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Completed

NCT Number: NCT03104647

VRP-Clinic Software Evaluation - in Support of Rehabilitation (VRP02)

The current study is designed to evaluate neck movements performed according to the VRP-Clinic software, and to verify that they promote physical activities that correspond with physical rehabilitation.

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Key information

Conditions

Rehabilitation

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Shaare Zedek Medical Center

Jerusalem, 9103102, Israel

About this study

The study will take place at Shaare Zedek Medical Center (SZMC). The study will include a single visit.

Each subject will put on the VR headset and perform a series of neck movements guided by graphic instructions appearing in the VR environment. The session will be recorded with a video camera which will subsequently be viewed and evaluated by clinicians. The clinicians will identify each movement seen on the video from a predefined list and determine if such a movement is recommended as part of a rehabilitation training program.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy male or female
  • Age 18-65

Exclusion criteria

  • History of neck related disorders (Whiplash, disc degeneration disease or other acute cervical spine conditions)
  • Current neck pain
  • Under medical treatment or observation for any health-related issue during the study
  • Recent trauma
  • Oncology background
  • Acute disease/illness
  • Pregnancy.
  • Using drugs that could potentially affect physical function and balance (such as corticosteroids, antipsychotics or antidepressants)
  • Vision problems that require glasses (not all frame types can fit into the headset)

Treatment and study plan

VRP-Clinic

Other

Subjects will perform a series of neck movements guided by graphic instructions appearing in the virtual reality environment

Primary outcomes

  1. Number of VRP-Clinic Neck Movements That the Assessing Clinician Recognizes as Rehabilitation Movements

    Time frame: Up to 2 weeks after the session

    The movements are recorded on video and sent to clinicians for evaluation after the session is completed.

    The movements are then evaluated by the clinicians according to a predetermined list.

Secondary outcomes

  1. Number of Participants With Any Adverse Event Occurring During the Study

    Time frame: through study completion, an average of 2 weeks

    Safety measure - The number of participants with any adverse event reported by the subject or observed by the investigator/clinician during the study will be recorded.

Sponsors and collaborators

Lead sponsor

VRHealth Group Ltd

Industry

Collaborators

  • Shaare Zedek Medical Center

Registry information

Official study title

Evaluation of the Performance of VRP-Clinic in Healthy Subjects in the Support of Rehabilitation

Acronym: VRP02

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Apr 7, 2017
Registry last updated
Sep 25, 2018

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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