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Virtual reality eases burn dressing pain and improves sleep

NCT ID NCT07306442

Symptom relief Sponsor: Abadan University of Medical Sciences 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 (VR) during wound dressing changes can reduce pain and improve sleep in adults with moderate to severe burns. Sixty patients took part, and the researchers compared VR to standard care. The goal was to see if VR could make a painful procedure more comfortable and help patients sleep better afterward.

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

60 people

The number who actually took part.

Started

Jan 2025

Finished

Jun 2025

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 60 years

Sex

Anyone

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: * \- Adult patients aged 18 to 60 years. * Deep partial-thickness or full-thickness burns covering 25% to 60% of total body surface area (TBSA). * Hemodynamic stability (systolic BP ≥90 mmHg, HR 60-100 bpm, no vasopressor use). * Ability to understand and comprehend Persian language. * Scheduled for at least one standardized, non-sedated wound dressing change procedure. Exclusion Criteria: * \- Diagnosed psychiatric or neurological disorder (e.g., schizophrenia, epilepsy). * Severe visual impairment (best-corrected visual acuity \<20/200) or auditory impairment. * History of motion sickness or VR intolerance. * Contraindications to VR use (e.g., active vertigo, uncontrolled hypertension).

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Conditions

The condition(s) this trial relates to.

burn Pain Parasomnias sleep disorder

As listed by the trial registrant

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

Burns Pain Sleep disturbances

Contacts and locations

Locations

  • Taleghani Burn and Trauma Hospital

    Ahvāz, Khuzestan, Iran

More trials for these conditions

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