Effects of massage techniques on breastfeeding and maternal well-being after cesarean delivery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the impact of two non-pharmacological interventions, oxytocin massage and reflexology, on mothers who have undergone cesarean sections. It aims to address issues such as insufficient milk perception, breastfeeding motivation, fatigue, and anxiety in the postpartum period. By comparing these interventions to a control group, the study seeks to determine their effectiveness in enhancing maternal health and promoting breastfeeding. The research is particularly relevant given the high cesarean section rates in Turkey and the associated challenges faced by new mothers.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Mothers who gave birth at the age of 18 and over
* The one who is married
* At least primary school graduate,
* Primiparous mothers who gave birth by cesarean section,
* Having a single, healthy newborn at full term,
* Those who did not experience any problems during pregnancy and the early postpartum period,
* The tissue integrity in the area to be applied is complete and healthy,
* Breastfeeding her baby after birth,
* The baby is healthy, has no problems with the sucking reflex and does not have any congenital anomalies,
* Women who agree to participate in the research will be included in the study.

Exclusion Criteria:

* Those who gave birth by cesarean section before the 37th week of pregnancy,
* Women who gave birth by cesarean section with combined anesthesia,
* Discharged before 36 hours after birth,
* Having chronic diseases such as heart disease, diabetes, hypertension,
* Those with infectious diseases, infections, open wounds, masses, fractures, dislocations, deformities, varicose veins, burns, eczema, hematomas, thrombophlebitis, deep vein thrombosis on the foot skin,
* Experiencing any postpartum complications,
* Their baby is not with their mother for any reason,
* Those who have received a psychiatric diagnosis such as anxiety and depression,
* Women who want to leave the research at any stage of the research

Where it's running

• Büşra Nur GELDİ
  Giresun, Turkey (Türkiye) Recruiting

Study contacts

• Principal investigator: Büşra Nur GELDİ — Ordu University
• Study coordinator: Büşra Nur GELDİ
• Email: busranurgeldi@gmail.com
• Phone: +905344313248

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.