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Healthy Volunteer Undergoing Painful Stimuli With and Without Hypnosis and Virtual Reality

NCT04107558 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2022-09-30

No results posted yet for this study

Summary

The main purposes of this study are as follows:

Compare the effect of painful stimuli with and without Hypnosis and Virtual Reality (HVR) on healthy volunteers.

* Use of sensors and captors to monitor physiological and neurophysiological changes by painful stimulus
* Monitor level of pain and anxiety with and without HVR
* Monitor level of unpleasantness of the pain with and without HVR
* Monitor level of Anxiety, Absorption, Dissociation, Satisfaction and Comfort with and without HVR

Conditions

  • Digital Sedation

Interventions

DEVICE

Virtual Reality

Subjects will undergo painful stimuli without HVR followed by a session with HVR. Subjects are their own control

Sponsors & Collaborators

  • University of Liege

    collaborator OTHER

  • Oncomfort

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-09-02
Primary Completion
2020-01-21
Completion
2022-08-30

Countries

  • Belgium

Study Locations

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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 NCT04107558 on ClinicalTrials.gov