The Effect of Pregnant-controlled Sacral Massage on Mothers' Labor Pain, Perception, Process and Midwives' Satisfaction

ConditionsLabor PainLabor
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorOsmaniye Korkut Ata University

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • massage

    Other intervention

    sacral massage

Treatment groups

112 Participants
are divided into 2 treatment groups
Group A: control groupNo intervention 0 interventions
Group B: experimental groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

stress

questionnaire, stress scale

Time frame
1 day

Secondary outcomes

1

labor pain

pain scale, VAS

Time frame
1 day

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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