The Effect of Acupressure in Non-breastfeeding Mothers After Preterm Cesarean Delivery
Sponsored by Esra SARI
About this trial
Last updated 5 years ago
Study ID
ESARI
Status
Unknown status
Type
Interventional
Phase
N/A
Placebo
No
Accepting
18 to 35 Years
Female
Not accepting
Healthy Volunteers
Trial Timing
Ended 5 years ago
What is this trial about?
The effect of acupressure in non-breastfeeding mothers after preterm cesarean delivery
What are the participation requirements?
Inclusion Criteria
- Mothers between the ages of 19-35,
- Mothers who gave birth by cesarean operation,
- Mothers who gave birth before 37th week of pregnancy,
- Primiparous mothers,
- Mothers whose baby is lying in NICU,
- Mothers who do not have any chronic diseases,
- Mothers who do not use breast milk enhancing drugs, vitamins and supplements,
- Mothers who do not have any anotomic disorder in the breast,
- Mothers who cannot breastfeed,
- Mothers who do not have any injured skin, fracture, swelling or muscle pain, especially in the little finger.
- Mothers without literacy problems, mental disabilities and communication problems,
- Mothers living within the borders of the province of Van,
- Mothers who agree to participate in the study.
Exclusion Criteria
- Mothers of premature newborns who cannot be fed breast milk,
- Mothers who are multiparous,
- Mothers with chronic disease,
- Mothers who have a condition preventing milking,
- Mothers whose language is insufficient in understanding and speaking Turkish,
- Mothers who have breast abscess problems,
- Mothers who have babies with congenital anomalies,
- They are mothers who do not volunteer to participate in the study
Locations
Location
Status
Recruiting