Virtual Reality Effect on Labor Pain and Satisfaction

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

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-06-01

Study Completion Date

2021-11-08

Brief Summary

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The primiparous women wore virtual glasses during labor, playing games and exercising. pregnant women were divided into two groups. Experimental and control groups each consisted of 60 pregnant women.

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Detailed Description

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Aim: The research was carried out to determine the effect of virtual reality application in labor on perceived labor pain and satisfaction levels in primiparous.

Material and Method: The study was conducted in a randomized controlled manner with a total of 120 primiparous women who applied to the delivery room of Elazig Fethi Sekin City Hospital between June 2020 and June 2021 (60 Experiments, 60 Controls). The pregnant women in the experimental group were played by the researcher during the active and transitional phases of labor with virtual reality glasses, which were designed for research and included methods used to cope with labor pain. Except for routine care, no application was made to the pregnant women in the control group. In order to determine the pain level of the pregnant women, SDS and SCS were applied four times, before and after the Virtual Reality applications. After delivery, DME-C was applied to both groups.

Conditions

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Satisfaction Labor Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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experimental group

virtual reality application

Group Type EXPERIMENTAL

Virtual Reality Application

Intervention Type OTHER

The pregnant women in the experimental group were played by the researcher during the active and transitional phases of labor with virtual reality glasses, which were designed for research and included methods used to cope with labor pain

control group

standard care group

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Virtual Reality Application

The pregnant women in the experimental group were played by the researcher during the active and transitional phases of labor with virtual reality glasses, which were designed for research and included methods used to cope with labor pain

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* All pregnant women who were able to communicate verbally
* Between 37-42 weeks of pregnancy
* Single, live fetus and head presentation
* Cervical opening \<4 cm based on the labor follow-up form at admission to the delivery room, were included in the sample

Exclusion Criteria

* Women with a risky pregnancy diagnosis (such as preeclampsia, placenta previa, gestational diabetes)
* Obstetric complications in labor (such as fetal distress, bleeding)
* Visual and hearing problems
* Any pharmacological pain-reducing method applied, were excluded from the study

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes