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AI-Generated Video Distraction Via Virtual Reality for Fear and Pain During Pediatric Circumcision

AI-Generated Video Distraction Via Virtual Reality for Procedural Fear and Pain in Pediatric Circumcision: A Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07824427
Enrollment
80
Registered
2026-09-17
Start date
2025-10-17
Completion date
2026-08-11
Last updated
2026-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Artificial Intelligence (AI), Child, Circumcision, Male, Digital Health, Fear, Generative Artificial Intelligence, Procedural Pain Relief, Virtual Reality

Keywords

Circumcision, Male, Virtual Reality, Generative Artificial Intelligence, Child

Brief summary

This randomized controlled trial evaluated the effect of artificial intelligence-generated video distraction delivered via virtual reality on procedural fear and pain in children undergoing circumcision. A total of 80 children aged 4-12 years were assigned to an intervention group (n=40) or a control group (n=40). Children in the intervention group received AI-generated video distraction via virtual reality, whereas children in the control group received routine care. Pain and emotional responses were assessed from the perspectives of the child, parent, and nurse. Physiological parameters were also measured before and after the procedure. The study aimed to determine whether AI-generated video distraction delivered via virtual reality reduces procedural fear and pain during pediatric circumcision.

Interventions

BEHAVIORALAI-Generated Video Distraction via Virtual Reality

Artificial intelligence-generated video content is presented through a virtual reality headset as a distraction intervention for children undergoing circumcision. The intervention is intended to reduce procedural fear and pain.

Sponsors

Yuzuncu Yil University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
4 Years to 12 Years
Healthy volunteers
Yes

Inclusion criteria

* Male children aged 4 to 12 years. * Children scheduled to undergo circumcision. * Participation in the study with parental consent.

Exclusion criteria

\- Children who did not meet the study inclusion criteria.

Design outcomes

Primary

MeasureTime frameDescription
Pain Scores at the Post-Test AssessmentImmediately after the circumcision procedurePain intensity will be assessed using the Wong-Baker FACES Pain Rating Scale. The scale ranges from 0 to 10, where 0 indicates no pain and 10 indicates the worst pain. Higher scores indicate greater pain intensity and therefore a worse outcome. Pain will be rated independently by the child, parent, and nurse.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 18, 2026