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Clinical Trials in Turkey / NCT07808840
Active, not recruiting Not applicable

Using Wet Towel During Labor

NCT07808840 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-08-25
Last updated
2026-09-09

Condition(s) studied

Labor PainComfortLabor Anxiety

Investigational drug(s) / intervention(s)

Wet Towel

Wet Towel: A woman who has entered the active phase and is being treated will be safely escorted to the bathroom and prepared for the procedure. A clean towel will be placed over the woman's head and shoulders, and water at an appropriate temperature (approximately 36-38°C) will be directed in a slow stream from the showerhead onto the towel. The water flow will be adjusted so that it gently touches the head area through the towel, and the procedure will be continued for at least 10 minutes. During this process, the woman will be continuously monitored, her comfort and safety will be ensured, and the fetal heart rate will be monitored in accordance with institutional protocol. After the procedure is completed, the woman's head and shoulders will be dried, and she will be taken back to her room for further assessment. Translated with DeepL.com (free version)

Study summary

The goal of this clinical trial is to learn whether the wet towel method applied during the first stage of labor can reduce labor pain and anxiety and improve childbirth comfort in first-time mothers. The main questions it aims to answer are:

Does the wet towel method reduce labor pain? Does the wet towel method improve childbirth comfort? Does the wet towel method reduce anxiety during labor?

Researchers will compare women who receive the wet towel method in addition to routine intrapartum care with women who receive routine intrapartum care alone to determine whether the intervention improves maternal outcomes during labor.

Participants will:

Be randomly assigned to either the wet towel intervention group or the routine care control group.

Receive the wet towel application for at least 10 minutes during the active phase of the first stage of labor or receive routine intrapartum care only.

Complete assessments of labor pain, childbirth comfort, and anxiety before and after the intervention using validated measurement tools

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
45 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Pregnant women admitted to the delivery room for childbirth * Pregnant women without any risks * Pregnant women with sufficient language proficiency to communicate effectively * Women experiencing their first pregnancy Exclusion Criteria: * Pregnant women admitted for a planned cesarean section * Pregnant women who do not agree to participate in the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sakarya Training and Research Hospital Adapazarı Sakarya

More Sakarya University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07808840 on ClinicalTrials.gov ↗ ← All trials in Turkey