Using virtual reality to manage pain in the emergency department
Virtual Reality Therapy for Pain Management at the Emergency Department
This study is testing whether virtual reality can help reduce pain for patients in the emergency department by comparing two different types of VR experiences.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 124 (estimated) |
| Ages | 16 Years to 99 Years |
| Sex | All |
| Sponsor | Radboud University Medical Center Academic / other |
| Locations | 1 site (Nijmegen, Gelderland) |
| Trial ID | NCT06089642 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of virtual reality (VR) therapy as a non-pharmacological approach to manage acute pain in patients admitted to the emergency department. The primary objective is to assess the impact of VR on patient-reported pain outcomes, while secondary objectives include evaluating its effect on analgesic use and patient-reported outcomes. The study will compare two types of VR interventions: one focused on distraction and the other on focused attention. Participants will be randomly assigned to receive either type of VR therapy during their treatment.
Who should consider this trial
Good fit: Ideal candidates are patients aged 16 and older who report moderate to severe pain (NRS score ≥4) and are willing to participate.
Not a fit: Patients with chronic pain, severe cognitive impairments, or those currently using opioids may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce the need for opioid prescriptions in emergency settings, leading to safer pain management.
How similar studies have performed: Previous studies have shown promising results for VR therapy in pain management, indicating potential for success in this novel application.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient ≥16 years admitted to ED * NRS pain at rest score ≥4 * Pain not acceptable for patient * Patient is willing and able to comply with the study protoc Exclusion Criteria: * Patients initially treated by another physician than the emergency physician (EP). * EMV \< 14 * History of dementia, seizures * Severe hearing/visual impairment not corrected * Headwounds or damaged skin with which comfortable and hygienic use is not possible. * Presentation to the ED because of chronic pain (≥3 months) exacerbation * Chronic opioid use (≥3 months) * Psychiatric disorders interfering with patients' understanding of the study protocol and informed consent
Where this trial is running
Nijmegen, Gelderland
- Radboud university medical center — Nijmegen, Gelderland, Netherlands (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.