Virtual Reality-Assisted Cast Application in Children With Forearm Fractures

Recruiting now · Not applicable

Conditions studied: Forearm Fractures, Procedural Anxiety, Doctor-Related Fear

In brief

This prospective randomized controlled trial will evaluate whether virtual reality can reduce procedural distress in children undergoing cast application for forearm fractures. Children will be assigned to either a virtual reality group or a standard care group. In the virtual reality group, children will watch a 3-minute child-friendly animated educational video using a VR headset during cast application. The video explains the casting procedure, how to protect the cast, and what the child should do after the cast is applied. The study will compare pain, anxiety, heart rate response, caregiver anxiety, and procedure-related fear between the two groups. The casting team will assess the child during the procedure. One day after cast application, each child will undergo an approximately 30-minute evaluation by a child psychiatry clinician who is blinded to group allocation. This follow-up assessment will evaluate the child's current anxiety, anxiety related to the cast experience, fear of returning to the hospital or doctor, and fear-related behaviors after the procedure.

Key facts

Study ID

NCT07683715

Run by

Başakşehir Çam & Sakura City Hospital

People needed

120

Starts

2025-12-05

Expected to finish

2026-09-01

Last updated by the study team

2026-07-06

Who can join

Age: 4 and older, up to 15. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Children aged 4 to 15 years.
• Diagnosis of an isolated forearm fracture requiring cast application with traction (greenstick injuries plastic deformation if NOT over 20 degrees bayonet apposition ok if <10 years and growth remains)
• First cast application for the current fracture episode.
• Typically developing children without a known developmental delay or cognitive impairment that would prevent participation in the study assessments.
• Ability of the child to understand age-appropriate instructions and respond to pain, anxiety, and fear-related assessments with caregiver assistance when necessary.
• At least one upper extremity free of immobilization, allowing heart rate assessment during the procedure.
• Parent or legal guardian able to provide written informed consent.
• Child assent when appropriate according to age and local ethics committee requirements.
• Ability and willingness of the child and caregiver to attend an approximately 30-minute blinded child psychiatry assessment 1 day after cast application.

You may not qualify if…

• Open forearm fracture.
• Multiple trauma or an additional painful injury that may affect pain, anxiety, or fear assessment.
• Need for emergency surgery, procedural sedation, or general anesthesia during cast application.
• Previous participation in this study.
• Known developmental delay, cognitive impairment, autism spectrum disorder with inability to complete study assessments, or severe psychiatric disorder that may interfere with questionnaire-based evaluation.
• Known epilepsy, photosensitive seizure disorder, severe motion sickness, vestibular disorder, or any condition considered unsafe for VR headset use.
• Visual or hearing impairment preventing use of the VR intervention or completion of the assessments.
• Head, face, or scalp injury preventing safe or comfortable use of a VR headset.
• Nausea, dizziness, or severe discomfort before the procedure that would prevent VR use.
• Refusal of the child or caregiver to participate.
• Inability to complete the 1-day child psychiatry follow-up assessment.

Where it is running

• Basaksehir Cam ve Sakura City Hospital — Istanbul, Istanbul, Turkey (Türkiye) (enrolling)

Full record on ClinicalTrials.gov

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