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Showering During Labor

Effects of Showering During Labor on Pain, Anxiety, Comfort, Satisfaction, and Labor Outcomes: A Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07571785
Enrollment
94
Registered
2026-05-06
Start date
2022-03-01
Completion date
2022-08-30
Last updated
2026-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Childbirth, Labor

Brief 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.

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.

Sponsors

Nilgun Avci
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
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

* 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

Design outcomes

Primary

MeasureTime frameDescription
Labor Pain IntensityEvery 2 hours during labor (up to 8 hours) and immediately before and after each shower session during the same labor admission.Pain intensity assessed using the Visual Analog Scale (VAS) during labor.

Secondary

MeasureTime frameDescription
Anxiety Level During LaborEvery 2 hours during labor (up to 8 hours) and immediately before and after each shower session during the same labor admission.Anxiety assessed using the Visual Analog Scale (VAS) during labor.
Maternal Comfort During LaborAt 10 minutes after the first shower session during active laborMaternal comfort assessed using the Childbirth Comfort Questionnaire.
Birth Satisfaction2 hours postpartum.Birth satisfaction assessed using the Birth Satisfaction Scale.
Duration of LaborFrom admission to the labor unit until delivery.Total duration of labor measured in hours, obtained from clinical records.
Mode of DeliveryAt delivery.Type of delivery (vaginal or cesarean) recorded from clinical records.
Use of Obstetric InterventionsDuring labor and recorded at delivery.Use of obstetric interventions (e.g., induction, augmentation, episiotomy) recorded from clinical records.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 7, 2026