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

O

Osmaniye Korkut Ata University

Status

Not yet enrolling

Conditions

Labor Pain
Labor

Treatments

Other: massage

Study type

Interventional

Funder types

Other

Identifiers

NCT06499402
12345678

Details and patient eligibility

About

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".

Enrollment

112 estimated patients

Sex

Female

Ages

18 to 45 days old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

112 participants in 2 patient groups

control group
No Intervention group
experimental group
Experimental group
Treatment:
Other: massage

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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