Positioned group
Behavioralapplied a side-lying position (20 minutes) on the occiput side and a prostrate position (15 minutes).
NCT Number: NCT06928038
This is a randomized controlled experimental study to determine the effect of maternal position on the progression of labour in deliveries in which the foetus is in the occiput posterior position.
The study included 148 gravidas admitted to a private Istanbul hospital, who consented to participate. They were divided into intervention and control groups (n=72). The intervention group assumed a side-lying position on the occiput side for 20 minutes, a prostrate position for 15 minutes, then leaned towards the bed's head for 10 minutes (rest), followed by another 20-minute side-lying position. The control group received routine delivery care.
Looking for future studies?
Notify Me18 year and older
Female
Interventional
Not applicable
This is a randomized controlled experimental study. The research was carried out in a private hospital in Istanbul. The population of the study covered gravidas who were admitted to the hospital for delivery with the foetus in the occiput posterior position in labour. The sample of the study included 148 volunteering gravidas, who were divided into intervention and control groups.
Research Hypotheses:
H1: In deliveries where the foetus is in the occiput posterior position, the positions given to the mother help the foetus to rotate to the occiput anterior position.
H2: Positions given to the mother in the occiput posterior position do not affect the Apgar score.
H3: In deliveries where the foetus is in the occiput posterior position, the positions given to the mother reduce the rate of interventional delivery.
Implementation :
After the occiput posterior position was established by ultrasonography, the gravidas included in the study were randomized into 2 groups as intervention and control groups. The intervention group was given the following positions during labour:
After 1 hour, the gravida was placed in a side lying position on the side of the occiput. Digital vaginal examination was repeated at 2 hour intervals. If the foetus has rotated to the occiput anterior position, the women was released (could walk, stand, allowed to do as she pleased). If the occiput posterior continued but the descent of the head was progressing, she was tilted to the side of the occiput on the delivery table after the dilatation is completed and instructed to push (keeping the upper leg up). At the time of coronation, she was laid on her back and delivered. If there was no head descent or rotation according to the digital vaginal examination finding, time was allowed for dilatation to reach 7-8 cm in the primiparae. Caeserean section (C/S) was scheduled if there was no change. If the posh was not open in multiparous patients and the head was at -3 -2, amniotomy was performed and time was allowed until dilatation was complete. However, C/S was planned if digital vaginal examination performed with an interval of 2 hours did not indicate progress.
The control group was followed up in the routine delivery room, and no positioning was done.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Inability to understand Turkish
applied a side-lying position (20 minutes) on the occiput side and a prostrate position (15 minutes).
Time frame: from labor to the end of the delivery
cesarean section, spontaneously deliver
Time frame: From labor to the expulsion stage
right - left occiput posterior; right - left occiput transverse; right - left occiput anterior
Time frame: duration of expulsion phase
The time from completion of dilatation to birth of the baby
Biruni University
Other
The Effect of Maternal Position on Labour Progression in Deliveries With the Foetus in the Occiput Posterior Position
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.
NCT06379048
Episiotomy Wound, Labor; Prolonged, Second Stage
Istanbul, Basaksehir, Turkey (Türkiye)
View Trial DetailsNCT06210087
Evidence-Based Practice, Fetal Acidosis Complicating Labor and Delivery
Elâzığ, Turkey (Türkiye)
View Trial DetailsNCT02963337
Labor Pain, Labor; Prolonged, First Stage
Ljubljana, Slovenia
View Trial DetailsNCT05155826
Delivery Problem, Dystocia
Saint-Etienne, France
View Trial Details