About this trial
Our study aims to determine the effect of pregnant-controlled automatic sacral massage on mothers' labor pain, perception, process and midwives' satisfaction. The research was planned as a randomized controlled experimental study. A total of 112 women, 56 pregnant women in the experimental and control groups, will be included in the study. In this project, an automatic massage device will be used during the active phase (when the cervical opening is between 5-6 cm and 10 cm) and a massage device in line with the pregnancy-controlled sacral massage application protocol. Pregnant women are followed throughout the active phase of labor and indicators reflecting labor pain, progress of labor, and the health status of the mother and the baby are used with the "Individual Identification Form", "Visual Comparison Scale", "Labor Monitoring Form", "Mother's Birth Perception Scale (ADAS)". The satisfaction of midwives will be evaluated with the "Evaluation of Satisfaction Status of Midwives Form".
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Participating in the study voluntarily
having a cervical dilatation of 5-6 cm,
being between 38-40 weeks of pregnancy,- being a single fetus, having a cephalic presentation,
having a fetal weight between 2.5-4 kg,
Disqualifiers
having pregnancy complications
Those who have acute inflammatory problems in soft tissues, skin or joints, burns, nerve injuries, open wounds, rheumatoid and gouty arthritis,
those who have used any non-pharmacological methods will not be admitted.
Trial design
Parallel
Treatments tested in this trial
massage
Other interventionsacral massage
Treatment groups
Trial outcomes
Primary outcomes
stress
questionnaire, stress scale
Secondary outcomes
labor pain
pain scale, VAS
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: