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Clinical Trials in Turkey / NCT07752693
Recruiting Not applicable

The Effect Of Partner-Assısted Rebozo Technıque On Labor Paın And Satısfactıon In Prımary Pregnant Women

NCT07752693 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-05-01
Last updated
2026-08-11

Condition(s) studied

Labor Pains

Investigational drug(s) / intervention(s)

Rebozo Technique

Rebozo Technique: Rebozo technique is a traditional Mexican practice that involves relaxation, rhythmic rocking, pelvic mobilization, and position changes during pregnancy and childbirth. Theses and research examining the effects of this technique on labor indicate that the rebozo method can contribute to shortening labor time and allow the mother to be more active during delivery. In our study, unlike other rebozo techniques, the aim is to provide "partner support." The rebozo technique will be applied with partner support during the three active phases of cervical effacement and dilation (5cm, 6-8cm, and 9-10cm), and the results will be recorded.

Study summary

The main objective of this study is to examine the effect of the rebozo technique, applied with partner support, on labor pain and birth satisfaction in primiparous pregnant women. This research is planned as a randomized controlled experimental study. A total of 64 pregnant women, 32 in the control group and 32 in the experimental group, who meet the sample selection criteria and agree to participate in the study, will constitute the sample of the study. Participants included in the study will be administered the Informed Consent Form, the "Demographic Information Form" created by the researcher, the "Fathers' Participation in Birth Scale", VAS scoring, "Birth Care Guide", "Observation Form Regarding Labor" and the "Birth Satisfaction Scale". Data will be analyzed using appropriate statistical methods. It is expected that the results obtained will contribute to the use of non-pharmacological methods in the birthing process and the support of partner participation.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
49 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Those aged between 18 and 49, * Between 37-42 weeks of gestation, * Primiparous pregnancy, * In head presentation, the fetus is singular, * Those who have not been diagnosed with a high-risk pregnancy, * Someone who understands and can speak Turkish, * In the active phase (5cm and above), * The spouse is allowed to be present at the birth. Exclusion Criteria: * Those who experienced adjustment problems in the study, * Patients who require an emergency cesarean section, * Pregnancy with a known high-risk diagnosis (IUGR, fetal anomaly, polyhydramnios or oligohydramnios, presentation anomaly, multiple pregnancy, preeclampsia, etc.)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Çerkezköy State Hospital Tekirdağ Turkey (Türkiye) Recruiting

More Istanbul Saglik Bilimleri University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07752693 on ClinicalTrials.gov ↗ ← All trials in Turkey