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The Effect Of The Labour Hopscotch On The Birth Process And Satisfaction

NCT07330557 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 110

Last updated 2026-01-09

No results posted yet for this study

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.

Conditions

  • Labor Duration
  • Labor Bain
  • and Birth Satisfaction During Physiologic Vaginal Birth

Interventions

BEHAVIORAL

Labor Hopscotch Exercise Program Group

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.

OTHER

Standard Intrapartum Care

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

Sponsors & Collaborators

  • Aydin Adnan Menderes University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-01-01
Primary Completion
2025-11-30
Completion
2025-11-30

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07330557 on ClinicalTrials.gov