CClinicalTrials.gg
CompletedNCT07571785Updated May 6, 2026

Showering During Labor

An interventional study of Showering During Labor in Labor and Childbirth, sponsored by Nilgun Avci. Completed at 1 site in Turkey (Türkiye). Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-06.

Sponsored by Nilgun Avci · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 3 years 11 months after the study started (first participant enrolled Mar 2022, registered Feb 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
94
Allocation
Randomized
Ages
18 Years and older
Sex
Female
01

Study summary

This study examined whether showering during labor affects pain, anxiety, comfort, satisfaction, and labor outcomes in women undergoing vaginal birth. Non-pharmacological methods are commonly used to support women during labor, and warm showering may help reduce discomfort and emotional distress during the labor process.

In this randomized controlled trial, pregnant women in active labor were assigned either to a shower group or to a control group receiving routine labor care. Women in the shower group were allowed to shower during labor under standardized conditions, while the control group received routine intrapartum care without showering. Pain and anxiety levels were assessed repeatedly during labor, while comfort and birth satisfaction were evaluated during and after birth using validated measurement tools.

The results of this study aim to contribute to evidence-based intrapartum care practices by evaluating the role of showering as a supportive intervention during labor.

02

Conditions studied

  • Labor
  • Childbirth
03

In context

Lead sponsor

Nilgun Avci is the lead sponsor of 5 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Women admitted to the labor unit during the study period
  • Term pregnancy (37-41 weeks)
  • Planned vaginal birth
  • Cervical dilation greater than 5 cm
  • Volunteered to participate and provided informed consent

Exclusion criteria

Exclusion Criteria:

  • Inability to communicate in Turkish
  • Hearing or mental health conditions
  • Conversion from vaginal birth to cesarean section
  • Age under 18 years
  • High-risk pregnancy (e.g., preeclampsia, diabetes, hypertension, multiple pregnancy, placental abnormalities)
  • Use of epidural anesthesia
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
94 participants (actual)

Study arms

  • Experimental
    Shower During Labor

    Participants were allowed to shower during active labor (cervical dilation \>5 cm) in a private bathroom within the labor room. Showering was permitted at the participant's preference, for at least 20 minutes per session, with water temperature maintained between 35-40°C. Safety measures were implemented, including accompaniment by a companion or researcher.

    Behavioral: Showering During Labor

  • No intervention
    Control: Routine Labor Care

    Participants received routine intrapartum care without showering during labor.

Interventions

  • BehavioralShowering During Labor

    Participants were allowed to shower during active labor (cervical dilation \>5 cm) in a private bathroom within the labor room. Showering was permitted at the participant's preference, for at least 20 minutes per session, with water temperature maintained between 35-40°C. Safety measures were implemented, including accompaniment by a companion or researcher.

06

What researchers measure

Primary outcomes

  1. Labor Pain Intensity

    Pain intensity assessed using the Visual Analog Scale (VAS) during labor.

    Time frame: Every 2 hours during labor (up to 8 hours) and immediately before and after each shower session during the same labor admission.

Secondary outcomes

  1. Anxiety Level During Labor

    Anxiety assessed using the Visual Analog Scale (VAS) during labor.

    Time frame: Every 2 hours during labor (up to 8 hours) and immediately before and after each shower session during the same labor admission.

  2. Maternal Comfort During Labor

    Maternal comfort assessed using the Childbirth Comfort Questionnaire.

    Time frame: At 10 minutes after the first shower session during active labor

  3. Birth Satisfaction

    Birth satisfaction assessed using the Birth Satisfaction Scale.

    Time frame: 2 hours postpartum.

  4. Duration of Labor

    Total duration of labor measured in hours, obtained from clinical records.

    Time frame: From admission to the labor unit until delivery.

  5. Mode of Delivery

    Type of delivery (vaginal or cesarean) recorded from clinical records.

    Time frame: At delivery.

  6. Use of Obstetric Interventions

    Use of obstetric interventions (e.g., induction, augmentation, episiotomy) recorded from clinical records.

    Time frame: During labor and recorded at delivery.

07

Study locations

1 site
  • State Obstetrics and Gynecology Hospital, Istanbul
    Istanbul, Istanbul 34010, Turkey (Türkiye)
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07571785
Lead sponsor
Nilgun Avci
Responsible party
Nilgun Avci (phD, Biruni University) — Sponsor-investigator
First posted
May 6, 2026
Start date
Mar 1, 2022
Primary completion
Aug 30, 2022
Completion
Aug 30, 2022
Last update
May 6, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

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