The Effect of Using Nature Sounds and Virtual Reality During the Non-Stress Test

NCT07512999 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2026-04-06

No results posted yet for this study

Summary

The aim of this study is to examine the effect of using nature sounds and virtual reality during the non-stress test on fetal well-being, maternal anxiety, comfort, and satisfaction. The study sample will consist of all pregnant women admitted to the Non-Stress Test (NST) unit. A total of 150 women will be included in the sample: 50 for the virtual reality group, 50 for the nature sounds group, and 50 for the control group.

Conditions

  • Pregnancy - Prenatal Testing

Interventions

BEHAVIORAL

Virtual Reality

Women treated with virtual reality will be presented with videos of natural scenes (forest and sea) accompanied by nature sounds and asked to watch. The headset will be fitted before the procedure begins, and women will be instructed on how to continue watching the video while wearing the headset during the procedure.

BEHAVIORAL

Nature sounds

Women in the nature sounds group will be given the opportunity to listen to relaxing nature sounds (sea, rain, wind, river, birds) using MP3 players and headphones according to their preferences throughout the non-stress test.

BEHAVIORAL

Control

Participants in the control group received standard care (verbal information about procedure and a short written information about the procedure) and no intervention will perform.

Sponsors & Collaborators

  • Amasya University

    lead OTHER

Principal Investigators

  • Elif Keten Edis, PhD · Amasya University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-07-01
Primary Completion
2027-03-01
Completion
2027-03-31

More Related Trials

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 NCT07512999 on ClinicalTrials.gov