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CompletedNCT07863687Updated Oct 7, 2026

Effect of Dance on Labor Pain in Primiparous Women

An interventional study of Labor dance in Labor Pain, sponsored by Medipol University. Completed at 7 sites in Turkey (Türkiye). Open to female participants aged 18 Years to 35 Years. Per ClinicalTrials.gov, last updated 2026-10-07.

Sponsored by Medipol University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 6 years 8 months after the study started (first participant enrolled Jan 2020, registered Oct 2026).
Updated Oct 7, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
Female
01

Study summary

This randomized controlled trial evaluated the effect of labor dance on labor pain in primiparous women. Primiparous women admitted for vaginal birth to seven hospitals of a university affiliated private hospital group in Istanbul, Turkiye, were randomly assigned to a labor dance group or a routine care group. Women in the dance group danced to music of their choice at 30 minute intervals from 4 cm cervical dilatation until full dilatation, using movements intended to widen the pelvic diameters, in addition to routine intrapartum care. Labor pain was measured with a Visual Analogue Scale at 4 cm dilatation and repeatedly until full dilatation. Cervical dilatation and the duration of the active phase of labor were recorded.

Read the detailed description

The study was approved by the Istanbul Medipol University Non-Interventional Clinical Research Ethics Committee on 13 November 2019 (decision no. 966). Because recruitment at the single initial center was slow during the coronavirus disease 2019 pandemic, an amendment approved on 20 July 2020 extended the study to six additional hospitals of the same group. Allocation followed a computer generated simple randomization list (random.org).

02

Conditions studied

  • Labor Pain

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Keywords

  • dance
  • primiparity
  • nonpharmacological pain management
  • midwifery
  • music
03

In context

Labor Pain

409 studies on the registry are indexed under Labor Pain; 69 are open to participants now.

This study's enrollment of 60 is below the median of 100 across 336 interventional studies indexed under Labor Pain.

Browse Labor Pain studies →

Lead sponsor

Medipol University is the lead sponsor of 320 studies on the registry; 87 are open to participants now.

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

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Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Primiparous women admitted for vaginal birth
  • 34 to 40 weeks of gestation
  • Singleton pregnancy with the fetus in vertex presentation
  • No known maternal or fetal anomaly or risk condition
  • No prior knowledge of labor dance
  • Willing to participate

Exclusion criteria

Exclusion Criteria:

  • Withdrawal from the study
  • Maternal or fetal complication related to the dance
  • Indication for cesarean birth
  • Need for labor induction
  • Need for pharmacological analgesia
05

Study design

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

Study arms

  • Experimental
    Labor dance

    Women were taught the dance movements after admission. From 4 cm cervical dilatation until full dilatation, they danced to self selected music every 30 minutes, repeating each chosen movement for one minute, in addition to routine intrapartum care.

    Behavioral: Labor dance

  • No intervention
    Routine care

    Routine intrapartum care of the hospital only. Pain and cervical dilatation were assessed at the same time points as in the intervention group.

Interventions

  • BehavioralLabor dance

    Warm up and stretching movements followed by movements intended to widen the pelvic diameters: pelvic tilt, small squat, squat, wide leg squat, clockwise and counterclockwise hip circles, sliding, and right and left leg forward hip rotation, performed to music chosen by the woman. Sessions were repeated every 30 minutes from 4 cm cervical dilatation until full dilatation, and each chosen movement was repeated for one minute.

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What researchers measure

Primary outcomes

  1. Labor pain intensity

    Pain intensity measured with a Visual Analogue Scale from 0 (no pain) to 10 (unbearable pain). Higher scores indicate more severe pain.

    Time frame: At 4 cm cervical dilatation (baseline) and at the end of each hour until full cervical dilatation, up to 4 hours

Secondary outcomes

  1. Time to full cervical dilatation

    Time from 4 cm to 10 cm cervical dilatation, in hours, assessed by hourly vaginal examination.

    Time frame: Assessed at the end of each hour from 4 cm cervical dilatation until full cervical dilatation, up to 4 hours

  2. Duration of the active phase of labor

    Duration of the active phase of labor, in minutes.

    Time frame: From 4 cm cervical dilatation until birth

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Study locations

7 sites
  • Bagcilar Medipol Mega University Hospital
    Istanbul, Turkey (Türkiye)
  • Camlica Medipol University Hospital
    Istanbul, Turkey (Türkiye)
  • Esenler Medipol University Hospital
    Istanbul, Turkey (Türkiye)
  • Kosuyolu Istanbul Medipol Hospital
    Istanbul, Turkey (Türkiye)
  • Ozel Nisa Hastanesi
    Istanbul, Turkey (Türkiye)
  • Pendik Medipol University Hospital
    Istanbul, Turkey (Türkiye)
  • Sefakoy Medipol University Hospital
    Istanbul, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: Yes — Deidentified individual participant data underlying the published results will be available from the corresponding author on reasonable request.

Time frame: Beginning with publication of the main results and for five years thereafter.

Access criteria: Researchers who submit a methodologically sound proposal to the corresponding author. Data will be shared under a data use agreement.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 7, 2026
Show all 1 update
  1. Oct 7, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

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Registry details

Key details

Study ID
NCT07863687
Lead sponsor
Medipol University
Responsible party
Şerife Çınar (Lecturer, Medipol University) — Principal investigator
First posted
Oct 7, 2026
Start date
Jan 30, 2020
Primary completion
Feb 28, 2021
Completion
Feb 28, 2021
Last update
Oct 7, 2026

Study contacts

Şerife Çınar, PhD
principal investigator · Medipol University

Oversight

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

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

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