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Clinical Trials/CTRI/2024/09/073632
CTRI/2024/09/073632
Completed
Not Applicable

Effect of upright position on the duration of active phase of first stage of labour and labour outcome among primigravida at term in a tertiary care hospital: A Randomised controlled trial.

Jawaharlal Institute of Postgraduate Medical Education and Research1 site in 1 country80 target enrollmentStarted: September 20, 2024Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
80
Locations
1
Primary Endpoint
To assess the effect of upright position on the duration of the active phase of the first stage of labour and labour outcome

Overview

Brief Summary

This study is a randomised control trial to assess the effectiveness of the upright position on the duration of the active phase of the first stage of labour. Primigravida women who met the inclusion criteria were enrolled in the labour room using the convenience sampling method and a sequentially numbered, opaque, sealed envelope. Informed consent was obtained, and the procedure was performed. The baseline data was collected from both groups by using a socio-demographic proforma. In the experimental group, after taking consent Primigravida in spontaneous labor was given upright position (standing, hip dangling, walking, squatting, siting on birthing ball, sitting on the mat ) as long as women is comfortable for every 30min in an hour remaining 15min FHR and uterine contraction was assessed and for remaining 15min she took rest by sitting on the chair. After every 4 hours, PV was monitored and when she dilated to 7-8cm, for the remaining time she was made to sit on the chair till full cervical dilatation. The control group was asked to lie down in the left lateral or supine position as per hospital routine. FHR and uterine contraction was monitored for 15min in every 30min  duration. Routine PV was done every 4thhourly to check the cervical dilatation. After the delivery mode of delivery, degree of perineal tear, occurrence of PPH, APGAR scoring at 1min and 5min, and need for NICU admission were assessed.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
None

Eligibility Criteria

Ages
19.00 Year(s) to 39.00 Year(s) (—)
Sex
Female

Inclusion Criteria

  • Primigravida mother in spontaneous labour, singleton fetus with vertex presentation and 4-5cm cervical dilation at term.

Exclusion Criteria

  • Primigravida with contracted pelvis, undergoing induction of labour or presenting with fetal deceleration.
  • Primigravida with GDM, sever pre-eclampsia, eclampsia and fetal macrosomia.

Outcomes

Primary Outcomes

To assess the effect of upright position on the duration of the active phase of the first stage of labour and labour outcome

Time Frame: Every 30 minutes in an hour till full cervical dilation upright position will be given

Secondary Outcomes

  • To compare the labour outcome (cervical dilatation, mode of delivery, degree of perineal tear, PPH, APGAR scoring, and admission to NICU) between the control and intervention group(4th hourly for cervical dilatation and other after delivery.)

Investigators

Sponsor Class
Research institution and hospital
Responsible Party
Principal Investigator
Principal Investigator

SHRITY BRAHAMAN

Jawaharlal Institute of Postgraduate Medical Education and Research

Study Sites (1)

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