NCT07330557

Brief Summary

This study is designed to evaluate the effect of the Labor Hopscotch exercise on the birth process and maternal satisfaction. The study will be conducted as a randomized controlled trial at a tertiary-level maternity unit. Eligible pregnant women will be recruited during the active phase of labor and randomly assigned to either the intervention group or the control group. Participants in the intervention group will receive the Labor Hopscotch exercise program during labor in addition to standard intrapartum care. The control group will receive standard intrapartum care only. The Labor Hopscotch exercise program consists of structured physical movements adapted to the stages of labor and is implemented under the supervision of trained healthcare professionals. Data will be collected using standardized data collection forms, obstetric records, and validated measurement tools. Information related to sociodemographic characteristics, obstetric history, labor characteristics, and maternal experiences during labor will be recorded. The study is conducted in accordance with ethical principles and relevant institutional guidelines.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
110

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2024

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 30, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 30, 2025

Completed
8 days until next milestone

First Submitted

Initial submission to the registry

December 8, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

January 9, 2026

Completed
Last Updated

January 9, 2026

Status Verified

December 1, 2025

Enrollment Period

1.9 years

First QC Date

December 8, 2025

Last Update Submit

December 29, 2025

Conditions

Keywords

Labor hopscotchphysiologic vaginal birthlabor painlabor duration,birth satisfactionnon-pharmacological intrapartum care

Outcome Measures

Primary Outcomes (1)

  • Maternal Satisfaction Score Measured by a Validated Satisfaction Scale

    Maternal satisfaction will be assessed using a validated satisfaction scale. Total scores will be calculated according to the scale guidelines, with higher scores indicating greater maternal satisfaction.

    Within 24 hours postpartum

Study Arms (2)

Labor Hopscotch Program Group

EXPERIMENTAL

Participants undergo the Labor Hopscotch Exercise Program during the first stage of labor. This program is a non-pharmacological, behavioral intervention that encourages active movement. The exercises aim to shorten labor duration, reduce pain, and increase birth satisfaction. The program is performed under the supervision of trained healthcare professionals and provides ongoing intrapartum support.

Behavioral: Labor Hopscotch Exercise Program GroupOther: Standard Intrapartum Care

Standard Intrapartum Care Group → Control

OTHER

Participants received standard intrapartum care. This intervention included routine birth practices and care procedures. This group, which did not include any special exercises or additional interventions, served as the control group.

Behavioral: Labor Hopscotch Exercise Program GroupOther: Standard Intrapartum Care

Interventions

The institution's routine standard maternity care protocol Nonpharmacological or pharmacological comfort measures per standard care Includes routine clinical practices of healthcare professionals Hopscotch program is not implemented

Labor Hopscotch Program GroupStandard Intrapartum Care Group → Control

Throughout labor, active positions, movements, breathing exercises, and recordings are utilized, along with the hopscotch steps. Guided by a trained midwife/healthcare professional. Applied throughout the latent and active phases. Purpose: To reduce pain, facilitate labor progression, and minimize interventions.

Labor Hopscotch Program GroupStandard Intrapartum Care Group → Control

Eligibility Criteria

Age18 Years - 35 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility Details• Primiparous pregnant women
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Primiparous pregnant women with cervical dilation between 3cm and 5cm, expected to have a vaginal delivery and admitted to the delivery room,
  • Pregnant women aged 18-35,
  • Pregnant women with gestational age between 37-42 weeks,
  • Able to speak and understand Turkish, and
  • At least primary school graduates (as the scales will be completed using the self-report method) will be included.
  • Pregnant women without a history of mental or physical health problems,
  • Pregnant women without a history of high-risk pregnancy.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Aydın Kadın ve Çocuk Hastalıkları Hastanesi

Aydin, Turkey (Türkiye)

Location

Related Publications (1)

  • Carroll L, Thompson S, Coughlan B, McCreery T, Murphy A, Doherty J, Sheehy L, Cronin M, Brosnan M, O'Brien D. 'Labour Hopscotch': Women's evaluation of using the steps during labor. Eur J Midwifery. 2022 Sep 9;6:59. doi: 10.18332/ejm/152492. eCollection 2022.

MeSH Terms

Conditions

Labor Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Masking Details
No parties are masked in this study.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: A parallel design was chosen to compare the effects of the labor hopscotch program with standard intrapartum care. Participants are randomly assigned to either the intervention or control group, and outcomes are measured concurrently in both groups.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
doctoral student

Study Record Dates

First Submitted

December 8, 2025

First Posted

January 9, 2026

Study Start

January 1, 2024

Primary Completion

November 30, 2025

Study Completion

November 30, 2025

Last Updated

January 9, 2026

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will share

De-identified individual participant data will be made available to qualified researchers upon reasonable request after publication of the main study results. Data will be shared through a secure data repository, following ethical and privacy regulations.

Locations