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

Effect of the Labour Hopscotch Method on the Labor Process and Maternal Satisfaction: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07330557
Acronym
Labor Hopscotc
Enrollment
110
Registered
2026-01-09
Start date
2024-01-01
Completion date
2025-11-30
Last updated
2026-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Keywords

Labor hopscotch, physiologic vaginal birth, labor pain, labor duration,, birth satisfaction, non-pharmacological intrapartum care

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.

Detailed description

This study aims to evaluate the effect of the Labor Hopscotch exercise on the labor process and maternal experience. The study is designed as a randomized controlled trial including eligible pregnant women. Participants will be allocated to an intervention group or a control group, and predefined outcomes will be assessed using standardized procedures.

Interventions

BEHAVIORALLabor 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.

OTHERStandard 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

Aydin Adnan Menderes University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

No parties are masked in this study.

Intervention model description

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.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
Maternal Satisfaction Score Measured by a Validated Satisfaction ScaleWithin 24 hours postpartumMaternal 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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026