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Labor PainNCT07863687

Effect of Dance on Labor Pain in Primiparous Women

A study testing Labor dance in people with Labor Pain, run by Medipol University at 7 sites in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 35 years, women only
Conditions the study is for
Labor Pain
What is being tested?
Labor dance
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
7 sitesTurkey (Türkiye)
Study dates
30 Jan 2020to 28 Feb 2021
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 35 years
  • Women only
  • No healthy volunteers
  • Adult

Who may be able to join

  • 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

Who cannot join

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

Trial locations and contacts

7 sites in 1 country.

7 sites in 1 country

Turkey (Türkiye)7 sites
  • Bagcilar Medipol Mega University Hospital

    Istanbul

  • Camlica Medipol University Hospital

    Istanbul

  • Esenler Medipol University Hospital

    Istanbul

  • Kosuyolu Istanbul Medipol Hospital

    Istanbul

  • Ozel Nisa Hastanesi

    Istanbul

  • Pendik Medipol University Hospital

    Istanbul

  • Sefakoy Medipol University Hospital

    Istanbul

Other trials in Turkey (Türkiye)

About this study

Official title: Determination of the Effects of Dance on the Management of Labor Pain in Primiparous Women: A Randomized Controlled Trial

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).

Conditions
Labor Pain
Being tested
Labor dance
Keywords
dance, primiparity, nonpharmacological pain management, midwifery, music
Medical subject headings
Labor Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Labor danceBehavioural

    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.

Study groups in NCT07863687
Study groupRoleWhat they receive
Labor danceExperimentalWomen 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.
Receives: Behavioral: Labor dance
Routine careNo interventionRoutine intrapartum care of the hospital only. Pain and cervical dilatation were assessed at the same time points as in the intervention group.

What is being measured

The primary outcome is the main question the study is designed to answer.

  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.

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

Secondary outcomes (2)
  1. Time to full cervical dilatation

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

    Measured: 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.

    Measured: From 4 cm cervical dilatation until birth

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Oct 2026
  2. Study start30 Jan 2020
  3. Primary completion28 Feb 2021
  4. Study completion28 Feb 2021

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
60 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07863687
Sponsor's protocol ID
LaborDancePainPrimipara2019
Status last verified
Oct 2026
First submitted
2 Oct 2026
Last updated
7 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Deidentified individual participant data underlying the published results will be available from the corresponding author on reasonable request.

Questions about this trial

What is this clinical trial studying?

A study testing Labor dance in people with Labor Pain, run by Medipol University at 7 sites in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 7 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 7 sites in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Labor pain intensity (time frame: At 4 cm cervical dilatation (baseline) and at the end of each hour until full cervical dilatation, up to 4 hours). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Oct 2026.

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