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Clinical Trials in Turkey / NCT07447609
Recruiting Not applicable

THE EFFECT OF REIKI ON BREASTFEEDING, PAIN AND COMFORT AFTER CESAREAN SECTION

NCT07447609 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-01-15
Last updated
2026-03-03

Condition(s) studied

Postpartum ComfortPostpartum CareCesarean Section PainBreastfeeding Self-EfficacyPerceived Insufficient Milk SupplyReikiReiki TherapyPostpartum Pain

Investigational drug(s) / intervention(s)

reikisham reiki

reiki: The effect of Reiki practice on breastfeeding during the postpartum period has not been evaluated; it is considered unique because it is evaluated together with its effect on pain and comfort, and offers a holistic approach to support care for women in the postpartum period.

sham reiki: It is believed that adding a sham reiki group alongside postpartum reiki treatment will increase the reliability and originality of the study.

Study summary

EFFECT OF REİKİ APPLİED DURİNG THE POSTPARTUM PERİOD ON BREASTFEEDİNG, PAİN, AND COMFORT IN WOMEN WHO DELİVERED BY CESAREAN SECTİON

The aim of this randomized controlled trial is to determine the effect of Reiki applied to volunteer women after cesarean section on breastfeeding, pain, and comfort in the postpartum period. The main questions it aims to answer are:

Is there a difference in postpartum breastfeeding, pain, and comfort between the group receiving Reiki and the group receiving standard care? Is there a difference in postpartum breastfeeding, pain, and comfort between the group receiving Reiki and the group receiving Sham Reiki? Participants will receive Reiki six times postpartum: three times one-on-one during their hospital stay, and remotely in the second, third, and fourth weeks. The control group will receive standard care. The Sham Reiki group will receive Reiki points applied by a person without Reiki knowledge.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
45 Years
Healthy volunteers
No
Inclusion Criteria: * Mothers aged 18 and over, * Literate in Turkish, * Non-smoker, non-drug user, * Gave birth by cesarean section at term, * Baby with them after birth, * Not using any breast milk-increasing medication, vitamins, or supplements, * Baby's birth weight between 2500-4000 grams, * Baby's Apgar score at least seven points at 1 and 5 minutes, * Having had a cesarean section under spinal anesthesia, * Those who agree to participate in the study. Exclusion Criteria: * Preeclampsia/eclampsia, active postpartum hemorrhage, sepsis/fever ≥38°C, * Need for intensive care, * Birth before 37 weeks, * Serious neonatal problems, * Baby arriving at the ward after mother (follow-up in neonatal intensive care unit without hospitalization after birth), * Excessive sedation due to analgesia, * Communication difficulties, * Markedly negative attitude towards Reiki.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Samsun Sehir Hastanesi Samsun Turkey (Türkiye) Recruiting

More Saglik Bilimleri Universitesi trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07447609 on ClinicalTrials.gov ↗ ← All trials in Turkey