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Recruiting NCT06992895

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

No phase Interventional Burn Wounds Burn

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: The visual presentation utilizes a three-dimensional holographic fan device..
Who it may be relevant to
Registry conditions: Burn Wounds, Burn. Basic parameters: 3 years — 12 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effect of Hologram Application on Pain, Anxiety and Fear Levels During Burn Dressing in Children: A Randomized Controlled Trial

Overview

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.

Detailed description

Burns are defined as traumas caused by damage to the skin and subcutaneous tissues caused by heat, chemicals, electricity, or radiation. The severity of these injuries can range from superficial dermal damage to deep tissue loss. Burns inflict physical harm and can also cause significant psychological distress, including anxiety and fear, particularly in children. The administration of dressing procedures during the post-burn treatment process is a particularly challenging aspect for pediatric patients, often accompanied by significant anxiety and discomfort. Consequently, interventions that target both physical and psychological relaxation are necessary during the treatment process.

Among the technologies developed for the purpose of distraction in recent years, hologram fans are particularly noteworthy. The creation of three-dimensional visualizations by hologram fans utilizes LED lights strategically positioned on high-speed rotating propeller blades, resulting in the presentation of realistic images to the viewer, seemingly suspended in the air. This visual illusion has the potential to mitigate the discomfort and anxiety associated with medical procedures, particularly by capturing the attention of children. Research has demonstrated that the presence of hologram enthusiasts during pediatric medical procedures, such as blood draws, has been shown to reduce levels of fear and stress in children. However, the efficacy of these materials in applications requiring extended use and high levels of discomfort, such as burn dressings, remains to be adequately examined through scientific research.

This randomized controlled experimental study will examine the effect of a hologram fan application on pain, anxiety, and fear levels in pediatric burn patients receiving dressing changes. The study will be conducted with children between the ages of 3 and 12 who are receiving burn treatment in the hospital and require dressings. Those who meet the sampling criteria will be randomly assigned to the experimental or control group. The experimental group will receive a hologram fan display during dressing, while the control group will not receive any distracting method. Children in both groups will have their pain, anxiety, and fear levels measured before, during, and after dressing. Additionally, their basic vital signs, such as pulse and respiration, will be recorded during each dressing application.

Interventions

  • 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

Primary outcome measures

  • The Wong-Baker Faces Pain Rating Scale: [Time frame: up to 1 hours]
Secondary outcome measures (1)
  • Children's Fear Scale (CFS): [Time frame: up to 1 hours]

Eligibility criteria

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%.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

Turkey (Türkiye) · 2 centers
  • Erzurum Provincial Health Directorate Erzurum City Hospital — Erzurum
  • Erzurum Provincial Health Directorate Erzurum City Hospital — Erzurum

Identifiers

NCT: NCT06992895 · AU-HF-MM-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗