VR, Visio-tactile Stimulation and Embodiment

Sponsor
Tufts University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05836038
Collaborator
(none)
30
2
12

Study Details

Study Description

Brief Summary

Investigators will evaluate the feasibility of "puppeting" a virtual hand with the opposite hand in increasing complex movements and the effect of visio-tactile stimuli on embodiment to determine if it is a necessary part of the process.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Visio-Tactile Stimulation
N/A

Detailed Description

Embodiment refers to a subjective experience where a person views a simulated body and its properties are experienced as if they were the person's own biological body (1). Embodiment is notably seen in the rubber hand illusion (2): a rubber hand is made to substitute for the real hand using visio-tactile stimulation to connect the rubber hand to the participant. In visio-tactile stimulation, the real hand is hidden from view and the rubber hand is positioned where the real hand should be. Both hands are simultaneously stroked while the participant views the rubber hand. Within a short time, the rubber hand "feels" touch and pain, independent of the real hand.

In this study investigators will evaluate the ability to enable embodiment in a virtual reality environment. After providing background information, participants will then complete the "Real Hand Session" of the Study Protocol (See below) using their real hand to move the same side virtual hand (e.g. left real hand movements will move left virtual hand). Participants will complete Usability and Embodiment /Presence surveys After the Actual Protocol, participants in the VTS group will receive visio-tactile stimuli. They will see their virtual hand touched while simultaneously feel their opposite real hand touched in the same pattern. Participants in the NoVTS will spend the same amount of time looking at their virtual hand without the touching (~1 minute).

For the "Puppet Session" participants will complete the same tasks as the "Real Hand Session"(See Below) but movement of the real hand will "puppet" the opposite virtual hand (right real hand movements will move left virtual hand). After completing the session participants will complete Usability and Embodiment /Presence surveys

Study Protocol Sessions.(20 to 30 minutes). All take place in the virtual environment Hand Movement- Press a 36-button sequence 4x Bilateral Task - "Catch" 36 "fireflies" with both hands 4x. Unilateral Task - "Catch 36 "fireflies" with one hand 4x. Avoidance Task - Press a 36-button sequence. A "dangerous" virtual obstacle (e.g., sawblade) will be placed in the path of the virtual hand during some of the trajectories. Investigators will see how far from the most efficient trajectory participants moves to avoid the object

Hypotheses H1: Participants will demonstrate a greater sense of embodiment with visio-tactile stimuli (VTS) than without visio-tactile stimuli (NoVTS) H1a: Participants in the VTS group will report higher levels of embodiment than those in the NoVTS group.

H1b: Participants will demonstrate significantly better motor performance in the VTS group than the NoVTS group.

H1c: Participants in the VTS group will demonstrate greater avoidance of "dangerous items" than those in the NoVTS group H1d: Participants in the VTS group will report better usability of the embodied virtual hand than those in the NoVTS group.

H2: Motor Performance of the "Puppeted" virtual hand will be similar to the "Actual" virtual hand.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Creating Embodiment in Virtual Reality: A Pilot Study Evaluating Visio-tactile Stimulation and Feasibility
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Jun 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Visio-tactile stimulation (VTS) during Virtual Reality

Participants in this group will receive visio-tactile stimulation prior to engaging with the VR program. They will see their virtual hand touched while simultaneously feel their opposite real hand touched in the same pattern.

Behavioral: Visio-Tactile Stimulation
They will see their virtual hand touched while simultaneously feel their opposite real hand touched in the same pattern.

No Intervention: No Visio-Tactile Stimulation (NoVTS) during Virtual Reality

Participants in this group will not receive visio-tactile stimulation prior to engaging with the VR program. They will be asked to look at their virtual hands for approximately the same amount of time as the VST group receive their stimulation

Outcome Measures

Primary Outcome Measures

  1. Motor Performance - Speed [Through study completion, 1 day]

    We will track and store participant movements during each task via the VR headset. These movements will be downloaded and processed to calculate speed

  2. Motor Performance - Velocity [Through study completion, 1 day]

    We will track and store participant movements during each task via the VR headset. These movements will be downloaded and processed to calculate velocity

  3. Motor Performance - Precision [Through study completion, 1 day]

    We will track and store participant movements during each task via the VR headset. These movements will be downloaded and processed to calculate Precision

  4. Motor Performance - Trajectory [Through study completion, 1 day]

    We will track and store participant movements during each task via the VR headset. These movements will be downloaded and processed to calculate trajectory

  5. Motor Performance - Path Length [Through study completion, 1 day]

    We will track and store participant movements during each task via the VR headset. These movements will be downloaded and processed to calculate path length

  6. Motor Performance - Time to Target [Through study completion, 1 day]

    We will track and store participant movements during each task via the VR headset. These movements will be downloaded and processed to calculate Time to target

  7. Motor Performance - Error rate [Through study completion, 1 day]

    We will track and store participant movements during each task via the VR headset. These movements will be downloaded and processed to calculate error rate

  8. Embodiment [Through study completion, 1 day]

    Participants perception of immersion during VR experience: Using Peck's Embodiment Scale (16 items scored on a 7 point likert scale with a final score between 1 and 7 with a higher score indicating greater emobidment) and the IPQ Presence questionnaire (14 items on a 7 point likert scale with a higher score indicating greater embodiment)

  9. Presence [Through study completion, 1 day]

    Participants perception of immersion during VR experience: IPQ Presence questionnaire (14 items on a 7 point likert scale with a score between 7 and 98 and a higher score indicating greater presence)

  10. Usability - Engagement [Through study completion, 1 day]

    Participants perception of the ease of use of the VR system using the User Engagement Scale (a 12 item 1-5 pt likert scale with scores between 12 and 60 and a higher score indicating greater usability)

  11. Usability - Task Demands [Through study completion, 1 day]

    Participants perception of the ease of use of the VR system using the NASA Task Index (6-item scored on 10 point VAS. Items are weighted by subject perception of what is important part of task. Higher score indicates greater task demand)

  12. Usability - ease of use [Through study completion, 1 day]

    Participants perception of the ease of use of the VR system using the System Usability Scale (10 item scored on 1-5 likert, scores are converted to a 100 scale with a higher score indicating greater ease of use)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • • 30 adult participants (18+)

  • Right Handed

Exclusion Criteria:
  • Seizure, loss of awareness, or other symptom linked to an epileptic condition in the last 5 years

  • Blind;

  • Unable to use hands to reach and grasp items

  • Implanted medical device such as a pacemaker, defibrillator, or hearing aid.

  • Contagious disorder on the face (such as pink eye) that could be transmitted via the VR head set or has open areas on the face or head that would come in contact with the headset;

  • Unable to understand and respond to English

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Tufts University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Nancy Baker, Associate Professor, Tufts University
ClinicalTrials.gov Identifier:
NCT05836038
Other Study ID Numbers:
  • HM&E123
First Posted:
May 1, 2023
Last Update Posted:
May 1, 2023
Last Verified:
Apr 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Nancy Baker, Associate Professor, Tufts University

Study Results

No Results Posted as of May 1, 2023