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Utilizing Gaming Mechanics to Optimize Telerehabilitation Adherence in Persons With Stroke

Primary Purpose

Stroke

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Home Telerehabilitation using HoVRS
Sponsored by
Rutgers, The State University of New Jersey
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring Stroke, Upper extremity, Hand, Arm, Virtual reality, Telerehabilitation, Gaming, Hemiparesis, Dexterity

Eligibility Criteria

40 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. unilateral stroke
  2. score of 22 or greater on the Montreal Cognitive Assesment
  3. Score of 1 or better on extinction and inattention portion of NIH Stroke Scale
  4. Fugl-Meyer (FM) between 36-58/66 (
  5. Score of 1 or better on language portion of NIHSS
  6. intact cutaneous sensation (ability to detect <4.17 Newton stimulation using Semmes-Weinstein nylon filaments)

Exclusion Criteria:

Orthopedic issues that would limit the ability to perform regular upper extremity activity

Sites / Locations

  • Rutgers The State University of New Jersey

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Home Telerehabilitation_Motivation Enhanced HTme

Home Telerehabilitation_Unenhanced (HTu)

Arm Description

The Home Telerehabilitation Motivation Enhanced (HTme) group will use the NJIT-HoVRS system to play a series of three games to train movement of their shoulder, elbow, wrist and fingers. The study team will set up the apparatus in their home at the initial visit and train them to use the system. After this, subjects will practice in their homes with on-line or in-person support as needed (once a week in person for the first month, and then an average of two times per month in person and two times per month on line). Subjects will be instructed to perform three of the simulations assigned to them as much as possible, but at least twenty minutes, daily for twelve weeks. The HTme group will use three simulations that will provide the user with eight to twelve levels of gradually increasing difficulty and complexity. A screen announces each level change and the graphics for each new level change substantially. Scoring opportunities increase at each new level.

The Home Telerehabilitation Motivation Enhanced (HTu) group will use the NJIT-HoVRS system to play a series of three games to train movement of their shoulder, elbow, wrist and fingers. The study team will set up the apparatus in their home at the initial visit and train them to use the system. After this, subjects will practice in their homes with on-line or in-person support as needed (once a week in person for the first month, and then an average of two times per month in person and two times per month on line). Subjects will be instructed to perform three of the simulations assigned to them as much as possible, but at least twenty minutes, daily for twelve weeks. The HTu group will use three simulations. Difficulty will be increased utilizing an adaptive control algorithm that increases difficulty based on performance. Difficulty changes are extremely incremental making them imperceptible for most subjects. Graphics and scoring do not change as difficulty level changes.

Outcomes

Primary Outcome Measures

Total intervention time
Total intervention time performed by patient during study period
Upper extremity Fugl Meyer Assessment
Behavioral test of upper extremity motor function
Upper extremity Fugl Meyer Assessment
Behavioral test of upper extremity motor function
Upper extremity Fugl Meyer Assessment
Behavioral test of upper extremity motor function
Intrinsic Motivation Inventory
Survey examining subjective response to rehabilitation program
Intrinsic Motivation Inventory
Survey examining subjective response to rehabilitation program

Secondary Outcome Measures

Number of intervention days
Number of self-initiated intervention days performed by patient during study period
Average intervention time per intervention day
Average intervention time performed by the subject
Action Research Arm Test
Behavioral test of upper extremity motor function
Action Research Arm Test
Behavioral test of upper extremity motor function
Action Research Arm Test
Behavioral test of upper extremity motor function
Box and Blocks Test
Behavioral test of upper extremity motor function
Box and Blocks Test
Behavioral test of upper extremity motor function
Box and Blocks Test
Behavioral test of upper extremity motor function
Nine Hole Peg Test
Behavioral test of upper extremity motor function
Nine Hole Peg Test
Behavioral test of upper extremity motor function
Nine Hole Peg Test
Behavioral test of upper extremity motor function
Stroke Impact Scale - Activities of Daily Living Subscale
Fifty point subscale. Higher score = better recovery. Subscales reported individually.
Stroke Impact Scale - Activities of Daily Living Subscale
Fifty point subscale. Higher score = better recovery. Subscales reported individually.
Stroke Impact Scale - Activities of Daily Living Subscale
Fifty point subscale. Higher score = better recovery. Subscales reported individually.
Stroke Impact Scale - Hand Subscale
Twenty five point subscale. Higher score = better recovery. Subscales reported individually.
Stroke Impact Scale - Hand Subscale
Twenty five point subscale. Higher score = better recovery. Subscales reported individually.
Stroke Impact Scale - Hand Subscale
Twenty five point subscale. Higher score = better recovery. Subscales reported individually.
Stroke Impact Scale - Participation Subscale
Forty point subscale. Higher score = better recovery. Subscales reported individually.
Stroke Impact Scale - Participation Subscale
Forty point subscale. Higher score = better recovery. Subscales reported individually.
Stroke Impact Scale - Participation Subscale
Forty point subscale. Higher score = better recovery. Subscales reported individually.
Stroke Impact Scale - Recovery Subscale
One hundred point subscale. Higher score = better recovery. Subscales reported individually.
Stroke Impact Scale - Recovery Subscale
One hundred point subscale. Higher score = better recovery. Subscales reported individually.
Stroke Impact Scale - Recovery Subscale
One hundred point subscale. Higher score = better recovery. Subscales reported individually.
Hand opening/closing range of motion
Sum of maximum angular excursions of the paretic metacarpo-phalangeal (MCP), proximal inter-phalangeal(PIP) and distal inter-phalangeal joints (DIP) joints during a hand opening activity
Hand opening/closing range of motion
Sum of maximum angular excursions of the paretic metacarpo-phalangeal (MCP), proximal inter-phalangeal(PIP) and distal inter-phalangeal joints (DIP) joints during a hand opening activity
Hand opening/closing range of motion
Sum of maximum angular excursions of the paretic metacarpo-phalangeal (MCP), proximal inter-phalangeal(PIP) and distal inter-phalangeal joints (DIP) joints during a hand opening activity
Hand trace RMSE
Ability to control hand opening as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Hand trace RMSE
Ability to control hand opening as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Hand trace RMSE
Ability to control hand opening as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Wrist Trace RMSE
Ability to control wrist flexion and extension as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Wrist Trace RMSE
Ability to control wrist flexion and extension as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Wrist Trace RMSE
Ability to control wrist flexion and extension as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Horizontal shoulder and elbow trace RMSE
Ability to control shoulder and elbow as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Horizontal shoulder and elbow trace RMSE
Ability to control shoulder and elbow as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Horizontal shoulder and elbow trace RMSE
Ability to control shoulder and elbow as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Twenty four hour upper limb activity magnitude ratio
Participant will wear tri-axial accelerometers on both wrists for twenty four hours and upper limb magnitude ratio will be calculated and reported as per Bailey (2015). For each second of this twenty four hour period accelerations across the three axes are combined into a single vector magnitude value. Inactive non-paretic UE is assigned a vector magnitude of -7 when paretic UE is moving alone. Inactive paretic UE is assigned a vector magnitude of 7 when non-paretic UE is moving alone. Paretic wrist vector magnitude will be divided by non-paretic wrist vector magnitude for each second. These calculated values will be transformed using a natural logarithm to prevent skewness of positive, untransformed values. Median of these values for the twenty four hour period will be reported for each individual subject.
Twenty four hour upper limb activity magnitude ratio
Participant will wear tri-axial accelerometers on both wrists for twenty four hours and upper limb magnitude ratio will be calculated and reported as per Bailey (2015). For each second of this twenty four hour period accelerations across the three axes are combined into a single vector magnitude value. Inactive non-paretic UE is assigned a vector magnitude of -7 when paretic UE is moving alone. Inactive paretic UE is assigned a vector magnitude of 7 when non-paretic UE is moving alone. Paretic wrist vector magnitude will be divided by non-paretic wrist vector magnitude for each second. These calculated values will be transformed using a natural logarithm to prevent skewness of positive, untransformed values. Median of these values for the twenty four hour period will be reported for each individual subject.
Twenty four hour upper limb activity magnitude ratio
Participant will wear tri-axial accelerometers on both wrists for twenty four hours and upper limb magnitude ratio will be calculated and reported as per Bailey (2015). For each second of this twenty four hour period accelerations across the three axes are combined into a single vector magnitude value. Inactive non-paretic UE is assigned a vector magnitude of -7 when paretic UE is moving alone. Inactive paretic UE is assigned a vector magnitude of 7 when non-paretic UE is moving alone. Paretic wrist vector magnitude will be divided by non-paretic wrist vector magnitude for each second. These calculated values will be transformed using a natural logarithm to prevent skewness of positive, untransformed values. Median of these values for the twenty four hour period will be reported for each individual subject.
Twenty four hour upper limb activity magnitude ratio
Participant will wear tri-axial accelerometers on both wrists for twenty four hours and upper limb magnitude ratio will be calculated and reported as per Bailey (2015). For each second of this twenty four hour period accelerations across the three axes are combined into a single vector magnitude value. Inactive non-paretic UE is assigned a vector magnitude of -7 when paretic UE is moving alone. Inactive paretic UE is assigned a vector magnitude of 7 when non-paretic UE is moving alone. Paretic wrist vector magnitude will be divided by non-paretic wrist vector magnitude for each second. These calculated values will be transformed using a natural logarithm to prevent skewness of positive, untransformed values. Median of these values for the twenty four hour period will be reported for each individual subject.

Full Information

First Posted
April 26, 2019
Last Updated
July 7, 2023
Sponsor
Rutgers, The State University of New Jersey
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), New Jersey Institute of Technology
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1. Study Identification

Unique Protocol Identification Number
NCT03985761
Brief Title
Utilizing Gaming Mechanics to Optimize Telerehabilitation Adherence in Persons With Stroke
Official Title
Utilizing Gaming Mechanics to Optimize Telerehabilitation Adherence in Persons With Stroke
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Completed
Study Start Date
September 8, 2019 (Actual)
Primary Completion Date
July 1, 2023 (Actual)
Study Completion Date
July 1, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rutgers, The State University of New Jersey
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), New Jersey Institute of Technology

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This trial studies the impact of motivational strategies designed by the gaming industry on adherence to a home tele-rehabilitation program designed to improve hand function in persons with stroke. A growing literature suggests that the extended practice of challenging hand tasks can produce measurable changes in hand function in persons with stroke. Current health care delivery systems do not support this volume of directly supervised rehabilitation, making it necessary for patients to perform a substantial amount of activity at home, unsupervised. Unfortunately, adherence to unsupervised home exercise regimens is quite poor in this population. The investigator's goal is to assess the impact of several well-established game design strategies: 1) Scaffolded increases in game difficulty 2) In-game rewards 3) Quests with enhanced narrative. The investigator's will utilize these enhancements to study their impact on motivation to perform a tele-rehabilitation- based home exercise program, adherence to the program and changes in hand function. The proposed study will utilize a system of novel rehabilitation technologies designed to facilitate home exercise performance. Subjects will perform 3 simulated rehabilitation activities supported by a passive exoskeleton, an infrared camera and software that will allow subjects to exercise at home. The investigator's will investigate: 1) Differences in measures of motivation elicited by motivationally enhanced simulations and un-enhanced control versions.2) The impact of motivational enhancements on actual adherence to a tele-rehabilitation program in persons with stroke and 3) The impact of motivational enhancement on improvements in hand function achieved by these subjects. This proposal will address a critical gap in modern rehabilitation - adherence to autonomous rehabilitation programs. Patient participation in unsupervised rehabilitation is one of the assumptions underpinning our health care system. This said, no data collected to date supports that adherence is acceptable. The technology and methodology in this proposal are an important step towards leveraging extensive research and development done by the computer gaming industry into improved rehabilitation practice.
Detailed Description
Purpose/Specific Aims The overarching aim of this study is to provide a mechanism for patients to engage in progressive motor practice for a meaningful time period. The investigator's aim to improve on the positive outcomes demonstrated in patients in the chronic phase and the pilot work being done on patients in the acute in-patient phase post stroke to determine whether functional recovery can be further improved using a home based system. Aim 1: Evaluate compliance with Home-Telerehabilitation simulated hand/arm gaming activities and two computer game groups, one with motivation enhanced: Home Training Motivation Enhanced (HTme) simulations and one with non-enhanced simulations: Home Training Unenhanced (HTu) versions. Hypothesis: Participants in the HTme group will show significant compliance as compared to the control group (HTu). Aim 2: Evaluate the effectiveness of motivation enhanced HTme home-based virtually simulated hand/arm gaming activities for individuals with stroke as compared to a program unenhanced HTu versions of the same simulations. Hypothesis: Participants completing HTme training will exhibit significantly improved clinical, kinematic and neurophysiological outcomes as compared to the control group (HTu). Aim 3: Evaluate the impact of the motivation enhancements designed into computer games to provide a more enjoyable training experience. Hypothesis: Enjoyment of the games will be a more valid predictor of compliance than personal factors. Background and Significance Studies have shown that sustained hand rehabilitation training is important for continuous improvement and maintenance of function following a stroke. It is unimaginably difficult to pursue education, employment and community participation without being able to independently use one's hands. The primary goal of this study is to test an exciting new technology that can be easily used in the home for long-term hand and upper extremity training. Recovery of hand function post brain injury is particularly recalcitrant to currently available interventions. To date, the best efforts of groups studying traditionally presented as well as technology-based therapeutic interventions for the hemiplegic hand and arm have produced measurable changes in motor function and motor control but fall far short of major reductions in disability. If the amount of therapy is critical to rehabilitation, our current institutional limitations undermine the probabilities for successful outcomes. After discharge from the inpatient stay, access to rehabilitation therapy can be difficult for some patients. This is due in part to inadequate insurance, lack of transportation, and the patient's dependence on their caregiver. Having access to long-term rehabilitation training anywhere and at any time is necessary for sub-acute and chronic patients to continuously improve their functional abilities. Research Design and Methods This study will be a single blind randomized controlled trial. Subjects will be blinded to the purpose of the study. All outcome measures will be performed by a therapist blinded to group assignment. A controlled trial will be utilized to determine the additive effect of presenting rehabilitation activities in a virtual environment as compared to standard upper extremity exercise. The investigators will randomize subjects to treatment and control groups using a computerized random number generator. 3.1. Duration of Study Each subject will perform a pre-study evaluation, train using one of the protocols for three months, perform a post study evaluation as well as one and six month retention evaluations. 3.2 Study Sites Testing and initial training will take place in the Bergen Building of the Rutgers Biomedical and Health Sciences Campus in Newark. Home training will take place in subjects' homes. 3.3 Sample Size Justification The investigators will seek sufficient power to detect a clinically significant difference in the Wolf score changes in these two pre-planned, primary comparisons. To evaluate these effects of training, we will assume a power level of .8 and a significance level of 0.05. With presumed correlation among repeated measures of 0.1 and effect size of 0.3, a sample size of 25 subjects in each of the two groups (HTme and HTu) to observe a significant effect for the first comparison (G*Power, version 3.1.5) is necessary. Although the investigators will screen for patients with homogeneous impairments, by its nature stroke is an extremely variable condition. Due to possible subject attrition, the investigators will use a total of 30 subjects in each of the two groups. 3.4 Subject Recruitment Subjects will be recruited through flyers, stroke support groups, and clinician referrals. The investigators will assume that approximately 15-20% of the population will satisfy our inclusion criteria based on our previous experience with upper extremity rehabilitation in this population. Hence the investigators will approach 300 persons. 3.5 Consent Procedures Example: The study will be explained to the potential subject by the study staff, the consent will be read, and their questions will be answered. If participants wish to enroll, the subject will sign the consent form. The study staff obtaining consent will also sign and date the consent form, and a copy will be given to the subject sought from each prospective subject or the subject's legally authorized representative, in accordance with federal & state law and institutional policy. If the study staff member performing the consent process identifies issues suggesting that the prospective subject may not be capable of participating in the consent process due to dementia, a Folstein Mini Mental Status will be performed. Prospective subjects screening positive for dementia will not be included in the study. 3.5.1 Subject Costs and Compensation There are no costs for the subjects. The subjects will be paid 100$ at each of the retention tests. Study Variables 4.1 Independent Variables or Interventions The two computer game groups, Motivation Enhanced (HTme) and Motivation Non-Enhanced (HTu) will use the NJIT- Home Virtual Rehabilitation System (HoVRS) to play a series of computer games developed to practice movement of the hand and fingers. Subjects will first come into our lab, perform pre-tests as well as a pre-intervention training session. Then a physical therapist and engineer will set up the apparatus in subject's home and will train them on how to use the system and play the games in their home during the first week. The physical therapist and engineer will be in contact with subjects throughout the training and will visit subjects' homes as needed if problems are encountered. Additionally, the system allows the therapist to remotely monitor each day's activity. 4.1.1 Device Description NJIT HoVRS has two sub-systems to deliver home-based training: 1) a patient based platform to provide the training and 2) a server based online data logging and reporting system. In the patient's home, a cross platform virtual reality training application runs video games (developed in the Unity 3D game engine using the language C#) on their home computer. 4.1.11 Hardware The Leap Motion Controller (LMC) a commercially developed infrared tracking device developed for home video game control is used to capture motion of the hand and arm movement without requiring wearable sensors. The device's USB controller reads the sensor data into its own local memory and performs any necessary resolution adjustments. This data is then streamed via USB to the Leap Motion image Application Programming Interface (API). From there, we programmed the system to feed tracking data into virtual reality activities by calling the Leap Motion API. If the patient's arm is weak and cannot support the hand against gravity above the Leap Motion Controller, a commercially available, spring-based arm support, will be provided to the subject (Figure 1). The arm support provides 12 different levels of passive support allowing it to accommodate a wide range of patient sizes and strength levels. It requires a single setting that can be provided during the patient's initial evaluation 4.1.1.2 Software Patients will either use their own home computer or will be provided with a computer if needed. A user-friendly Graphic User Interface (GUI) lists all of the training activities allowing patients to choose which activity they want to begin with using just one mouse click. Currently twelve games have been developed, each one designed to focus on training a specific hand or arm movement such as wrist rotation or finger individuation. All games are downloadable via HoVRS website. 4.2 Dependent Variables: See Outcomes Measures 4.3 Risk of Harm There is less than minimal risk involved. The virtual reality (VR) experiments are non-invasive and pose no obvious risk. Transient fatigue of the hand and arm are possible, but this risk is not greater than that posed by normal daily activities following a stroke. 4.4 Potential for Benefit The benefits of taking part in this study may be: Patient may regain better use of their hand and arm. However, it is possible that patients might receive no direct personal benefit from taking part in this study. Data Handling and Statistical Analysis All efforts will be made to keep subjects' personal information confidential. All subject names will be removed from the data and the data will be tagged using a coded identification (ID) number. Demographic, clinical outcome and survey data will first be recorded on paper. All kinematic and computerized performance data will be collected on computer. These computer files will be identified by the coded subject ID number. All data will be transferred to an Excel spreadsheet with subjects identified by this same ID number. Spreadsheets will be stored on a drive that is password protected. Data will only be accessible to study staff and will be retained for seven years. The link between subject identity and subject ID number will be destroyed when data collection is completed. The primary outcome measures and all secondary outcome measures described above will be subjected to a repeated measured analysis of variance, with between-group factors Therapy Type (HTme, HTu) and within-group factor Test (Before, Post, One Month retention, Six Months Retention). Post-hoc analyses of the Therapy Type by Test interaction effects will focus on the Month 1 versus Month 6 comparison. The investigators will be quantifying training effects by comparing group means as well as by percent change in performance, and by comparing the recovery curves obtained from Tests 1-4. All clinical outcomes used are well established measures of upper extremity functional recovery with published minimum clinically important differences which will be used to evaluate the significance of our findings. 7. Reporting Results 7.1 Individual Results No disease screening data will be collected. Patient's changes on clinical tests will be shared with them during testing sessions. These sessions are conducted by licensed Physical Therapists who have training to help persons with stroke interpret clinical examination findings. 7.2 Aggregate Results Subjects will not be informed of aggregate findings. 7.3 Professional Reporting De-identified, aggregate findings will be published in professional journals and presented at scientific meetings.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
Stroke, Upper extremity, Hand, Arm, Virtual reality, Telerehabilitation, Gaming, Hemiparesis, Dexterity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Home Telerehabilitation_Motivation Enhanced HTme
Arm Type
Experimental
Arm Description
The Home Telerehabilitation Motivation Enhanced (HTme) group will use the NJIT-HoVRS system to play a series of three games to train movement of their shoulder, elbow, wrist and fingers. The study team will set up the apparatus in their home at the initial visit and train them to use the system. After this, subjects will practice in their homes with on-line or in-person support as needed (once a week in person for the first month, and then an average of two times per month in person and two times per month on line). Subjects will be instructed to perform three of the simulations assigned to them as much as possible, but at least twenty minutes, daily for twelve weeks. The HTme group will use three simulations that will provide the user with eight to twelve levels of gradually increasing difficulty and complexity. A screen announces each level change and the graphics for each new level change substantially. Scoring opportunities increase at each new level.
Arm Title
Home Telerehabilitation_Unenhanced (HTu)
Arm Type
Active Comparator
Arm Description
The Home Telerehabilitation Motivation Enhanced (HTu) group will use the NJIT-HoVRS system to play a series of three games to train movement of their shoulder, elbow, wrist and fingers. The study team will set up the apparatus in their home at the initial visit and train them to use the system. After this, subjects will practice in their homes with on-line or in-person support as needed (once a week in person for the first month, and then an average of two times per month in person and two times per month on line). Subjects will be instructed to perform three of the simulations assigned to them as much as possible, but at least twenty minutes, daily for twelve weeks. The HTu group will use three simulations. Difficulty will be increased utilizing an adaptive control algorithm that increases difficulty based on performance. Difficulty changes are extremely incremental making them imperceptible for most subjects. Graphics and scoring do not change as difficulty level changes.
Intervention Type
Behavioral
Intervention Name(s)
Home Telerehabilitation using HoVRS
Intervention Description
The Home Virtual Rehabilitation System (HoVRS) integrates a Leap Motion controller, a passive arm support and a suite of custom designed hand rehabilitation simulations. The Leap Motion provides camera based measurement of finger joint positions, allowing for integrated virtual arm and finger training. If the patient's arm is severely impaired, a forearm orthosis that counter-balances gravity to provide graded support to the arm during activity is issued to the subject. In this study, we utilize 3 task-based simulations that train hand manipulation and arm transport. One simulation trains hand opening integrated with pronation and supination, a second trains wrist movement, by presenting targets that subjects navigate a plane over and around buildings to collect, a third simulation, trains shoulder and elbow disassociation in a horizontal plane integrated with hand opening.
Primary Outcome Measure Information:
Title
Total intervention time
Description
Total intervention time performed by patient during study period
Time Frame
Day one through day ninety of intervention period
Title
Upper extremity Fugl Meyer Assessment
Description
Behavioral test of upper extremity motor function
Time Frame
One day prior to intervention
Title
Upper extremity Fugl Meyer Assessment
Description
Behavioral test of upper extremity motor function
Time Frame
One day after intervention
Title
Upper extremity Fugl Meyer Assessment
Description
Behavioral test of upper extremity motor function
Time Frame
One month after intervention
Title
Intrinsic Motivation Inventory
Description
Survey examining subjective response to rehabilitation program
Time Frame
First day intervention period
Title
Intrinsic Motivation Inventory
Description
Survey examining subjective response to rehabilitation program
Time Frame
Day 90 of intervention period
Secondary Outcome Measure Information:
Title
Number of intervention days
Description
Number of self-initiated intervention days performed by patient during study period
Time Frame
Day one through day ninety of intervention period
Title
Average intervention time per intervention day
Description
Average intervention time performed by the subject
Time Frame
Day one through day ninety of intervention period
Title
Action Research Arm Test
Description
Behavioral test of upper extremity motor function
Time Frame
1 day prior to intervention period.
Title
Action Research Arm Test
Description
Behavioral test of upper extremity motor function
Time Frame
1 day after intervention period.
Title
Action Research Arm Test
Description
Behavioral test of upper extremity motor function
Time Frame
1 month after intervention period.
Title
Box and Blocks Test
Description
Behavioral test of upper extremity motor function
Time Frame
1 day before intervention period.
Title
Box and Blocks Test
Description
Behavioral test of upper extremity motor function
Time Frame
1 day after intervention period.
Title
Box and Blocks Test
Description
Behavioral test of upper extremity motor function
Time Frame
1 month after intervention period.
Title
Nine Hole Peg Test
Description
Behavioral test of upper extremity motor function
Time Frame
1 day before intervention period.
Title
Nine Hole Peg Test
Description
Behavioral test of upper extremity motor function
Time Frame
1 day after intervention period.
Title
Nine Hole Peg Test
Description
Behavioral test of upper extremity motor function
Time Frame
1 month after intervention period.
Title
Stroke Impact Scale - Activities of Daily Living Subscale
Description
Fifty point subscale. Higher score = better recovery. Subscales reported individually.
Time Frame
1 day before intervention period.
Title
Stroke Impact Scale - Activities of Daily Living Subscale
Description
Fifty point subscale. Higher score = better recovery. Subscales reported individually.
Time Frame
1 day after intervention period.
Title
Stroke Impact Scale - Activities of Daily Living Subscale
Description
Fifty point subscale. Higher score = better recovery. Subscales reported individually.
Time Frame
1 month after intervention period.
Title
Stroke Impact Scale - Hand Subscale
Description
Twenty five point subscale. Higher score = better recovery. Subscales reported individually.
Time Frame
1 day before intervention period.
Title
Stroke Impact Scale - Hand Subscale
Description
Twenty five point subscale. Higher score = better recovery. Subscales reported individually.
Time Frame
1 day after intervention period.
Title
Stroke Impact Scale - Hand Subscale
Description
Twenty five point subscale. Higher score = better recovery. Subscales reported individually.
Time Frame
1 month after intervention period.
Title
Stroke Impact Scale - Participation Subscale
Description
Forty point subscale. Higher score = better recovery. Subscales reported individually.
Time Frame
1 day before intervention period.
Title
Stroke Impact Scale - Participation Subscale
Description
Forty point subscale. Higher score = better recovery. Subscales reported individually.
Time Frame
1 day after intervention period.
Title
Stroke Impact Scale - Participation Subscale
Description
Forty point subscale. Higher score = better recovery. Subscales reported individually.
Time Frame
1 month after intervention period.
Title
Stroke Impact Scale - Recovery Subscale
Description
One hundred point subscale. Higher score = better recovery. Subscales reported individually.
Time Frame
1 day before intervention period.
Title
Stroke Impact Scale - Recovery Subscale
Description
One hundred point subscale. Higher score = better recovery. Subscales reported individually.
Time Frame
1 day after intervention period.
Title
Stroke Impact Scale - Recovery Subscale
Description
One hundred point subscale. Higher score = better recovery. Subscales reported individually.
Time Frame
1 month after intervention period.
Title
Hand opening/closing range of motion
Description
Sum of maximum angular excursions of the paretic metacarpo-phalangeal (MCP), proximal inter-phalangeal(PIP) and distal inter-phalangeal joints (DIP) joints during a hand opening activity
Time Frame
1 day before intervention period.
Title
Hand opening/closing range of motion
Description
Sum of maximum angular excursions of the paretic metacarpo-phalangeal (MCP), proximal inter-phalangeal(PIP) and distal inter-phalangeal joints (DIP) joints during a hand opening activity
Time Frame
1 day after intervention period.
Title
Hand opening/closing range of motion
Description
Sum of maximum angular excursions of the paretic metacarpo-phalangeal (MCP), proximal inter-phalangeal(PIP) and distal inter-phalangeal joints (DIP) joints during a hand opening activity
Time Frame
1 month after intervention period.
Title
Hand trace RMSE
Description
Ability to control hand opening as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Time Frame
1 day before intervention period.
Title
Hand trace RMSE
Description
Ability to control hand opening as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Time Frame
1 day after intervention period.
Title
Hand trace RMSE
Description
Ability to control hand opening as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Time Frame
1 month after intervention period.
Title
Wrist Trace RMSE
Description
Ability to control wrist flexion and extension as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Time Frame
1 day before intervention period.
Title
Wrist Trace RMSE
Description
Ability to control wrist flexion and extension as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Time Frame
1 day after intervention period.
Title
Wrist Trace RMSE
Description
Ability to control wrist flexion and extension as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Time Frame
1 month after intervention period.
Title
Horizontal shoulder and elbow trace RMSE
Description
Ability to control shoulder and elbow as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Time Frame
1 day before intervention period.
Title
Horizontal shoulder and elbow trace RMSE
Description
Ability to control shoulder and elbow as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Time Frame
1 day after intervention period.
Title
Horizontal shoulder and elbow trace RMSE
Description
Ability to control shoulder and elbow as subject moves a cursor tracking a sine wave. Reported as root mean square error (RMSE) comparing target position and cursor position.
Time Frame
1 month after intervention period.
Title
Twenty four hour upper limb activity magnitude ratio
Description
Participant will wear tri-axial accelerometers on both wrists for twenty four hours and upper limb magnitude ratio will be calculated and reported as per Bailey (2015). For each second of this twenty four hour period accelerations across the three axes are combined into a single vector magnitude value. Inactive non-paretic UE is assigned a vector magnitude of -7 when paretic UE is moving alone. Inactive paretic UE is assigned a vector magnitude of 7 when non-paretic UE is moving alone. Paretic wrist vector magnitude will be divided by non-paretic wrist vector magnitude for each second. These calculated values will be transformed using a natural logarithm to prevent skewness of positive, untransformed values. Median of these values for the twenty four hour period will be reported for each individual subject.
Time Frame
Between 96 and 72 hours prior to pretest
Title
Twenty four hour upper limb activity magnitude ratio
Description
Participant will wear tri-axial accelerometers on both wrists for twenty four hours and upper limb magnitude ratio will be calculated and reported as per Bailey (2015). For each second of this twenty four hour period accelerations across the three axes are combined into a single vector magnitude value. Inactive non-paretic UE is assigned a vector magnitude of -7 when paretic UE is moving alone. Inactive paretic UE is assigned a vector magnitude of 7 when non-paretic UE is moving alone. Paretic wrist vector magnitude will be divided by non-paretic wrist vector magnitude for each second. These calculated values will be transformed using a natural logarithm to prevent skewness of positive, untransformed values. Median of these values for the twenty four hour period will be reported for each individual subject.
Time Frame
Between 48 and 24 hours prior to pretest
Title
Twenty four hour upper limb activity magnitude ratio
Description
Participant will wear tri-axial accelerometers on both wrists for twenty four hours and upper limb magnitude ratio will be calculated and reported as per Bailey (2015). For each second of this twenty four hour period accelerations across the three axes are combined into a single vector magnitude value. Inactive non-paretic UE is assigned a vector magnitude of -7 when paretic UE is moving alone. Inactive paretic UE is assigned a vector magnitude of 7 when non-paretic UE is moving alone. Paretic wrist vector magnitude will be divided by non-paretic wrist vector magnitude for each second. These calculated values will be transformed using a natural logarithm to prevent skewness of positive, untransformed values. Median of these values for the twenty four hour period will be reported for each individual subject.
Time Frame
Between 24 and 48 hours after to post-test
Title
Twenty four hour upper limb activity magnitude ratio
Description
Participant will wear tri-axial accelerometers on both wrists for twenty four hours and upper limb magnitude ratio will be calculated and reported as per Bailey (2015). For each second of this twenty four hour period accelerations across the three axes are combined into a single vector magnitude value. Inactive non-paretic UE is assigned a vector magnitude of -7 when paretic UE is moving alone. Inactive paretic UE is assigned a vector magnitude of 7 when non-paretic UE is moving alone. Paretic wrist vector magnitude will be divided by non-paretic wrist vector magnitude for each second. These calculated values will be transformed using a natural logarithm to prevent skewness of positive, untransformed values. Median of these values for the twenty four hour period will be reported for each individual subject.
Time Frame
Between 72 and 96 hours after to post-test
Other Pre-specified Outcome Measures:
Title
Patient experience with HoVRS training
Description
Qualitative data related to subjects experience during the testing and training periods will be collected using a structured interview.
Time Frame
Interview will be conducted 30 days immediately after the intervention period.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: unilateral stroke score of 22 or greater on the Montreal Cognitive Assesment Score of 1 or better on extinction and inattention portion of NIH Stroke Scale Fugl-Meyer (FM) between 36-58/66 ( Score of 1 or better on language portion of NIHSS intact cutaneous sensation (ability to detect <4.17 Newton stimulation using Semmes-Weinstein nylon filaments) Exclusion Criteria: Orthopedic issues that would limit the ability to perform regular upper extremity activity
Facility Information:
Facility Name
Rutgers The State University of New Jersey
City
Newark
State/Province
New Jersey
ZIP/Postal Code
07107
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Immediately following completion of our proposed study we will submit a de-identified data set our protocol and links to published papers based on the data set to the Centralized Open Access Rehabilitation Data Base for Stroke (SCOAR).
IPD Sharing Time Frame
We will make our data available immediately after study completion. Data will remain available indefinitely.
IPD Sharing Access Criteria
Not Applicable - Open Access
IPD Sharing URL
http://keithlohse.github.io/SCOAR_data_viz/#
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Utilizing Gaming Mechanics to Optimize Telerehabilitation Adherence in Persons With Stroke

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