Major Survey Findings of Listening to Mothers(SM) III: Pregnancy and Birth: Report of the Third National U.S. Survey of Women's Childbearing Experiences.
Eugene R Declercq, Carol Sakala, Maureen P Corry...
https://pubmed.ncbi.nlm.nih.gov/24453463/Actively Recruiting
Led by University of Zurich · Updated on 2026-05-14
74
Participants Needed
1
Research Sites
39 weeks
Total Duration
Researchers are studying pregnant women with non-insulin-dependent gestational diabetes to evaluate natural methods for ripening the cervix and preventing the need for medical induction of labor IOL. This trial aims to see if techniques like nipple stimulation and membrane sweeping can encourage spontaneous labor starting from 37 weeks of pregnancy, instead of scheduling IOL at 40 weeks as currently recommended by guidelines at the University Hospital Zurich. The study focuses on whether these natural methods can safely reduce the time to spontaneous labor and improve birth experiences. Participants are randomly assigned to one of two groups. The intervention group receives membrane sweeping twice weekly performed by medical staff, breast massage or nipple stimulation by the participant herself for 60 minutes three times per week, and colostrum harvesting starting at 36 weeks. The control group follows standard care, which includes colostrum harvesting twice daily beginning at 36 weeks but no membrane sweeping or breast massage. This outpatient approach allows comparison of natural cervical ripening methods with typical care. During the study, participants complete questionnaires about their experiences, adherence, and any side effects while the interventions occur. After delivery, satisfaction with the intervention or induction and overall birth experience are assessed. The main outcome measured is the time from 37 weeks until labor begins naturally. Researchers also track rates of spontaneous labor before IOL, use of oxytocin and pharmacological induction, hospitalization duration, postpartum bleeding, birth mode, and newborn health. The study follows participants through delivery to gather comprehensive data on safety and effectiveness.
CONDITIONS
Natural Cervical Ripening to Prevent Pharmacological Induction of Labor - a Pilot Study.
V
Verena Bossung, PD Dr. med.
N
Nicole Ochsenbein, Prof. Dr. med
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University of Zurich
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - From 36 weeks to onset of labor or planned induction at 40 weeks
Participants receive natural cervical ripening methods including membrane sweeping twice weekly by medical personnel from 37 weeks, and breast massage performed by the participant for 60 minutes on three days per week. Both intervention and control groups perform standard colostrum harvesting starting at 36 weeks.
Twice weekly membrane sweeping visits and breast massage performed by participants three days per week
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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https://pubmed.ncbi.nlm.nih.gov/27914274/University of Zurich
Lead Sponsor