National Fully Remote Use of IpsiHand Device in Hemiparetic Stroke

• Sponsor: Neurolutions, Inc. (Industry)
• Overall Status: Not yet recruiting
• CT.gov ID: NCT05965713
• Collaborator: Washington University School of Medicine (Other)
• Enrollment: 80
• Location: 1
• Arms: 2
• Anticipated Duration (Months): 18
• Patients Per Site Per Month: 4.5

Study Details

Study Description

Brief Summary

The goal of this study is to define the efficacy of fully remote home-based BCI therapy in chronic hemiparetic subcortical stroke patients. A randomized controlled study using the integrated remote BCI system will be tested against standard exercise therapy to determine the efficacy of motor improvement in chronic stroke patients with an upper extremity hemiparesis. Specifically, the integrated BCI system will include 1) the remote screening and motor assessment system for the upper extremity and 2) the BCI-controlled robotic hand exoskeleton (i.e. IpsiHand).

Condition or Disease	Intervention/Treatment	Phase
Stroke; Hemiparesis; Spasticity as Sequela of Stroke; Brain Computer Interface	Device: Neurolutions IpsiHand System; Other: Standard of Care - Home Exercise Program for Upper Extremity	N/A

Detailed Description

The ultimate goal of this project is to develop a functioning and clinically feasible method for restoring function to motor impaired stroke survivors. This ultimate goal is to develop a system that allows for enhanced functional capability and works consistently over a long-term basis and is accessible remotely no matter location or access to healthcare. In developing a new rehabilitation method, the researchers hope to create a system that allows for closed loop feedback through a robotic hand orthosis on the motor impaired side of stroke patients in response to intended movements of the muscles. The method, if successful, would represent an ideal, non-invasive method of promoting motor learning and recovery in stroke survivors. The ability to operate robotic hand orthosis using electrical signals of the brain is rapidly leaving the realm of science fiction and becoming a realistic goal of the clinical community. The current advances in BCI controlled neuroprosthetics could have immeasurable influence on adult patients with severe motor impairments from stroke. Even further on the horizon the insights developed from such work could substantively alter the way all stroke patients are treated and rehabilitated.

Study Design

• Study Type: Interventional
• Anticipated Enrollment: 80 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Intervention Model Description: Study staff will screen participants virtually or in person for eligibility after completing the informed consent process and documentation. After screening for study eligibility has occurred, the initial EEG screening will take place for all individuals who meet the criteria for the study as to ensure no preference to subjects with optimal signals for use of the IpsiHand. Once EEG screenings have been completed, the participant will be randomly assigned to Group 1 (BCI treatment) or Group 2 (standard of care treatment group). Each group will complete a daily therapy regimen. In Group 1 (BCI group)- will complete daily BCI therapy. In Group 2 (standard of care)- individuals will complete standard of care therapy program daily for 12 weeks provided by an occupational therapist.Study staff will screen participants virtually or in person for eligibility after completing the informed consent process and documentation. After screening for study eligibility has occurred, the initial EEG screening will take place for all individuals who meet the criteria for the study as to ensure no preference to subjects with optimal signals for use of the IpsiHand. Once EEG screenings have been completed, the participant will be randomly assigned to Group 1 (BCI treatment) or Group 2 (standard of care treatment group). Each group will complete a daily therapy regimen. In Group 1 (BCI group)- will complete daily BCI therapy. In Group 2 (standard of care)- individuals will complete standard of care therapy program daily for 12 weeks provided by an occupational therapist.
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: IpsiHand Device Use in Hemiparetic Stroke Population to Assess Home Based EEG System Candidacy for BCI Rehabilitation of the Upper Extremity and the Efficacy of a Full Remote Home Based BCI Therapy - A Randomized Control Trial
• Anticipated Study Start Date: Oct 1, 2023
• Anticipated Primary Completion Date: Jan 10, 2025
• Anticipated Study Completion Date: Mar 31, 2025

Arms and Interventions

Arm	Intervention/Treatment
Experimental: BCI treatment Group using the IpsiHand Phase 1: Group 1 subjects will receive an IpsiHand Screening System to complete a remote EEG Screening. Subjects will undergo an EEG screening protocol to ensure that a consistent control signal will be present to control the IpsiHand device. After an EEG screening session is complete, the participants screening data will be analyzed to ensure that sufficient cortical signals are present. Randomization for assignment to group 1 or 2 will then occur. Once assigned to group 1, if consistent signals are found, the participant will then continue to Phase 2. Phase 2: Group 1 subjects will be provided with a Neurolutions IpsiHand BCI system, which combines a novel powered exoskeleton with a commercial EEG amplifier and active electrode system. The exoskeleton opens and closes the patient's hand in a three-finger pinch grip. Patients will use the BCI system on a minimum of 5 days per week for 12 weeks. Patients will complete five or more 10-minute runs of the BCI task per day.	Device: Neurolutions IpsiHand System; The IpsiHand system utilizes a Brain-Computer Interface (BCI) to enable operation of a robotic hand exoskeleton worn on the hand and wrist as participants are guided through a rehabilitation program on a tablet. Participants will complete 12 weeks of home therapy with the IpsiHand system. Motor function of their impaired upper extremity will be evaluated at baseline, at 4-week intervals, and 12 weeks completion of IpsiHand use.
Experimental: Standard of Care - Home Exercise Program for Upper Extremity Phase 1: Group 1 subjects will receive an IpsiHand Screening System to complete a remote EEG Screening. Once randomized, the participant will be assigned to group 2 to begin standard of care treatment at home. Phase 2: After being assigned to Group 2, subjects will serve as the control group in the study. Subjects will receive a customized home range of motion exercise program. Subjects will be recommended to complete their exercises daily, 5 out of 7 days per week for 12 weeks to control for the non-specific motor and sensory effects of BCI training. To help ensure compliance with the at-home portion of the protocol in the control group, participants will receive daily virtual monitoring from the study clinical specialist.	Other: Standard of Care - Home Exercise Program for Upper Extremity; Subjects will receive a customized home range of motion exercise program. Subjects will be recommended to complete their exercises daily, 5 out of 7 days per week for 12 weeks

Outcome Measures

Primary Outcome Measures

1. Upper Extremity Remote Fugl-Meyer [Baseline assessment]

   Valid assessment tool of upper extremity motor function in persons chronic stroke with moderate to severe deficits. Lowest score 0, highest score 66.

2. Upper Extremity Remote Fugl-Meyer [2 week assessment]

   Valid assessment tool of upper extremity motor function in persons chronic stroke with moderate to severe deficits. Lowest score 0, highest score 66.

3. Upper Extremity Remote Fugl-Meyer [4 week assessment]

   Valid assessment tool of upper extremity motor function in persons chronic stroke with moderate to severe deficits. Lowest score 0, highest score 66.

4. Upper Extremity Remote Fugl-Meyer [6 week assessment]

   Valid assessment tool of upper extremity motor function in persons chronic stroke with moderate to severe deficits. Lowest score 0, highest score 66.

5. Upper Extremity Remote Fugl-Meyer [8 week assessment]

   Valid assessment tool of upper extremity motor function in persons chronic stroke with moderate to severe deficits. Lowest score 0, highest score 66.

6. Upper Extremity Remote Fugl-Meyer [10 week assessment]

   Valid assessment tool of upper extremity motor function in persons chronic stroke with moderate to severe deficits. Lowest score 0, highest score 66.

7. Upper Extremity Remote Fugl-Meyer [12 week assessment (outcome assessment)]

   Valid assessment tool of upper extremity motor function in persons chronic stroke with moderate to severe deficits. Lowest score 0, highest score 66.

Secondary Outcome Measures

1. Motor Activity Log [Baseline assessment]

   Subjective assessment of use of hemiparetic arm in daily activity following stroke; lowest score=0, highest score= 140

2. Motor Activity Log [12 week completion]

   Subjective assessment of use of hemiparetic arm in daily activity following stroke; lowest score=0, highest score=140

3. Gross Grasp Strength [Baseline assessment]

   Evaluation of gross grasp strength via dynamometry; lowest score=0 lbs, maximal score 150lbs

4. Gross Grasp Strength [12 week completion]

   Evaluation of gross grasp strength via dynamometry; lowest score= 0lbs, highest score =150lbs

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 85 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

1. Adults age (18-85)

2. Adults who sustained a CVA

3. Have upper extremity hemiparesis/hemiplegia

4. Participants who are not receiving Botox Injections for the upper extremity may be included. Should a participant be receiving Botox injections for the upper extremity, they may be included but Botox administration must be timed to coincide within a week of the beginning of training.

Exclusion Criteria:

1. Participants who are not receiving Botox Injections for the upper extremity may be included. Should a participant be receiving Botox injections for the upper extremity, they may be included but Botox administration must be timed to coincide within a week of the beginning of training.

2. Participants who are too cognitively impaired to understand the task or provide informed consent will be excluded. A Short-Blessed Test score of 8 or more will be excluded.

3. Participants who have contractures in the affected wrist and digits will be excluded, as the device will not comfortably fit.

4. Participants who have receptive aphasia and unable to follow written directions will be excluded. A score of 6 or less on the MS Aphasia Screening Test will be excluded.

5. Participants receiving any formal upper extremity therapy will be excluded.

6. Participants with ataxia apraxia or severe psychiatric illness (other than post stroke depression) will be excluded.

7. Participants who are pregnant or breast-feeding will be excluded.

8. Participants who have nerve or sensory impairment that may limit or interfere with their ability to sense pain will be excluded.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Neurolutions	Saint Louis	Missouri	United States	63110

Sponsors and Collaborators

• Neurolutions, Inc.
• Washington University School of Medicine

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

• Theta-gamma coupling as a cortical biomarker of brain-computer interface-mediated motor recovery in chronic stroke
• A variables associated with occupational and physical therapy stroke rehabilitation utilization and outcomes
• Inequities in access to inpatient rehabilitation after stroke: an international scoping review
• Clinical practice. Rehabilitation after stroke
• Brain-Computer Interface in Stroke Rehabilitation
• Think to move: a neuromagnetic brain-computer interface (BCI) system for chronic stroke
• Feasibility of a new application of noninvasive Brain Computer Interface (BCI): a case study of training for recovery of volitional motor control after stroke
• Brain-computer interface-based robotic end effector system for wrist and hand rehabilitation: results of a three-armed randomized controlled trial for chronic stroke
• An evaluation framework for a rural home-based telerehabilitation network
• Disparities in postacute stroke rehabilitation disposition to acute inpatient rehabilitation vs. home: findings from the North Carolina Hospital Discharge Database
• Barriers to care among racial/ethnic groups under managed care
• Stroke patients' and carers' perception of barriers to accessing stroke information
• Rehabilitation with poststroke motor recovery: a review with a focus on neural plasticity
• Brain-computer interface with somatosensory feedback improves functional recovery from severe hemiplegia due to chronic stroke
• Efficacy of brain-computer interface-driven neuromuscular electrical stimulation for chronic paresis after stroke

Publications

None provided.

• Responsible Party: Neurolutions, Inc.
• ClinicalTrials.gov Identifier: NCT05965713
• Other Study ID Numbers: National Remote IpsiHand Study
• First Posted: Jul 28, 2023
• Last Update Posted: Jul 28, 2023
• Last Verified: Jul 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: Yes
• Product Manufactured in and Exported from the U.S.: No
• Keywords provided by Neurolutions, Inc.: Neurolutions; IpsiHand
• Additional relevant MeSH terms: Stroke; Paresis

Study Results

No Results Posted as of Jul 28, 2023