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Virtual Occupational Therapy Application

Virtual Occupational Therapy Application

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02706912
Acronym
VOTA
Enrollment
22
Registered
2016-03-11
Start date
2016-02-29
Completion date
2017-02-28
Last updated
2017-08-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemiparesis, Stroke

Keywords

Stroke, Hemiparesis, Activities of Daily Living, Virtual World, Occupational Therapy

Brief summary

Virtual Occupational Therapy Application (VOTA) combines low-cost human motion tracking, commercial game engine technology, and evidence-based Occupational Therapy (OT) practice in a computer-based virtual world in which stroke patients practice activities of daily living (ADLs). The protocol investigates the efficacy of VOTA therapy for Upper Extremity (UE) motor recovery and assesses system usability and user acceptance.

Interventions

BEHAVIORALVOTA Therapy

During sessions of approximately one hour in duration, participants practice performing virtual activities of daily living (ADLs) using the VOTA system. During this practice, the participant's real-world motion is replicated by an avatar's motion in the virtual world. To complete the activities, participant's must perform a wide range of functional arm movements while interacting with virtual objects. Individuals are asked to perform three such one-hour virtual ADL practice sessions per week over a participation period of approximately eight weeks.

Sponsors

University of Virginia
CollaboratorOTHER
Barron Associates, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Participant is a hemiparetic stroke survivor; * Time since last stroke at least 3 months; * Participant has antigravity strength at the elbow to at least 45 degrees of active flexion in the stroke affected arm; * Participant has antigravity shoulder strength to at least 30 degrees each in active flexion, abduction/adduction, and 15 degrees in active rotation from an upright seated position in the stroke affected arm; * Participant has visual acuity with corrective lenses of 20/50 or better;

Exclusion criteria

* Existing participation in an upper extremity stroke rehabilitation program or planned participation during the study period; * Inability to understand and follow verbal directions; * Determination that participation would result in over exertion or significant discomfort or pain; * Determination that participation would result in significant agitation or elevated stress; * Withholding or withdrawal of consent by the participant; * Visual field deficit in either eye that impairs the ability to view the computer monitor; * Hemispatial neglect that impairs the ability process and perceive visual stimuli provided through the computer monitor;

Design outcomes

Primary

MeasureTime frameDescription
Fugl-Meyer upper extremity assessmentPre-assessment and Post-assessment (8 weeks)Measure of upper extremity motor function

Secondary

MeasureTime frameDescription
Wolf Motor Function TestPre-assessment and Post-assessment (8 weeks)Measure of upper extremity motor function
Repeatable Battery for the Assessment of Neuropsychological Status (RBANS)Pre-assessment and Post-assessment (8 weeks)Cognitive assessment
Trail Making TestPre-assessment and Post-assessment (8 weeks)Cognitive assessment

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026