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The Effect Of The Labour Hopscotch On The Birth Process And Satisfaction (Labor Hopscotc)

A

Aydin Adnan Menderes University

Status

Completed

Conditions

Labor Duration
Labor Bain
and Birth Satisfaction During Physiologic Vaginal Birth

Treatments

Behavioral: Labor Hopscotch Exercise Program Group
Other: Standard Intrapartum Care

Study type

Interventional

Funder types

Other

Identifiers

NCT07330557
2023/46

Details and patient eligibility

About

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.

Full 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.

Enrollment

110 patients

Sex

Female

Ages

18 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

110 participants in 2 patient groups

Labor Hopscotch Program Group
Experimental group
Description:
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.
Treatment:
Other: Standard Intrapartum Care
Behavioral: Labor Hopscotch Exercise Program Group
Standard Intrapartum Care Group → Control
Other group
Description:
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.
Treatment:
Other: Standard Intrapartum Care
Behavioral: Labor Hopscotch Exercise Program Group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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