Using augmented reality and vibration to improve comfort during throat procedures
Using Augmented Reality With Vibroacoustic Stimulation to Improve the Patient Experience During In-Office Otorhinolaryngology Procedures
This study is testing if using augmented reality and vibrations can make throat procedures more comfortable for patients by reducing their anxiety and pain.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 80 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Virginia Academic / other |
| Locations | 1 site (Charlottesville, Virginia) |
| Trial ID | NCT06227039 on ClinicalTrials.gov |
What this trial studies
This study investigates the use of augmented reality (AR) and vibroacoustic stimulation to enhance patient comfort during in-office laryngology procedures. By applying the Gate Control Theory of Pain, the study aims to reduce anxiety and pain perception in patients undergoing these procedures without general anesthesia. Participants will be monitored for physiological indicators of stress, such as heart rate variability, alongside their self-reported experiences. The goal is to determine if these non-pharmacologic interventions can improve the overall patient experience and reduce the need for conversion to operating room procedures.
Who should consider this trial
Good fit: Ideal candidates are patients scheduled for office-based laryngology procedures at the University of Virginia.
Not a fit: Patients who are not undergoing laryngology procedures or those who may not tolerate the interventions may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance patient comfort and tolerance during in-office laryngology procedures, potentially reducing the need for more invasive interventions.
How similar studies have performed: While the use of sensory distraction techniques has been explored in other medical settings, this specific combination of AR and vibroacoustic stimulation in otolaryngology is novel and has not been previously tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients undergoing office-based laryngology procedure performed at home institution. Exclusion Criteria: * None
Where this trial is running
Charlottesville, Virginia
- UVA Fontaine Research Park Building 415 — Charlottesville, Virginia, United States (Recruiting)
Study contacts
- Principal investigator: James J Daniero, MD — University of Virginia
- Study coordinator: James J Daniero, MD
- Email: jjd5h@uvahealth.org
- Phone: 4349242040
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.