Showering During Labor

July 5, 2023 updated by: Yasemin Hamlaci Baskaya, Sakarya University

The Effect of Showering During Labor on Perceived Labor Pain, Parenting Behavior and Birth Memory

The research covers the birth memory evaluation to determine the pregnancy process, the labor process and the changes in the perceived pain level during this process, the parenting behavior immediately after the birth and the process of the birth.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

The Effect of Showering During Labor on Perceived Birth Pain, Parenting Behavior and Birth Memory Labor is a natural process in which the fetus and its appendages, which are the product of pregnancy, are expelled from the uterus approximately 40 weeks after the last menstrual bleeding. Birth is a very meaningful and unique experience for the pregnant woman and her family. Although it results in a positive experience, they are faced with serious pain, discomfort and sensory situations that will force them in this process. This pain is a severe acute pain and differs from other types of pain due to the fact that it is a part of a natural process, experienced in a limited time and mother-infant relationship. In the literature, labor pain can be relieved by two methods: pharmacological (drugs) and non-pharmacological (non-drug methods). In the guide published by the World Health Organization (WHO) in 2018, non-pharmacological methods are recommended to be used as they are more reliable and less invasive. Non-pharmacological methods are generally simple, reliable for mother-baby health, easy to use, accessible, economical and do not require special training. The application of non-pharmacological methods can be safely applied by midwives independently, as it does not require a physician's request and has minimal side effects. The midwife, who decides with the pregnant woman the non-pharmacological method to be used in the management of labor pain, can apply this method with her own autonomy and ensure that the mother has a more comfortable birth process. Non-pharmacological methods include hot/warm bath, hydrotherapy, hot-cold application, movement, positions, breathing, relaxation exercises, acupuncture, TENS, yoga, massage, aromatherapy, music, hypnosis. These practices increase the comfort of the pregnant woman during the labor process, relieve the level of pain and provide a positive birth experience and positive progress in the mother-baby interaction. One of the non-pharmacological methods used to reduce labor pain is hydrotherapy/warm application. Although there is not enough evidence about the history of Hydrotherapy/Hot treatment, it was reported that the spa waters of Hippocrates had a therapeutic effect in the fifth century. The use of water in childbirth and labor started with Igor Charkovsky in Russia in 1970, and then it was spread in Europe under the leadership of Micheal Odent. Hot application causes vasodilation in peripheral blood vessels, oxygenation of the region, nutrition, removal of waste materials, and relaxation is experienced by reducing tension in the muscles. In addition, the feeling of pain decreases. As a result, fetal well-being increases. The positive outcome of the birth process as a result of a healthy and beautiful progress also affects the understanding of mother-infant interaction and parenting behavior in the postpartum period. Postnatal parenting behavior is the behavior of the mother showing that she is interested in the newborn baby, such as taking care of the newborn in the postpartum period, asking questions about it, smiling at the newborn baby or making sounds. It can be affected by various factors, the situations experienced during labor and the past experiences of himself/herself. In a randomized controlled study conducted by Tuncay (2016), it was determined that the postpartum parenting behavior scale average score of the pregnants in the experimental group who received hydrotherapy was higher, and in other words, the pregnants in the experimental group behaved more positively towards the newborns in the postpartum period (p=0.001). Birth also affects memory. A pregnant woman who has experienced a difficult and long labor in the past is more anxious and fearful. However, past experiences do not always have this effect on women. Positive experiences with pain lead to correct behavior and positive changes. The experience experienced with the birth of each child is different and has the potential to change a woman's life in every sense. In order to protect the psychological health of the woman in the postpartum period, it is expected that her memories of the birth will be positive in her mind and that she will feel positive emotions when she remembers her birth. However, some women experience birth as a traumatic event rather than a positive and happy event. Some may describe this process as negative, while others may see it as a normal process. In the literature review, it has been determined that there are not enough studies on birth memory in Turkey. As a result, it is stated in the studies that non-pharmacological methods such as warm shower application may be effective in the positive outcome of labor, ensuring mother-infant interaction, acquiring parenting behavior and positive recall of labor in the future. For this purpose, the study was planned to evaluate the effect of warm shower applied during labor on women's pain levels, postpartum parenting behavior and birth memory.

Study Type

Interventional

Enrollment (Actual)

81

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

    • Kocaeli
      • Sakarya, Kocaeli, Turkey
        • Sakarya Training and Research Hospital

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

18 years to 45 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Being able to communicate verbally
  • Between 18 - 45 years old,
  • Being Primiparous/Nulliparous,
  • Term pregnancy (38-41 weeks of pregnancy),
  • Being in the latent and active phase of labor (Cervical dilation 4-5 cm and 7-8 cm)
  • Having a single fetus
  • Fetus in vertex presentation,
  • Low risk pregnancy and no complications (EMR, Placenta Previa, HT, DM etc.),
  • No obstetric risk (diabetes, pre-eclampsia, premature birth threat, etc.)
  • Not having had any surgery in the spinal region,
  • Volunteer to participate in the research

Exclusion Criteria:

  • Not being willing to participate in the study,
  • Not being open to communication and cooperation,
  • Presence of hearing-sight and mental problems that would prevent the research,
  • Be younger than 18 years old, over 45 years old,
  • Being multiparous
  • Being outside 38-41 weeks of gestation
  • Being in the transitional phase of birth,
  • Not planning a vaginal birth,
  • Decision of cesarean delivery during labor,
  • Presence of any medical or obstetric risk factors (fetal distress, prolonged labor, etc.)

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
No Intervention: Control group
Women in the control group will not be interfered with and will be followed in line with the routine follow-up protocol of the clinic.
Experimental: Experimental group
The women in this group will have a warm shower during the labor process.
A warm shower will be applied for 20 minutes to the pregnant woman whose cervical dilatation reaches 4-5 cm and 7-8 cm.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perceived pain level
Time Frame: 6 hours
When cervical dilation is 4-5 cm and 7-8 cm, perceived labor pain will be defined by the visual pain scale.
6 hours
Birth Memories and Recall Questionnaire
Time Frame: 6 hours
It will be determined how taking a shower during labor will affect the birth memory.
6 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postpartum Parenting Behavior Scale
Time Frame: 1 hours
It will be determined whether taking a shower during labor affects parenting behavior.
1 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 1, 2022

Primary Completion (Actual)

March 31, 2023

Study Completion (Actual)

July 4, 2023

Study Registration Dates

First Submitted

August 31, 2022

First Submitted That Met QC Criteria

September 3, 2022

First Posted (Actual)

September 7, 2022

Study Record Updates

Last Update Posted (Actual)

July 7, 2023

Last Update Submitted That Met QC Criteria

July 5, 2023

Last Verified

July 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 26082022

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The follow-up of the study data will be provided by both researchers.

IPD Sharing Time Frame

The data will be kept by the researchers until the study is reported. After the study is published, it will contribute to the literature.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • CSR

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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