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Virtual reality offers Drug-Free relief for morning sickness and sleep

NCT ID NCT07503080

Symptom relief Sponsor: Filiz Keskin Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only This study
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether using a virtual reality (VR) relaxation program can reduce nausea and vomiting, improve sleep quality, and increase comfort in pregnant women. About 90 women in early pregnancy (6-14 weeks) will either use VR relaxation or receive standard care. The goal is to find a safe, non-drug way to manage common pregnancy symptoms.

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

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

About 90 people

The number the study aims to enrol. It can still change while the study runs.

Started

Mar 2026

Expected to finish

Jan 2027

An estimate. End dates often move.

Lead sponsor

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

18 to 49 years

Sex

Female participants only

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Women between 6 and 14 weeks of gestation * Pregnancy-specific nausea and vomiting severity measured by PUQE-24 scale scoring 6-10 points * No obstetric complications in the current pregnancy * Aged 18-49 years * Not using antiemetic medications * Not using any pharmacological or non-pharmacological (alternative/complementary) interventions aimed at reducing nausea and vomiting * Willing and able to provide informed consent for participation in the study * Adequate Turkish language proficiency to read and understand study materials Exclusion Criteria: * Diagnosis of hyperemesis gravidarum (HG). * Presence of a diagnosed psychiatric disorder (e.g., depression, anxiety disorder). * Presence of neurological, vestibular, or visual conditions that may prevent the use of a virtual reality headset (e.g., vertigo, epilepsy, migraine, visual impairments). * Classified as a high-risk pregnancy (e.g., multiple pregnancy, history of diabetes, preeclampsia). * Presence of cognitive or communication impairments that would hinder active participation in the study.

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Conditions

The condition(s) this trial relates to.

insomnia Nausea

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Comfort Nausea and vomiting in pregnancy (NVP) Pregnancy Sleep quality

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Istanbul Esenler Nenehatun Family Health Center

    Istanbul, Esenler, 34220, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.