NCT05335681

Brief Summary

The use of non-pharmacological methods in labor pain is very important in order to improve the birth process, increase comfort and provide relaxation. The role of midwives, acting as patient advocate is to maintain comfort throughout the birth process. In order to do this, she should know very well the non-pharmacological methods to be applied to the pregnant woman and choose the most appropriate one. Applying a warm shower, which is one of the non-pharmacological methods; the uterus Increases perfusion, makes labor painless felt, increases the release of oxytocin, and decreases the release of stress hormones. In addition, while reducing the intervention rates, it improves birth and newborn outcomes and affects positively. Purpose of the research; labor pain of warm shower application, labor to evaluate the effect on satisfaction and birth outcomes.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
78

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2022

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2022

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

April 2, 2022

Completed
17 days until next milestone

First Posted

Study publicly available on registry

April 19, 2022

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 15, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 15, 2023

Completed
Last Updated

January 21, 2026

Status Verified

January 1, 2026

Enrollment Period

1 year

First QC Date

April 2, 2022

Last Update Submit

January 16, 2026

Conditions

Keywords

warm showerlabor painbirth Satisfactionhydrotherapymaternal health

Outcome Measures

Primary Outcomes (3)

  • Labor Pain

    Visual analog scale:On a 10 cm (100 mm.) ruler, which is marked painlessness on one end and the most severe pain possible on the other, the patient expresses his or her own pain by drawing a line, pointing or pointing. The length of the distance from the point where there is no pain to the point marked by the patient is measured in centimeters and the numerical value found shows the severity of the patient's pain.

    Baseline (Before the cervical dilation)

  • Labor pain

    Visual analog scale.On a 10 cm (100 mm.) ruler, which is marked painlessness on one end and the most severe pain possible on the other, the patient expresses his or her own pain by drawing a line, pointing or pointing. The length of the distance from the point where there is no pain to the point marked by the patient is measured in centimeters and the numerical value found shows the severity of the patient's pain.

    10 minutes after the cervical dilation

  • Labor pain

    Visual analog scale.On a 10 cm (100 mm.) ruler, which is marked painlessness on one end and the most severe pain possible on the other, the patient expresses his or her own pain by drawing a line, pointing or pointing. The length of the distance from the point where there is no pain to the point marked by the patient is measured in centimeters and the numerical value found shows the severity of the patient's pain.

    20 minutes after the cervical dilation

Secondary Outcomes (1)

  • Birth satisfaction

    Pregnant women in both groups will be visited by the researcher in the postpartum service within the first 24 hours postpartum and BSC will be applied.

Study Arms (2)

Warm Showers Application

EXPERIMENTAL

In the experimental group, a 20-minute warm shower (37 °C) will be administered when cervical dilation reaches at least 4 cm and again at 7 cm. The control group will receive standard care only. The hot shower will be applied to the sacral area, lower abdomen, and groin regions.

Behavioral: Warm Showers Application

Standard Intrapartum Care

NO INTERVENTION

No intervention will be provided to the control group. At the stages when cervical dilation reaches 4 cm and 7 cm, pain will be evaluated using the VAS at baseline, 10 and 20 minutes.

Interventions

In the experimental group, a 20-minute warm showers (37 °C) will be administered when cervical dilation reaches at least 4 cm and again at 7 cm. The control group will receive standard care only. The warm showers will be applied to the sacral area, lower abdomen, and groin regions. Throughout the intervention, the researcher will accompany the pregnant women to ensure safety and proper implementation of the procedure. Pain will be assessed using the VAS scale before the intervention and at 10 and 20 minutes after the intervention. The Birth Satisfaction Scale will be administered prior to discharge

Warm Showers Application

Eligibility Criteria

Age18 Years - 35 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsPregnant women who applied to the hospital for delivery
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Between the ages of 18 and 35,
  • Having a singleton fetus between 37-42 weeks of gestation,
  • Planning a a spontaneous vaginal birth,
  • Having a cervical dilatation \<5 cm.
  • Having a fetus weighing between 2500-4000 grams,

You may not qualify if:

  • Being short (\<145cm),
  • Being obese (BMI \>30),
  • Receiving pharmacological or non-pharmacological intervention for labor pain,
  • Having chronic diseases during pregnancy (gestational diabetes, hypertension, preeclampsia,
  • Undergoing operative vaginal delivery (forceps, vacuum),
  • Making an emergency cesarean decision,
  • Experiencing abnormal changes in fetal heart rates.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Öznur Hayat Öktem

Karabük, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Labor Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: randomized controlled
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Midwife, principal investigator

Study Record Dates

First Submitted

April 2, 2022

First Posted

April 19, 2022

Study Start

January 1, 2022

Primary Completion

January 15, 2023

Study Completion

January 15, 2023

Last Updated

January 21, 2026

Record last verified: 2026-01

Locations