Maternal Position's Effect on Labor Progression in Occiput Posterior Deliveries

The Effect of Maternal Position on Labour Progression in Deliveries With the Foetus in the Occiput Posterior Position

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.

Study Overview

• Status: Completed
• Conditions: Delivery Problem; Labor; Prolonged, Second Stage
• Intervention / Treatment: Behavioral: Positioned group

Detailed Description

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:

1. The gravida is given a side-lying position on the side of the occiput for 20 minutes. She is laid with the lower leg bent and the upper leg extended.
2. Then the prostrate position is given for 15 minutes (This position is where the pregnant women kneels while lowering her forehead to touch the bed or floor).
3. After this position, they are allowed to rest for 10 minutes by leaning towards the head of the bed.
4. Then, they are given a side-lying position again on the side of the occiput for 20 minutes.

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.

• Study Type: Interventional
• Enrollment (Actual): 148
• Phase: Not Applicable

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• Gravidas aged 18 years or older
• Between 36 and 42 weeks of gestation
• Willing to participate in the study
• Expected to deliver vaginally
• Not classified as high-risk
• No obstetric or medical complications during labor
• Single, healthy fetus in one of the following positions: occiput posterior, left occiput posterior, right occiput posterior, left occiput transverse, or right occiput transverse (confirmed via ultrasonography)
• Cervical dilation of at least 2-3 cm
• Estimated fetal weight between 2500 g and 3999 g
• No major congenital anomalies

Exclusion criteria:

Inability to understand Turkish

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Supportive Care
• Allocation: Randomized
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Intervention group; The positioned 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.	Behavioral: Positioned group; applied a side-lying position (20 minutes) on the occiput side and a prostrate position (15 minutes).
No Intervention: Control group; The control group was followed up in the routine delivery room, and no positioning was done.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
birth type of the baby	cesarean section, spontaneously deliver	from labor to the end of the delivery
Head position	right - left occiput posterior; right - left occiput transverse; right - left occiput anterior	From labor to the expulsion stage

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
duration of expulsion phase	The time from completion of dilatation to birth of the baby	duration of expulsion phase

Collaborators and Investigators

• Sponsor: Biruni University

Study record dates

Study Major Dates

• Study Start (Actual): February 1, 2015
• Primary Completion (Actual): December 30, 2016
• Study Completion (Actual): April 30, 2017

Study Registration Dates

• First Submitted: March 28, 2025
• First Submitted That Met QC Criteria: April 7, 2025
• First Posted (Actual): April 15, 2025

Study Record Updates

• Last Update Posted (Actual): April 17, 2025
• Last Update Submitted That Met QC Criteria: April 15, 2025
• Last Verified: April 1, 2025

More Information

Terms related to this study

• Keywords: Foetal malposition; Occiput posterior stance; Delivery positions
• Additional Relevant MeSH Terms: Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Obstetric Labor Complications; Pregnancy Complications; Dystocia
• Other Study ID Numbers: 10840098-241

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No