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OpenTrials
Completed

NCT Number: NCT04245475

Water-friendly Virtual Reality and Brief Thermal Pain

Using immersive virtual reality as a form of pain distraction during a brief "painful but tolerable" temperature.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Washington (public not eligible for participation)

Seattle, Washington, 98195, United States

About this study

This study will use Quantitative Sensory Testing (computer-controlled brief 10 second thermal pain stimuli) in healthy college students.

The primary aim is to conduct a randomized, controlled study with healthy volunteers to explore whether interacting with virtual objects in VR via a high tech interactive VR system makes VR significantly more effective/powerful compared to a less immersive passive VR system, vs. No VR, for reducing pain during quantitative sensory testing.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Currently enrolled in a course at the University of Washington Psychology Dept., participating in the UW Psychology subject pool
  • Able to read, write and comprehend English
  • Able to complete study measures
  • Willing to follow our UW approved instructions
  • 18 years of age or older

Exclusion criteria

  • People how have already previously participated in this same study (e.g., last quarter) are not eligible to participate again.
  • Not enrolled in a course at the University of Washington Psychology Dept., participating in the UW Psychology subject pool
  • Not be able to read, write and comprehend English
  • Younger than 18 years of age.
  • Not capable of completing measures
  • Not capable of indicating pain intensity,
  • Not capable of filling out study measures,
  • Extreme susceptibility to motion sickness,
  • Seizure history,
  • Unusual sensitivity or lack of sensitivity to pain,
  • Sensitive skin,
  • sensitive feet,
  • migraines,
  • Diabetes.

Treatment and study plan

Virtual Reality psychological pain reduction

Behavioral

attention distraction

Primary outcomes

  1. participants rating of "worst pain "

    Time frame: immediately after each single 10 second test phase quantitative sensory test stimulus during a single visit

    using a single graphic rating scale, 0 = no pain, 10 = excruciating pain

Secondary outcomes

  1. participants rating of "time spent thinking about pain"

    Time frame: immediately after each single 10 second quantitative sensory test stimulus during a single visit

    using a single graphic rating scale, 0 = none of the time, 10 = all of the time

  2. participants rating of "pain unpleasantness "

    Time frame: immediately after each single 10 second quantitative sensory test stimulus during a single visit

    using a single graphic rating scale, 0 = no pain, 10 = excruciating pain

Other outcomes

  1. participants rating of "fun"

    Time frame: immediately after each single 10 second quantitative sensory test stimulus during a single visit

    using a single graphic rating scale, 0 = no fun, 10 = extremely fun.

Sponsors and collaborators

Lead sponsor

University of Washington

Other

Collaborators

  • National Institute of General Medical Sciences (NIGMS)

Registry information

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Jan 29, 2020
Registry last updated
Oct 26, 2021

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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