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Pain Procedures and Anxiolysis Via Distraction With Virtual Reality

NCT04437173 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 99

Last updated 2022-09-28

No results posted yet for this study

Summary

The purpose of this study is to evaluate the efficacy of VR distraction on reducing anxiety patients undergoing interventional pain procedures compared to placebo/active placebo or a non VR option.

Conditions

Interventions

DEVICE

Virtual Reality Headset Distraction

Patient wears a virtual reality headset during interventional pain procedure

Sponsors & Collaborators

  • University of California, Davis

    lead OTHER

Principal Investigators

  • Naileshni Singh, MD · University of California, Davis

  • John Sun, MD · University of California, Davis

  • Michael Jung, MD · University of California, Davis

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-08-07
Primary Completion
2022-02-09
Completion
2022-02-09

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04437173 on ClinicalTrials.gov