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Recruiting NCT07683715

NCT07683715 Virtual Reality-Assisted Cast Application in Children With Forearm Fractures

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Clinical Trial Summary
NCT ID NCT07683715
Status Recruiting
Phase
Sponsor Başakşehir Çam & Sakura City Hospital
Condition Forearm Fractures
Study Type INTERVENTIONAL
Enrollment 120 participants
Start Date 2025-12-05
Primary Completion 2026-08-30

Eligibility & Interventions

Sex All sexes
Min Age 4 Years
Max Age 15 Years
Study Type INTERVENTIONAL
Interventions
Virtual Reality-Based Educational AnimationStandard Care

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 120 participants in total. It began in 2025-12-05 with a primary completion date of 2026-08-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * 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. Exclusion Criteria: * 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.

Contact & Investigator

Central Contact

Lezgin Mert, MD

✉ lezginmert@gmail.com

📞 +905056003904

Frequently Asked Questions

Who can join the NCT07683715 clinical trial?

This trial is open to participants of all sexes, aged 4 Years or older, up to 15 Years, studying Forearm Fractures. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07683715 currently recruiting?

Yes, NCT07683715 is actively recruiting participants. Contact the research team at lezginmert@gmail.com for enrollment information.

Where is the NCT07683715 trial being conducted?

This trial is being conducted at Istanbul, Turkey (Türkiye).

Who is sponsoring the NCT07683715 clinical trial?

NCT07683715 is sponsored by Başakşehir Çam & Sakura City Hospital. The trial plans to enroll 120 participants.

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