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Clinical Trials in Turkey / NCT06992895
Recruiting Not applicable

The Effect of Hologram Application on Pain, Anxiety, and Fear Levels in Children During Burn Dressing

NCT06992895 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-10-15
Last updated
2026-04-13

Condition(s) studied

Burn WoundsBurn

Investigational drug(s) / intervention(s)

The visual presentation utilizes a three-dimensional holographic fan device.

The visual presentation utilizes a three-dimensional holographic fan device.: This study is among the first to examine the effect of holographic fan technology on pain, anxiety, and fear in children during burn dressing. In comparison with other distraction methods, holographic fans represent a novel technological intervention designed to mitigate pain and anxiety by engaging children's attention through the use of visual illusions. Furthermore, extant studies on the effectiveness of this technology during prolonged and distressing procedures, such as burn dressing, have been found to lack sufficient data.

Study summary

The process of dressing burn injuries has been shown to cause both physical and psychological difficulties. In children, this process is particularly associated with intense pain and anxiety. Consequently, in addition to pharmacological interventions, non-pharmacological methods such as distraction are employed. In recent years, the utilization of holograms as a method of alleviating pain has emerged as a novel approach. The employment of these visual illusions has been demonstrated to effectively distract children, thereby providing a means of reducing discomfort. The objective of this thesis is to evaluate the effects of hologram application on pain, anxiety, fear, and vital signs during burn dressing in children.

Eligibility

Sex
ALL
Min age
3 Years
Max age
12 Years
Healthy volunteers
Accepted
Inclusion Criteria: * The subject has indicated their willingness to participate in the study. Physical and mental health. * The age range of the subjects included in this study was from 3 to 12 years of age. * The subject had never previously engaged in the practice of dressing a burn. * The presence of only second degree burns * Burn percentage is under 10% Exclusion Criteria: * The subject is unwilling or unable to provide informed consent or assent (if applicable). * The subject has a history of significant physical or mental health disorders that may interfere with participation in the study. * The subject is younger than 3 years old or older than 12 years old. * The subject has previously engaged in the practice of burn dressing or similar procedures. * The presence of burns other than second-degree burns (e.g., first-degree or third-degree burns). * The percentage of burn area is greater than 10%.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Erzurum Provincial Health Directorate Erzurum City Hospital Erzurum Yakutiye Recruiting
Erzurum Provincial Health Directorate Erzurum City Hospital Erzurum Yakutiye Not Yet Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06992895 on ClinicalTrials.gov ↗ ← All trials in Turkey