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NCT Number: NCT07599826

Active vs. Passive VR During Office-based ENT Procedures

The purpose of this research is to evaluate whether active virtual reality reduces pain and anxiety more effectively than passive virtual reality during office-based ENT procedures. The main procedures include exposure to virtual reality (passive calming scenery or interactive puzzle game) via Paperplane Therapeutics software with VR headset or glasses during common in-office ENT procedures, participant self-report surveys (GAD-7, PHQ-9, PEG, VAS, SUDS, Likert, experience questions), and physician post-procedure survey. The study will enroll individuals 18 years or older who are scheduled to undergo common office-based ENT procedures (turbinate reduction, nasal debridement, balloon sinuplasty, radiofrequency ablation, nasal polypectomy, eustachian tube dilation, vocal fold injection, or subglottic steroid injection) at Cedars Sinai.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Active and Passive VR:

  • Individuals 18 years old and older are included
  • Individuals undergoing the following common office-based ENT procedures: turbinate reduction, nasal debridement, balloon sinuplasty, radiofrequency ablation (Rhineaer/Vivaer), nasal polypectomy, eustachian tube dilation, vocal fold injection, or subglottic steroid injection
  • Able to consent
  • English speaking

Exclusion criteria

Active VR:

  • History of neurologic or seizure disorder, developmental delay, uncorrected visual impairment, motion sickness, vertigo, or inability to use a handheld controller
  • Any records flagged "break the glass" or "research opt out."

Exclusion criteria

Passive VR:

  • History of neurologic or seizure disorder, developmental delay, uncorrected visual impairment, motion sickness, or vertigo
  • Any records flagged "break the glass" or "research opt out."

Treatment and study plan

Virtual reality headset or goggles

Device

Exposure to virtual reality via Paperplane Therapeutics software with VR headset or glasses during common in-office ENT procedures

Primary outcomes

  1. Pain assessed with visual analog scale

    Time frame: Immediately before and immediately after the office-based ENT procedure during a single study visit

    Pain assessed on VAS (visual analog scale of 0-100 mm)

  2. Anxiety assessed with subjective units of distress scale

    Time frame: Immediately before and immediately after the office-based ENT procedure during a single study visit

    Anxiety assessed using Subjective Units of Distress scale (0-100)

Secondary outcomes

  1. Clinician experience with VR use

    Time frame: Immediately after the office-based ENT procedure during a single study visit

    Clinician experience with VR use assessing feasability and observed patient comfort using 7-point Likert scale

Other outcomes

  1. Patient satisfaction with VR use

    Time frame: Immediately after the office-based ENT procedure during a single study visit

    Patient satisfaction with VR use will be assessed using 7-point Likert scale for satisfaction and 5 brief multiple-choice experience questions

Study contacts

Contact information is provided by the study sponsor or research team.

Dennis M Tang, MD

CONTACT

[email protected]

310-423-1220

Sponsors and collaborators

Lead sponsor

Cedars-Sinai Medical Center

Other

Registry information

Official study title

Active vs. Passive Virtual Reality for Reducing Pain and Anxiety During Office-based ENT Procedures

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
May 20, 2026
Registry last updated
May 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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