CClinicalTrials.gg
CompletedNCT07383181Updated Feb 3, 2026

Standing vs. Squatting Positions During Labor

An interventional study of Standing Position During Labor and Squatting Position During Labor in Labor Position and Maternal Birth Experience, sponsored by Biruni University. Completed at 1 site in Turkey (Türkiye). Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-03.

Sponsored by Biruni University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 7 months after the study started (first participant enrolled Jun 2025, registered Jan 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
82
Allocation
Randomized
Ages
18 Years and older
Sex
Female
01

Study summary

Background: Maternal position during labor is a key non-pharmacological strategy that supports physiological birth and women's active participation in the childbirth process. Although upright positions have been associated with favorable labor outcomes compared with supine positions, evidence directly comparing different upright positions-particularly in relation to maternal birth experience and perceived traumatic birth-remains limited.

Objective: This study aimed to compare the effects of standing and squatting positions during the first stage of labor on the birth process, birth comfort, pain intensity, and perceived traumatic birth experience among multiparous women.

Methods: This study was conducted using a comparative interventional design. A total of 82 multiparous women were included and allocated to either the standing group (n=41) or the squatting group (n=41) during labor. Data were collected using a personal information form, the Visual Analog Scale (VAS) for pain, the Labor Comfort Scale, and the Traumatic Birth Perception Scale. Outcomes were assessed during labor and within the first two hours postpartum. Statistical analyses included comparative and correlation analyses.

02

Conditions studied

  • Labor Position and Maternal Birth Experience
03

In context

Lead sponsor

Biruni University is the lead sponsor of 172 studies on the registry; 43 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Multiparous women aged ≥18 years
  • Gestational age between 38 and 42 weeks
  • Singleton pregnancy with cephalic presentation
  • Cervical dilatation ≥4 cm at admission
  • Low-risk pregnancy
  • Willingness to participate and provide written informed consent

Exclusion criteria

Exclusion Criteria:

  • Multiple pregnancy
  • Presentation anomalies
  • High-risk pregnancy (e.g., preeclampsia, gestational diabetes, placenta-related complications)
  • Fetal distress or known fetal anomalies
  • Any medical or obstetric condition requiring restricted mobility during labor
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
82 participants (actual)

Study arms

  • Experimental
    Standing Position Group

    Participants assigned to this group followed a standing position-based labor management approach during the first stage of labor.

    Behavioral: Standing Position During Labor

  • Experimental
    Squatting Position Group

    Participants assigned to this group followed a squatting position-based labor management approach during the first stage of labor.

    Behavioral: Squatting Position During Labor

Interventions

  • BehavioralStanding Position During Labor

    Women were encouraged to remain standing or to walk during contraction-related pain episodes throughout the first stage of labor under midwife supervision.

  • BehavioralSquatting Position During Labor

    Women were encouraged to assume the squatting position during contractions during the first stage of labor, supported by a birthing ball or bed rails according to preference.

06

What researchers measure

Primary outcomes

  1. Total Labor Duration

    Total duration of labor measured in hours.

    Time frame: From active labor onset (cervical dilatation ≥4 cm) to delivery

  2. Birth Duration

    Duration of the birth process measured in minutes.

    Time frame: From the active phase of labor to birth

07

Study locations

1 site
  • Nilgün Avcı
    Istanbul, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 3, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07383181
Lead sponsor
Biruni University
Responsible party
Nilgun Avci (Biruni University, Biruni University) — Principal investigator
First posted
Feb 3, 2026
Start date
Jun 1, 2025
Primary completion
Oct 30, 2025
Completion
Oct 30, 2025
Last update
Feb 3, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion