Başakşehir Çam and Sakura City Hospital
Istanbul, 34408, Turkey (Türkiye)
NCT Number: NCT07759479
Study Description
Childbirth is a physiological process often accompanied by severe pain and prolonged labor, which may negatively affect maternal well-being and increase the likelihood of obstetric interventions. Non-pharmacological approaches that support physiological labor are recommended as part of evidence-based intrapartum care. The Rebozo technique is a traditional midwifery intervention involving rhythmic pelvic mobilization using a woven cloth to promote maternal comfort, facilitate fetal descent and rotation, and improve labor progression.
This single-center, parallel-group randomized controlled trial aims to evaluate the effectiveness of the Rebozo technique on labor pain intensity and labor duration among primiparous women during the active phase of labor. Eligible participants will be randomly assigned in a 1:1 ratio to either the intervention group, receiving the Rebozo technique in addition to routine intrapartum care, or the control group, receiving routine intrapartum care alone.
The primary outcomes are labor pain intensity, assessed using the Visual Analog Scale (VAS), and labor duration, measured from the active phase of labor (6 cm cervical dilatation) until birth. The findings are expected to provide evidence regarding the effectiveness, feasibility, and clinical applicability of the Rebozo technique as a safe, low-cost, non-pharmacological intervention to support physiological childbirth and improve maternal intrapartum outcomes.
Looking for future studies?
Notify Me18 year–45 year
Female
Interventional
Not applicable
Istanbul, 34408, Turkey (Türkiye)
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The Rebozo technique is a standardized non-pharmacological intervention performed using a traditional woven cloth to provide rhythmic pelvic mobilization during the active phase of labor. The intervention was administered in three sessions of approximately five minutes each by a trained researcher in addition to routine intrapartum care.
Routine intrapartum care was provided according to the institutional clinical protocol and included maternal and fetal monitoring, assessment of labor progress, supportive midwifery care, and obstetric management when clinically indicated.
Time frame: Immediately before the intervention and immediately after its completion, approximately 15 minutes after the baseline assessment during active labor.
Labor pain intensity was assessed using the 10-cm Visual Analog Scale for Pain, ranging from 0 (no pain) to 10 (worst imaginable pain). Higher scores indicate greater pain intensity and therefore a worse outcome. Scores were recorded immediately before and immediately after completion of the Rebozo intervention. The control group was assessed at corresponding time points.
Time frame: From the first documentation of 6 cm cervical dilatation until birth, assessed up to 24 hours.
The duration of the active phase of labor was calculated in minutes from the first documented cervical dilatation of 6 cm until birth, based on standardized partograph records. Higher values indicate a longer duration of labor.
Istanbul University
Other
Effects of the Rebozo Technique Applied During the Active Phase of Labor on Labor Pain Intensity and Labor Duration in Primiparous Women: A Parallel-Group Randomized Controlled Trial
Acronym: Rebozo Techniq
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07267351
Childbirth, Labor Pain
Nicosia, Cyprus
View Trial DetailsNCT06621238
Anxiety, Anxiety Disorders
Mardin, Artuklu/Mardin, Turkey (Türkiye)
View Trial DetailsNCT04814537
Agnosia, Analgesia
Boston, Massachusetts, United States
View Trial DetailsNCT05155826
Delivery Problem, Dystocia
Saint-Etienne, France
View Trial Details