Effects of Warm Shower on Lactation, Fatigue, and Maternal Burnout
WARM-SHOWER
The Effect Of Warm Showers On Exhaustıon, Fatigue, Lactation Onset Symptoms and Breast Milk Quantity In The First Three Postpartum Days: A Randomized Controlled Trial
1 other identifier
interventional
64
1 country
1
Brief Summary
Lactation is a physiological process in which various hormones, especially prolactin and oxytocin, play a role. Methods such as warm showers are preferred because they are easy to apply and have a quick effect, as well as being cost-effective. It increases the amount of milk by showing a direct effect on oxytocin and prolactin hormones in the breastfeeding process that strengthens the bond between mother and baby. It helps to make the breastfeeding process more enjoyable for mother and baby. Guidelines in the literature emphasize that the mother should be psychologically evaluated and that practices that can relax her according to her needs should be applied to increase breastfeeding success. In addition to hormonal regulation, a warm shower improves self-care. In this way, breastfeeding motivation increases. The aim of this study was to investigate the effect of warm showers in the morning and evening in the first 3 postpartum days on the amount of breast milk by shedding light on hormones and lactation process.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2025
Shorter than P25 for not_applicable
1 active site
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
October 10, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 10, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
June 15, 2026
CompletedFirst Submitted
Initial submission to the registry
June 19, 2026
CompletedFirst Posted
Study publicly available on registry
July 10, 2026
CompletedJuly 10, 2026
June 1, 2026
6 months
June 19, 2026
July 4, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Maternal Burnout
Maternal Burnout Scale (MBS). The Maternal Burnout Scale was used to assess maternal burnout levels. The scale consists of 15 items rated on a 4-point Likert scale and includes the dimensions of physical and emotional exhaustion, emotional distancing from the child, and reduced maternal accomplishment. Higher scores indicate higher levels of maternal burnout.
Assessed at baseline (6-12 hours postpartum), immediately after the intervention, and at 24, 48, and 72 hours postpartum, as well as on postpartum days 7 and 14.
Lactation Onset Indicators
Lactation onset indicators will be assessed as a composite outcome using the Lactation Assessment Form, which includes breast fullness, milk secretion characteristics, and post-feeding breast status.
Assessed at baseline (6-12 hours postpartum), immediately after the intervention, and at 24, 48, and 72 hours postpartum, as well as on postpartum days 7 and 14.
Postpartum Fatigue
Postpartum fatigue will be assessed using the Visual Analogue Scale for Fatigue (VAS-F), an 18-item instrument designed to assess fatigue. Higher scores indicate greater postpartum fatigue.
Assessed at baseline (6-12 hours postpartum), immediately after the intervention, and at 24, 48, and 72 hours postpartum, as well as on postpartum days 7 and 14.
Infant breast milk intake score
Infant breast milk intake will be assessed using the IMDAT Breast Milk Intake Scoring System. Higher scores indicate greater breast milk intake. Unit of
Assessed at baseline (6-12 hours postpartum), immediately after the intervention, at 24, 48, and 72 hours postpartum, and on postpartum days 7 and 14.
Study Arms (2)
Warm Shower + Routine Postpartum Care
EXPERIMENTALParticipants receive routine postpartum care plus a standardized warm shower intervention during the first three postpartum days. Women in the intervention group are instructed to take a warm shower (37-39°C) once daily for 10-15 minutes following confirmation of clinical stability and mobilization readiness. The intervention is delivered in addition to routine postpartum care and is intended to promote relaxation, physical comfort, maternal well-being, and lactation-related outcomes during the early postpartum period.
Routine Postpartum Care (Control)
NO INTERVENTIONParticipants in the control group receive routine postpartum care according to hospital protocol, including standard maternal and newborn monitoring, breastfeeding support, and postpartum recovery care. No warm shower intervention is administered.
Interventions
Participants receive routine postpartum care in addition to a standardized warm shower (37-39°C, 10-15 minutes) once daily during the first three postpartum days after cesarean birth.
Eligibility Criteria
You may qualify if:
- Having given birth between 37 and 42 weeks of gestation
- Having had a cesarean delivery
- Being a primipara
- Being admitted to the postpartum ward within the first 6 hours
- No physical or cognitive limitations preventing the ability to shower
- Providing written informed consent
You may not qualify if:
- Premature infant or infant in the neonatal intensive care unit
- Maternal history of infection, complications, or psychiatric diagnosis
- Physiological condition preventing breastfeeding
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
KTO Karatay University
Konya, Karatay, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assoc.Prof.
Study Record Dates
First Submitted
June 19, 2026
First Posted
July 10, 2026
Study Start
October 10, 2025
Primary Completion
April 10, 2026
Study Completion
June 15, 2026
Last Updated
July 10, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will not share