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Virtual reality may help women feel less pain and fear during abortion

NCT ID NCT07288047

Symptom relief Sponsor: Study Investigator Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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) headset showing calming nature videos can reduce pain and anxiety during a first-trimester procedural abortion. Seventy-two adults will either receive usual care (pain medication and local anesthetic) or usual care plus the VR headset. Researchers will measure pain and anxiety scores before and after the procedure, and check satisfaction one week later.

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 headset (Meta Quest 3S) showing meditative nature videos
What this could lead to
If it works, this could offer a simple, drug-free way to ease pain and anxiety during a first-trimester abortion, improving patient comfort and satisfaction.
What could go wrong
This is a small, early-stage trial with only 72 people. The VR headset may not significantly reduce pain or anxiety compared to usual care alone. Some people may feel dizzy or uncomfortable using VR.

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 72 people

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

Started

May 2026

Expected to finish

Oct 2026

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 years and older

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: * Patients at Planned Parenthood of Western Pennsylvania who have decided to undergo and are eligible for a procedural abortion. * 18 years old or older * \<14 weeks gestation on day of abortion * Able to comprehend written English * Willing to comply with the study protocol * Willing and able to provide informed consent Exclusion Criteria: * History of vertigo * History of epilepsy * Claustrophobia * Significant hearing or visual impairments (such as deafness or blindness) * Require hearing aids * Have an implanted medical device, such as cardiac pacemaker or defibrillator * Require misoprostol for cervical preparation * Prior unsuccessful attempt at abortion during this pregnancy

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Conditions

The condition(s) this trial relates to.

agnosia Personal Satisfaction

As listed by the trial registrant

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

Abortion, first trimester Anxiety after surgery Pain after surgery Pain management Satisfaction Satisfaction with care

How to take part

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

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    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

  • Center for Family Planning Research, Magee-Womens Hospital

    RECRUITING

    Pittsburgh, Pennsylvania, 15213, United States

  • Planned Parenthood of Western Pennsylvania

    RECRUITING

    Pittsburgh, Pennsylvania, 15213, United States

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