Effects of Warm Shower on Lactation, Fatigue, and Maternal Burnout

NCT07694856 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 64

Last updated 2026-07-10

No results posted yet for this study

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.

Conditions

  • Maternal Burnout
  • Postpartum Fatigue
  • Breastfeeding

Interventions

BEHAVIORAL

Warm Shower

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.

Sponsors & Collaborators

  • KTO Karatay University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-10-10
Primary Completion
2026-04-10
Completion
2026-06-15

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07694856 on ClinicalTrials.gov