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Pilot Study: VR Mind and VR Mind+ Intervention

NCT03647605 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2019-02-12

No results posted yet for this study

Summary

The aim of the pilot study is feasibility, usability and safety assessment of VR Mind intervention. In particular the subject of assessment will be:

* the length of the laboratory session utilizing virtual reality exposure (feasibility),
* the ergonomics and ease of use for both patients and system operators (usability),
* the frequency of side effect occurrence as a result of virtual reality exposure (ie. Vertigo) (safety).

The results pilot study will be used in the designing a clinical trial aimed for testing efficacy and safety of VR Mind intervention.

Conditions

  • Social Phobia

Interventions

BEHAVIORAL

VR Mind

Two VR Mind sessions using virtual reality scenarios concerning social situations in which social phobics are prone to experience anxiety. The pilot study will consist of two scenarios: "Public Speaking in Lecture Hall" and "Telephoning in Public". Two sessions are planned, each containing two expositions to virtual reality environment, each lasting 10 minutes.

Sponsors & Collaborators

  • National Center for Research and Development, Poland

    collaborator OTHER

  • Tomorrow Sp. z o.o.

    lead INDUSTRY

Principal Investigators

  • Paweł Mierzejewski, prof · Tomorrow Sp. z o.o.

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2018-09-13
Primary Completion
2019-01-31
Completion
2019-01-31

Countries

  • Poland

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 NCT03647605 on ClinicalTrials.gov