Skip to main content
OpenTrials
Completed

NCT Number: NCT05846464

Virtual Reality to Enhance Upper Extremity Physical Therapy and Recovery

This is a descriptive study assessing the feasibility of using VR rehabilitation with unilateral (or bilateral) impairment of the arm, wrist and or hand resulting in reduced range of motion, dexterity, and/or strength of the hand.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Walter Reed National Military Medical Center

Bethesda, Maryland, 20814, United States

About this study

The purpose of this study is to determine the feasibility of using a virtual reality program to monitor and encourage compliance with musculoskeletal home exercise programs. It hypothesizes that the treatment will display improved compliance, range of motion, and general function for individuals with upper extremity musculoskeletal deficits.

The primary objectives are to: 1. Describe participant compliance with an immersive game-based virtual reality (VR) rehabilitation device for delivering at-home occupational therapy exercises for the wrist and hand in individuals with motor impairments. 2. Describe and compare functional outcomes among participants before and after completing at-home rehabilitation using the VR system.

These objective outcomes will be measured through various standardized tests completed by qualified study team members.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • DoD Beneficiary
  • Exhibiting musculoskeletal impairment requiring continued at-home rehabilitation
  • Cleared by research or clinical medical provider for participation
  • Participant no longer has active range of motion movement restrictions. They may still have weight bearing restrictions but nothing that will preclude them from moving their hand and digits to their maximum ability.
  • Ability to keep hand and arm in the field of view of the VR scene
  • Must have demonstrated the ability for the Oculus to track all hand and wrist motions of interest (during an initial screening at baseline)
  • Ability to independently don and doff the VR headset, plus start the app (verified in the Occupational Therapy/Physical Therapy clinic)
  • Age range between 18-65
  • Demonstrate the ability to tolerate wearing the VR headset

Exclusion criteria

  • History of photo-induced seizures
  • History of motion sickness when using VR equipment (especially vestibular effects such as nausea, dizziness, etc.)
  • Partial amputations of the arm being assessed (including missing digits as they may not enable tracking by the VR)

Treatment and study plan

Meta Quest 2

Device

The Meta/Oculus Quest (along with the SignWave software) delivers an immersive audio/visual-based game environment where the users hand is created and displayed in the virtual environment and matches target gestures to the beat of the music.

Primary outcomes

  1. Jebsen-Taylor Hand Function Test

    Time frame: 30 minutes

    Assessment of functional use and selection of appropriate grasp for common activities of daily living

Secondary outcomes

  1. 9-hole Peg Test

    Time frame: 10 minutes

    Speed and accuracy of grasp and release

  2. Hand/wrist goniometric range of motion (ROM)

    Time frame: 15 minutes

    Hand/wrist range of motion assessment

Other outcomes

  1. Quick DASH (Disabilities of the Arm, Shoulder and Hand) Questionnaire

    Time frame: 5 minutes

    Self-reported perception of functional ability of arm, shoulder, and hand

  2. NASA-TLX

    Time frame: 5 minutes

    Ease of use preference and mental load survey

  3. System Usability Scale

    Time frame: 2 minutes

    Quantitative ease of use assessment

  4. Open-Ended Usability Scale

    Time frame: 2 minutes

    Qualitative ease of use assessment

Sponsors and collaborators

Lead sponsor

Henry M. Jackson Foundation for the Advancement of Military Medicine

Other

Collaborators

  • Johns Hopkins University
  • Walter Reed National Military Medical Center

Registry information

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
May 6, 2023
Registry last updated
Mar 14, 2025

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.