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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorAmasya University

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Being 18 years of age or older

Being at 32 weeks of gestation or beyond

Having a healthy pregnancy

Having a singleton and viable pregnancy

Disqualifiers

Having any communication impairment (language, vision, hearing, speech, etc.)

Having a physical or cognitive condition that prevents the use of the virtual reality application and nature sound Having a diagnosis of a high-risk pregnancy Having a diagnosis of a significant chronic (cardiac, renal, neurological, etc.) or psychiatric disorder (psychosis, neurosis, substance dependence, etc.) Having a multiple pregnancy Having a fetus with an anomaly Experiencing fetal distress requiring emergency intervention Having uterine contractions

Trial design

Design model

Parallel

Treatments tested in this trial

  • Virtual Reality

    Behavioral

    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.

  • Nature sounds

    Behavioral

    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.

  • Control

    Behavioral

    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.

Treatment groups

150 Participants
are divided into 3 treatment groups
Group A: Virtual reality groupExperimental treatment 1 intervention
Group B: Nature sounds groupExperimental treatment 1 intervention
Group C: Control groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

State-Trait Anxiety Inventory (STAI) Scale

The inventory was developed by Spielberger, Gorsuch, and Lushene in 1970. An adaptation, validity, and reliability study of the State-Trait Anxiety Scale in Turkish was conducted by Oner and Le Compte in 1983. The scale consists of two subdimensions: the state anxiety has 20 items and is used to determine what is felt at a specific moment under certain conditions, and the trait anxiety has 20 items and is used to determine what has been felt in the last 7 days. High scores from each subscale indicate a high level of anxiety. The Cronbach's a for the STAI ranges from 0.83 to 0.87

Time frame
Before the non-stress test and after the procedure is completed (20 minutes after the start of the procedure)
2

Visual Analog Scale for Comfort (VAS-Comfort)

The Visual Analog Scale (VAS) will be used to determine the comfort levels of the participants. Developed by Price et al. in 1983 for the purpose of evaluating subjective pain, the VAS is an easy-to-apply measurement method whose validity and reliability are accepted in the international literature (Price et al., 1987; Akbay, 2026). Based on the individual's subjective evaluation, the VAS is used not only to determine the level of pain but also to evaluate subjective conditions such as fatigue and discomfort. The Visual Analog Scale (VAS) is a 10 cm long scale that can be arranged vertically or horizontally, with endpoints defined by different expressions. In this study, to evaluate the comfort levels of individuals, the leftmost end of the scale will be defined as "0 = Not comfortable at all" and the rightmost end as "10 = Very comfortable". To make the scale more understandable and applicable, vertical lines and numerical values will be used on the horizontal line.

Time frame
After the non-stress test is completed (20 minutes after the start of the procedure)
3

Visual Analog Scale for Satisfaction (VAS-Satisfaction)

The VAS satisfaction form will be used to determine the satisfaction levels of the participants. The Visual Analog Scale (VAS) is a reliable and easily applicable measurement method with endpoints defined by different expressions, and is 10 cm long. VAS is also used to evaluate subjective states such as satisfaction. In this study, to evaluate the satisfaction levels of individuals, the leftmost end of the scale will be defined as "0 = Not satisfied at all" and the rightmost end as "10 = Very satisfied". In order to make the scale more understandable and applicable, vertical lines and numerical values will be used on the horizontal line.

Time frame
After the non-stress test is completed (20 minutes after the start of the procedure)
4

Non Stress Test Evaluation Form

The NST Evaluation Form will be used to determine the emotional state of participants during the NST procedure and to evaluate the results of the non-stress test (NST). The form includes variables such as NST recording time, basal fetal heart rate (FHR), presence and number of accelerations and decelerations, and whether it is evaluated as reactive or non-reactive. The National Institute of Child Health and Human Development 2008 guidelines will be used to evaluate the NST results.

Time frame
After the non-stress test is completed (20 minutes after the start of the procedure)

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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