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Robot Assisted Virtual Rehabilitation for the Hand Post Stroke (RAVR)

Optimizing Hand Rehabilitation Post Stroke Using Interactive Virtual Environments

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03569059
Acronym
RAVR
Enrollment
115
Registered
2018-06-26
Start date
2018-08-24
Completion date
2024-08-15
Last updated
2024-10-03

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

Conditions

Stroke, Acute

Keywords

Stroke, Virtual Environment, Robotics, Upper Extremity, Hand, Transcranial Magnetic Stimulation

Brief summary

This study investigates the effects of intensive, high dosage task and impairment based training of the hemiparetic hand, using haptic robots integrated with complex gaming and virtual reality simulations. There is a time-limited period of post-ischemic heightened neuronal plasticity during which intensive training may optimally affect the recovery of motor skills, indicating that the timing of rehabilitation is as important as the dosing. However, recent literature indicates a controversy regarding both the value of intensive, high dosage as well as the optimal timing for therapy in the first two months after stroke. This study is designed to empirically investigate this controversy. It is evident that providing additional, intensive therapy during the acute rehabilitation stay is more complicated to implement and difficult for patients to tolerate, than initiating it in the outpatient setting, immediately after discharge. The robotic/VR system is specifically designed to deliver hand and arm training when motion and strength are limited, using adaptive algorithms to drive individual finger movement, gain adaptation and workspace modification to increase finger and arm range of motion, and haptic and visual feedback from mirrored movements to reinforce motor networks in the lesioned hemisphere.

Detailed description

This study investigates the effects of high dosage task and impairment based training of the hemiparetic hand, using haptic robots integrated with complex gaming and virtual reality simulations on recovery and function of the hand, when the training is initiated within early period of heightened plasticity. The intervention uses two training systems. NJIT-RAVR consists of a data glove combined with the Haptic Master robot that provides tracking of movements in a 3D workspace and enables programmable haptic effects, such as variable anti-gravity support, springs and dampers, and various haptic objects. The NJIT-TrackGlove consists of a robotic hand exoskeleton to provide haptic effects or assistance and an instrumented glove for finger angle tracking, and an arm tracking system to track hand and arm position and orientation. Using programmable software and custom bracing we enable use of this system for patients with a broad set of impairments and functional abilities. A library of custom-designed impairment and task-based simulations that train arm transport and hand manipulation, together or separately will be used. Pilot data show that it is possible to integrate intensive, high-dosage, targeted hand therapy into the routine of an acute rehabilitation setting. The study integrates the behavioral, the kinematic/kinetic and neurophysiological aspects of recovery to determine: 1) whether early intensive training focusing on the hand will result in a more functional hemiparetic arm; (2) whether it is necessary to initiate intensive hand therapy during the very early inpatient rehabilitation phase or will comparable outcomes be achieved if the therapy is initiated right after discharge, in the outpatient period; and 3) whether the effect of the early intervention observed at 6 months post stroke can be predicted by the cortical reorganization evaluated immediately prior to the therapy. This study will fill critical gaps in the literature and make a significant advancement in the investigation of putative interventions for recovery of hand function in patients post-stroke.

Interventions

DEVICEEarly Robotic/VR Therapy (EVR)

Subjects will perform state-of-art inpatient usual care therapy. In addition, they will perform an extra 1-hour/day of intensive therapy focusing on the hand in the form of interactive virtual reality games while assisted by robots. This additional treatment will be initiated 5-30 days post stroke.

BEHAVIORALDose-Matched Usual Physical Therapy Care

Subjects will perform state-of-art usual physical/occupational care and 10 days of one additional hour of state-of-art usual inpatient and/or outpatient physical therapy/occupational therapy.

DEVICEDelayed Robotic/VR Therapy (DVR)

Subjects will perform state-of-art inpatient usual care therapy. In addition, they will perform an extra 1-hour/day of intensive therapy focusing on the hand in the form of interactive virtual reality games while assisted by robots. This additional treatment will be initiated 31-60 days post stroke.

Sponsors

Rutgers University
CollaboratorOTHER
Northeastern University
CollaboratorOTHER
Kessler Foundation
CollaboratorOTHER
New Jersey Institute of Technology
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Participants are assigned to one of four groups in parallel for the duration of the study.

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* unilateral right or left sided stroke within 7 to 30 days of starting study * sufficient cognitive function to follow instructions * Fugl-Meyer (FM) of ≤ 49/66 * intact cutaneous sensation (e.g. ability to detect \<4.17 N stimulation using Semmes- Weinstein nylon filaments

Exclusion criteria

* prior stroke with persistent motor impairment or other disabling neurologic condition * non-independent before stroke * receptive aphasia * hemispatial neglect or severe proprioceptive loss * significant illnesses * severe arthritis that limits arm and hand movements * a score of ≥1 on the NIHSS limb ataxia item

Design outcomes

Primary

MeasureTime frameDescription
Action Research Arm Test (ARAT)4 months post strokeThe ARAT assesses upper extremity activity. It is a 19 item test divided into four subscales: grasp, grip, pinch and movement. Scores range from 0-57 with higher scores indicating better performance.

Secondary

MeasureTime frameDescription
Cortical Area Representation of the Finger-Hand Muscles4 months post strokeSingle-pulse transcranial magnetic stimulation will be used to assay patterns of corticospinal reorganization. Changes in the ipsilesional hand cortical territory for all subjects will be quantified using motor evoked potentials. The topographic representation of the hand and arm muscles will be mapped.
EEG-Based Measure of Resting State Brain Connectivity4 months post strokeElectroencephalography will be used to evaluate resting-state brain connectivity.
EEG-Based Measure of Task-Based Brain Connectivity4 months post strokeTask-based connectivity will be evaluated.
Cerebral Oxygenation in Sensorimotor Cortex4 months post strokeFunctional near-infrared spectroscopy will be used to quantify cerebral oxygenation in the sensorimotor cortex during a simple motor task.
Blocks and Box Test4 months post strokeA unilateral test of manual dexterity scored as the maximum number of blocks that can be moved from one compartment of the box to another of equal size, within 60 seconds.
Fugl-Meyer Test of Sensorimotor Function After Stroke (UEFM)4 months post strokeAn impairment based measure consisting of 33 movements that tests motor and sensation of the affected arm. Higher scores indicate less impairment and more isolated motions.
Wolf Motor Function Test4 months post strokeA 15 item timed test of arm and hand use in patients post stroke. The items begin with simple proximal movements and progress to more complex distal hand movements.
Coordination between Hand Transport and Grasp during Reaching4 months post strokeThe real-world Reach-Grasp test measures the kinematics of everyday movements involving grasping and manipulating household objects. Kinematics of reaching for an object, lifting it from the support, transporting it to a predefined location and releasing the object will be evaluated. Coordination between hand transport and grasping will be evaluated by analyzing hand preshaping during reach.
Arm Range of Motion4 months post strokeActive range of motion for fingers, wrist, elbow and shoulder.
Accuracy of Tracking a Square and Sine Wave with Fingertip Pinch Force4 months post strokeAbility to regulate force will be evaluated by measuring the accuracy of tracking square and sine waves presented on a computer screen. Vertical position of the cursor on the screen will be defined by isometric force between the thumb and index fingertips measured by a force sensor.
Action Research Arm Test6 months post strokeThe ARAT assesses upper extremity activity. It is a 19 item test divided into four
Accuracy of Tracking a Square and Sine Wave with Isotonic Finger Flexion/Extension4 months post strokeA data glove will be used to evaluate the accuracy of tracking square and sine waves presented on a computer screen with isotonic finger flexion/extension. Vertical position of the cursor on the screen will be defined by the average of four metacarpophalangeal finger joints.
Measurement of Daily Use of Upper Extremity4 months post strokeWearable sensors will be used to quantify daily use of the affected arm after the intervention.
EuroQol4 months post strokeThe EuroQol - EQ-5D is a standardized instrument used as a measure of health-related quality of life. The descriptive system comprises five dimensions: 1. mobility, the person's walking ability; 2. self-care, the ability to wash or dress by oneself; 3. usual activities dimension, performance in work, study, housework, family or leisure activities; 4. pain/discomfort, how much pain or discomfort they have, and 5. anxiety/depression, how much anxious or depressed they are. The respondents self-rate their level of severity for each dimension.
National Institutes of Health Stroke Scale (NIHSS)4 months post strokeThe NIHSS is a 15-item neurologic examination stroke scale used to evaluate and document neurological status in stroke patients and the effect of acute cerebral infarction on the levels of consciousness, language, neglect, visual-field loss, extraocular movement, motor strength, ataxia, dysarthria, and sensory loss. Ratings for each item are scored with 3 to 5 grades with 0 as normal.
Change in Robot-Based Measure of Elbow-Shoulder Coordination during ReachingDay 1 and and Day 10 of treatment for EVR and DVR groupsTo compare the immediate effects of training in the EVR and DVR groups, subjects will reach to five haptically rendered spheres located in a 3D virtual environment. The test will be performed every day immediately prior to VR training to measure changes in patterns of elbow-shoulder coordination.
Change in Robot-Based Measure of Maximum Seated Workspace during ReachingDay 1 and and Day 10 of treatment for EVR and DVR groupsTo compare the immediate effects of training in the EVR and DVR groups, subjects will reach to five haptically rendered spheres located in a 3D virtual environment. The test will be performed every day immediately prior to VR training to measure changes in maximum seated workspace.
Change in Robot-Based Measure of Movement Speed during Arm ReachingDay 1 and and Day 10 of treatment for EVR and DVR groupsTo compare the immediate effects of training in the EVR and DVR groups, subjects will reach to five haptically rendered spheres located in a 3D virtual environment. The test will be performed immediately prior to VR training to measure changes in arm speed during reaching for a virtual target.
Change in Robot-Based Measure of Movement Speed during Targeted Finger MotionDay 1 and and Day 10 of treatment for EVR and DVR groupsTo compare the immediate effects of training in the EVR and DVR groups, subjects will perform targeted finger movements in a virtual environment. The test will be performed every day immediately prior to VR training to measure changes in the speed of finger movement towards a virtual target.
Patient's Structured Subjective AssessmentImmediately post treatment (ideally within 72 hours) for EVR and DVR groupsThis is a 27 item questionnaire that addresses the subjects perception of the function of their hemiplegic arm and the effect this intervention had on their hand function. Subjects fill out the questionnaire prior to and directly after the intervention. Some questions require a response such as disagree, neutral and agree, others require ordering their gaming activity preferences, or responding to a question with a short answer.
Maximum Thumb and Index Fingertip Pinch Force4 months post strokeA force sensor will be used to measure in Newtons maximum isometric pinch force achieved between the thumb and index fingertips.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026