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Labor PainNCT07808840

Using Wet Towel During Labor

A study testing Wet Towel in people with Labor Pain and Comfort, run by Sakarya University at 1 site in Turkey (Türkiye).

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 45 years, women onlyHealthy volunteers can take part
Conditions the study is for
Labor Pain, Comfort, Labor Anxiety
What is being tested?
Wet Towel
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteTurkey (Türkiye)
Study dates
25 Aug 2026to 30 Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 45 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • 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

Who cannot join

  • Pregnant women admitted for a planned cesarean section
  • Pregnant women who do not agree to participate in the study

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Sakarya Training and Research Hospital

    Adapazarı, Sakarya, 54050

Other trials in Turkey (Türkiye)

About this study

Official title: The Effect of Wet Towel Application During Labor on Labor Pain, Comfort, and Anxiety: A Randomized Controlled Study

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?

Read more

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

Read the detailed description

This randomized controlled trial aims to evaluate the effects of the wet towel method applied during the first stage of labor on labor pain, childbirth comfort, and anxiety levels among primiparous women. Labor pain and anxiety may negatively affect the childbirth experience, prolong labor, and reduce maternal comfort. Although several non-pharmacological methods have been shown to improve maternal outcomes during labor, evidence regarding the effectiveness of the wet towel method remains limited.

The study will be conducted at the Labor and Delivery Unit of Sakarya Training and Research Hospital. Sixty low-risk primiparous pregnant women will be randomly assigned to either an intervention group (wet towel application) or a control group receiving routine intrapartum care. In the intervention group, a clean towel will be placed over the woman's head and shoulders, and warm water (36-38°C) will be gently applied over the towel for at least 10 minutes during the active phase of labor. Participants in both groups will be assessed before and after the intervention.

Primary outcomes include labor pain, childbirth comfort, and anxiety during labor. Pain will be assessed using the Visual Analog Scale (VAS), comfort using the Childbirth Comfort Questionnaire, and anxiety using the Anxiety Assessment Scale for Pregnant Women in Labor. The findings of this study are expected to provide evidence regarding the effectiveness of the wet towel method as a simple, safe, low-cost, and non-pharmacological intervention to improve maternal comfort and reduce pain and anxiety during labor.

Being tested
Wet Towel
Keywords
Labor, Wet Towel Method, Vaginal Birth, Randomized Controlled Trial
Medical subject headings
Labor Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Wet TowelOther

    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 groups in NCT07808840
Study groupRoleWhat they receive
wet Towel groupExperimentalNot described
Receives: Other: Wet Towel
controlNo interventionNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pain intensity assessed by Visual Analog Scale (VAS)

    The primary outcome of this study is to evaluate the effect of wet towel application on labor pain intensity. Pain intensity will be assessed using the Visual Analog Scale (VAS) before and after the intervention.The primary outcome is labor pain intensity, assessed using the Visual Analog Scale before and after the intervention. Scores range from 0 to 10, with higher scores indicating greater labor pain intensity.

    Measured: Before intervention and immediately after intervention during the active phase of labor.

  2. Childbirth comfort level assessed by Childbirth Comfort Questionnaire

    The effect of wet towel application on childbirth comfort levels will be evaluated using the Childbirth Comfort Questionnaire before and after the intervention. Total scores range from 9 to 45, with higher scores indicating a higher level of childbirth comfort.

    Measured: Before intervention and immediately after intervention.

  3. Anxiety level during labor assessed by Anxiety Assessment Scale for Pregnant Women in Labor

    The effect of wet towel application on anxiety levels during labor will be evaluated. Anxiety level during labor will be assessed using the Scale for Assessing the Anxiety Status of Pregnant Women in Labor before and after the intervention. The mean score ranges from 1 to 5, with higher scores indicating higher levels of anxiety during labor.

    Measured: Before intervention and immediately after intervention.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Sep 2026
  2. Study start25 Aug 2026
  3. Primary completion30 Nov 2026 (estimated)
  4. Study completion30 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07808840
Sponsor's protocol ID
E-43012747-050.04-543-648
Status last verified
Sep 2026
First submitted
25 Aug 2026
Last updated
9 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data will not be shared because the data contain sensitive health information from pregnant women. To protect participant confidentiality and privacy, only aggregated results will be reported.

Publications

  • Shishido I, Konya I, Yano R. Effect on autonomic nervous activity of applying hot towels for 10 s to the back during bed baths. J Physiol Anthropol. 2020 Nov 19;39(1):35. doi: 10.1186/s40101-020-00245-7.

    PubMed 33213514
  • Mellado-Garcia E, Diaz-Rodriguez L, Cortes-Martin J, Sanchez-Garcia JC, Piqueras-Sola B, Macias JCH, Rivas Ruiz F, Rodriguez-Blanque R. Comparative Analysis of Therapeutic Showers and Bathtubs for Pain Management and Labor Outcomes-A Retrospective Cohort Study. J Clin Med. 2024 Jun 15;13(12):3517. doi: 10.3390/jcm13123517.

    PubMed 38930046
  • Taskin A, Ergin A. Effect of hot shower application on pain anxiety and comfort in the first stage of labor: A randomized controlled study. Health Care Women Int. 2022 May;43(5):431-447. doi: 10.1080/07399332.2021.1925282. Epub 2021 Jun 22.

    PubMed 34156915

Questions about this trial

What is this clinical trial studying?

A study testing Wet Towel in people with Labor Pain and Comfort, run by Sakarya University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 9 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pain intensity assessed by Visual Analog Scale (VAS) (time frame: Before intervention and immediately after intervention during the active phase of labor.). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07808840, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Sep 2026.

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