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Holograms may replace needles for burn dressing pain

NCT ID NCT07244653

Symptom relief Sponsor: Gamze BULUT Source: ClinicalTrials.gov ↗

What the study statuses mean

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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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jul 24, 2026 · Updated 3 times

Summary

This study tests whether showing 3D hologram videos during burn dressing changes can reduce pain, anxiety, and fear in patients. 70 adults will be randomly assigned to either watch a hologram or receive standard care. The hologram projects interactive images into the air without any headset, aiming to distract patients from the painful procedure.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
3D hologram video distraction
What this could lead to
If it works, this could offer a drug-free way to ease pain and anxiety during burn dressing changes, improving patient comfort and cooperation.
What could go wrong
This is a small, early-stage trial with only 70 participants, so results may not apply to everyone. The hologram effect may not be strong enough to meaningfully reduce pain or anxiety.

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

72 people

The number who actually took part.

Started

Dec 2025

Expected to finish

Sep 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 to 65 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 * Between the ages of 18-65, * Able to read, write, and speak Turkish, * Not participating in any other clinical research at the same time, * Patients without epilepsy who have been admitted to the burn unit for treatment, * Non-infected cases, * Patients who have not undergone minor and/or major surgical procedures (fasciotomy, escharotomy, amputation, etc.) that may affect the wound healing process, * Without any cognitive, affective, or other problems that may prevent them from communicating verbally and understanding information, * Total body surface area (TBSA) of burns is less than 20% of the second degree; Patients with a 3rd degree burn below 15% (20% in 2nd degree patients; sedation required in 3rd degree patients above 15%), * 2nd and 3rd degree burns in the granulation stage (2nd and 3rd degree burns requiring treatment and high pain levels), * Not affected by different non-drug treatment methods that would affect pain, * Undergoing standard analgesia protocol, * No burns on the head, ears, or face, * Burns of hot liquid contact (scald), * Patients whose initial burn dressing was performed at the burn center where the study was conducted, with dressing changes every two days and at least two consecutive dressing changes were included in the study. Exclusion Criteria * Patients who developed any complications during two consecutive dressing changes (sepsis, fever, hemodynamic instability, wound infection, new trauma to the burn area, or conditions requiring additional surgical intervention, etc.), * Patients diagnosed with epilepsy were excluded from the study due to the risk of seizure triggering by photosensitive stimuli.

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Conditions

The condition(s) this trial relates to.

anxiety anxiety disorder burn Pain

As listed by the trial registrant

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

Anxiety Burn pain Burn patients FEAR

Contacts and locations

Locations

  • Atatürk Universty, Nursing faculty

    Erzurum, Erzurum, 25000, Turkey (Türkiye)

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