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

Not Applicable

Not yet recruiting

• Conditions: Labor; Labor Pain
• Interventions: Other: massage

• Registration Number: NCT06499402
• Lead Sponsor: Osmaniye Korkut Ata University

Brief Summary

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".

Detailed Description

Not available

Study Timeline

• Status Verified: 2024-07
• Study First Submitted: 2024-07-04
• Study First Submitted QC: 2024-07-10
• Last Update Submitted: 2024-07-11
• Study First Posted: 2024-07-12
• Last Update Posted: 2024-07-15
• Study Start: 2024-07-22
• Primary Completion: 2024-08-22
• Study Completion: 2024-09-22

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: Female
• Target Recruitment: 112

Inclusion Criteria

• 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,
• having no vision-hearing problems,
• having communication and cooperation skills

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Exclusion Criteria

• 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.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
experimental group	massage	-

Primary Outcome Measures

Name	Time	Method
stress	1 day	questionnaire, stress scale

Secondary Outcome Measures

Name	Time	Method
labor pain	1 day	pain scale, VAS