An Evaluation of Virtual Reality in Labor Pain During Vaginal Childbirth

NCT ID: NCT06677463

Last Updated: 2024-11-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-10-20

Study Completion Date

2024-10-30

Brief Summary

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This study will be conducted to evaluate the effect of applying virtual reality among laboring women during first stage of labor

Detailed Description

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This study will be conducted to evaluate the effect of applying virtual reality among laboring women during first stage of labor

Conditions

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An Evaluation of Virtual Reality in Labor Pain During Vaginal Childbirth

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

This study will be conducted to evaluate the effect of applying virtual reality among laboring women during first stage of labor
Primary Study Purpose

OTHER

Blinding Strategy

NONE

This study will be conducted to evaluate the effect of applying virtual reality among laboring women during first stage of labor

Study Groups

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An experimental study on the effect of virtual reality glasses on women during childbirth

An experimental study on the effect of virtual reality glasses on women during childbirth

Group Type EXPERIMENTAL

Virtual Reality

Intervention Type DEVICE

Studying the effect of virtual reality glasses on women during pregnancy, for the first time, it is also used to facilitate the birth process

Interventions

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Virtual Reality

Studying the effect of virtual reality glasses on women during pregnancy, for the first time, it is also used to facilitate the birth process

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Age between 20-25 years old .
* body mass index (BMI) 25- 32 kg/m2 .
* Primiparous .
* Highly educated.

Exclusion Criteria

* Laboring women with high risk pregnancy.
* Laboring women are taking pharmacological methods to relieve pain during first stage of labor.
* Low educated women
Minimum Eligible Age

20 Years

Maximum Eligible Age

25 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Kafrelsheikh University

OTHER

Sponsor Role lead

Responsible Party

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Amgad Hamed Abo motaa

physical therapy specialist for women health

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Fayiz Elshamy Elshamy Fayiz Elshamy, Professor of physical therapy

Role: PRINCIPAL_INVESTIGATOR

Fayiz Elshamy

Locations

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Menshawy general hospital

Tanta, Gharabia, Egypt

Site Status

Countries

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Egypt

Other Identifiers

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KFS IRB200-91

Identifier Type: -

Identifier Source: org_study_id

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