Effect of Immersive Virtual Reality on Pain in Different Dental Procedures in Children (NCT06794788) | Clinical Trial Compass
CompletedNot Applicable
Effect of Immersive Virtual Reality on Pain in Different Dental Procedures in Children
Jordan154 participantsStarted 2019-07-01
Plain-language summary
the current study aims to assess virtual reality as an effective pain management technique for children undergoing different dental procedures.
The iWear is the immersive virtual reality device was used for this study from (Vuzix®, Rochester, New York, USA). The iWear consists of a lightweight high-end pair of video headphones that contain pair of VR goggles
Who can participate
Age range
5 Years – 12 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Children aged 5-12 years
* Good general health,
* Taking no medications,
* Willingness to participate in the study
Exclusion Criteria:
* Subjects with a convulsive disorder,
* Subjects with a history of serious vestibular abnormalities,
* Subjects with musculoskeletal disorders, or developmental delay taking psychotropic drugs
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
The Wong-Baker Faces
Timeframe: through study completion, an average of 2 years
2
Visual Analog Scale (VAS)
Timeframe: through study completion, an average of 2 years
3
The 'Face, Legs, Activity, Cry, Consolability' (FLACC) scale
Timeframe: through study completion, an average of 2 years