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The Effect of Virtual Reality and Music in High-Risk Pregnants on Non-Stress Test

NCT05495789 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 102

Last updated 2023-05-12

No results posted yet for this study

Summary

Aim: The aim of this study is to determine the effects of virtual reality and listening to music during the NST procedure on NST parameters, anxiety and satisfaction in high-risk pregnant.

Hypotheses H01 In the NST process, there is no difference between the NST parameters of the virtual reality group and the NST parameters of the control group.

H02 In the NST procedure, there was no difference between the anxiety score of the virtual reality group and the anxiety score of the control group.

H03 There is no difference between the satisfaction score of the group in which virtual reality was applied in the NST procedure and the satisfaction score of the control group.

H04 In the NST process, there is no difference between the NST parameters of the group to which the virtual reality is applied and the NST parameters of the musical group.

H05 In the NST procedure, there was no difference between the anxiety score of the group in which virtual reality was applied and the anxiety score of the music group.

H06 In the NST process, there is no difference between the satisfaction score of the group to which the virtual reality was applied and the satisfaction score of the music group.

H07 In NST operation, there is no difference between the NST parameters of the music group and the NST parameters of the control group.

H08 In the NST procedure, there was no difference between the anxiety score of the music group and the anxiety score of the control group.

H09 There is no difference between the satisfaction score of the music group and the satisfaction score of the control group in the NST procedure.

Conditions

  • High Risk Pregnancy

Interventions

OTHER

Virtual Reality

A relaxing video will be watched with virtual reality glasses.

OTHER

Music

Relaxing music will be played by wearing headphones.

Sponsors & Collaborators

  • NESLİHAN YILMAZ SEZER

    lead OTHER

Principal Investigators

  • AYKAN YÜCEL, Prof.Dr. · Ankara City Hospital Bilkent

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-01-09
Primary Completion
2023-02-10
Completion
2023-02-10

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05495789 on ClinicalTrials.gov