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The Effect of Virtual Reality Glasses on Labor Pain

NCT ID: NCT01687933

Last Updated: 2012-09-19

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

PHASE2/PHASE3

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-02-28

Study Completion Date

2012-08-31

Brief Summary

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There are different medicinal and non medicinal methods to control labor pain. Today, much attention has been on non medicinal methods because of limitations and complications of medical procedures. Virtual reality is a new and promising method of diversion of mind that may have an impact on labor pain. This study was conducted to determine the effect of virtual reality on the first stage of labor pain.

Detailed Description

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Conditions

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Labor Pain Anxiety

Keywords

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Labor pain Virtual reality the first stage of labor Pain relief Simulator

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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three-dimensional glasses (Virtual Reality glasses)

Women in case group used the glasses for 30 minutes

Group Type EXPERIMENTAL

three-dimensional glasses(manufactor Vuzix,wrap 920)

Intervention Type DEVICE

The samples were randomly allocated to use three-dimensional glasses for 30 minutes in order to reliving labor pain.

usual care

Women in control group did not use the glasses.

Group Type EXPERIMENTAL

usual care

Intervention Type OTHER

Women in Control group did not use the glasses.

Interventions

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three-dimensional glasses(manufactor Vuzix,wrap 920)

The samples were randomly allocated to use three-dimensional glasses for 30 minutes in order to reliving labor pain.

Intervention Type DEVICE

usual care

Women in Control group did not use the glasses.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Iranian
* low risk pregnancy
* primipara

Exclusion Criteria

* vision or ear disorders
* History of motion sickness or headaches
* psychological disease or Addiction
Minimum Eligible Age

18 Years

Maximum Eligible Age

29 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Mashhad University of Medical Sciences

OTHER

Sponsor Role lead

Responsible Party

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Samira Ebrahimzadeh Zagami

MUMS

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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Virtual Reality System

Identifier Type: -

Identifier Source: org_study_id