 2024
First Submitted That Met QC Criteria
October 24, 2024
First Posted (Actual)
October 28, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 20, 2025
Last Verified
October 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023/1191
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
I'm not sure right now.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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