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Can virtual reality or a stress ball ease pain during childbirth stitches?

NCT ID NCT07499011

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested whether using virtual reality goggles or squeezing a stress ball can help reduce pain during episiotomy repair (stitches after childbirth). 112 women were randomly assigned to use VR, a stress ball, both, or standard care. The goal was to see which method works best for pain relief without medication.

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 goggles and stress ball
What this could lead to
If successful, this could provide a simple, drug-free way to ease pain during a common childbirth procedure.
What could go wrong
This is a small, completed study with 112 participants, so results may not apply to all women. Pain is subjective and distraction techniques may not work for everyone.

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

112 people

The number who actually took part.

Started

Dec 2025

Finished

Feb 2026

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 42 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 1. Women aged 18 to 42 years 2. Able to communicate and understand the study procedures 3. No vision, hearing, or perception problems 4. No physical problems preventing squeezing a stress ball 5. No diabetes mellitus 6. Undergoing episiotomy repair after vaginal birth 7. Willing to participate and provide informed consent Exclusion Criteria 1. Pre-existing chronic pain conditions 2. Severe perineal tear (3rd or 4th degree) 3. Development of any complication during the procedure 4. Women who did not consent to participate in the study 5. Women undergoing episiotomy repair with local anesthetic infiltration

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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

  • Feminine and Children Teaching Hospital and al _Rumaitha Hospital

    Samawah, Muthanna Governorate, Iraq

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