Virtual reality headsets calm anxious Moms-to-Be during fetal monitoring
NCT ID NCT07669090
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether watching calming nature videos through virtual reality glasses or doing progressive muscle relaxation exercises could reduce anxiety in high-risk pregnant women during a non-stress test (NST). 126 women were randomly assigned to one of three groups: VR, relaxation, or standard care. Researchers measured anxiety levels and physical signs like heart rate before and after the 20-minute test.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Virtual reality glasses and progressive muscle relaxation exercise
- What this could lead to
- If effective, this could offer a simple, drug-free way to help high-risk pregnant women feel calmer during routine fetal monitoring.
- What could go wrong
- This is a small, single-center study with no long-term follow-up. The results may not apply to all pregnant women, and the effect might be small or not clinically meaningful.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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126 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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Aug 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria Participants who meet all of the following criteria will be eligible for inclusion: * Aged 18 years or older; * Able to read, write, and understand Turkish; * At ≥28 weeks of gestation; * Having a singleton pregnancy; * Having eaten, emptied the bladder, and refrained from smoking and alcohol consumption for at least 2 hours before the non-stress test (NST) procedure; * Diagnosed by a physician with a high-risk pregnancy, including but not limited to preeclampsia, gestational diabetes mellitus, gestational hypertension, chronic hypertension, type 1 or type 2 diabetes mellitus, decreased fetal movement, premature rupture of membranes, threatened preterm birth, intrauterine growth restriction (IUGR), small for gestational age (SGA), oligohydramnios, or polyhydramnios. Exclusion Criteria Participants meeting any of the following criteria will be excluded: * Having a physical or mental condition that may impair communication; * Having a medical condition that may prevent participation in the intervention (e.g., musculoskeletal disorders, asthma); * Receiving magnesium sulfate (MgSO₄) treatment or having received MgSO₄ within the previous 2 hours. Withdrawal Criteria Participants will be withdrawn from the study if they: * Request to withdraw or no longer wish to continue participation in the study; * Are assigned to an intervention group and fail to participate in at least 80% of the intervention sessions.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Kanuni Sultan Suleyman Training and Research Hospital
Istanbul, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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