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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

112 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-07-22

Study Completion Date

2024-09-22

Brief Summary

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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".

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Detailed Description

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Conditions

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Labor Pain Labor

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants

Study Groups

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control group

Group Type NO_INTERVENTION

No interventions assigned to this group

experimental group

Group Type EXPERIMENTAL

massage

Intervention Type OTHER

sacral massage

Interventions

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massage

sacral massage

Intervention Type OTHER

Eligibility Criteria

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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

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.

Minimum Eligible Age

18 Days

Maximum Eligible Age

45 Days

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes