Home Therapy for Stroke Rehabilitation Using the HandSOME Exoskeleton (HandSOME)
Primary Purpose
Stroke
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
HandSOME
Sponsored by

About this trial
This is an interventional treatment trial for Stroke
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of stroke more than six months prior to entry into the study
- Impaired ability to open affected the hand
- At least trace ability to extend the wrist and fingers
Exclusion Criteria:
- Have cognitive deficits that could negatively affect their ability to complete the protocols as evidenced by a score of 24 or less on the Folstein Mini-Mental State Examination
- Have excessive pain in any joint of the affected extremity that could limit ability to cooperate with the protocols
- Have serious uncontrolled medical problems as judged by the project therapist
- Receiving oral or injected antispasticity medications during study treatment
- MCP and IP passive extension limit > 30 degrees from full extension
- Excessive tone in the fingers and thumb as determined by Ashworth scores >=3
Sites / Locations
- MedStar National Rehabilitation Network
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
HandSOME
Arm Description
The intervention is given to this group.
Outcomes
Primary Outcome Measures
Change in Fugl-Meyer Test of Arm Function
clinical test of arm motor ability and impairment
Change in Action Research Arm Test
clinical test of the functional limitations of the upper extremities
Change in Motor Activity Log
assess the amount and quality of limb use at home
Secondary Outcome Measures
Change in Fugl-Meyer Test of Arm Function at followup
clinical test of arm motor ability and impairment
Change in Action Research Arm Test at followup
clinical test of the functional limitations of the upper extremities
Change in Motor Activity Log at followup
assess the amount and quality of limb use at home
Full Information
NCT ID
NCT03263286
First Posted
August 21, 2017
Last Updated
August 26, 2020
Sponsor
The Catholic University of America
Collaborators
MedStar National Rehabilitation Network
1. Study Identification
Unique Protocol Identification Number
NCT03263286
Brief Title
Home Therapy for Stroke Rehabilitation Using the HandSOME Exoskeleton
Acronym
HandSOME
Official Title
Home Therapy for Upper Limb Stroke Rehabilitation Using the HandSOME Exoskeleton
Study Type
Interventional
2. Study Status
Record Verification Date
August 2020
Overall Recruitment Status
Completed
Study Start Date
April 15, 2017 (Actual)
Primary Completion Date
October 7, 2019 (Actual)
Study Completion Date
October 7, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Catholic University of America
Collaborators
MedStar National Rehabilitation Network
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
This research will evaluate the potential for a novel hand orthosis (HandSOME) to help stroke victims regain functional use of their hand and regain independent living. Participants will use the HandSOME at home regularly for 8 weeks. Clinical evaluations will measure changes from the intervention after the 8 weeks and also at a 3 month followup.
Detailed Description
After stroke, individuals often have great difficulty with using the affected hand in functional tasks. The hand frequently suffers from finger flexor hypertonia as well as finger extensor weakness. This leads to increased difficulty in grasp and release of objects. HandSOME is a light weight wearable hand orthosis that increases range of motion and decreases effort during grasping tasks. The goal of this study is to evaluate the HandSOME device's effectiveness in the rehabilitation of stroke patients through an 8 week intervention. Eligible subjects will use the device daily at home for 8 weeks with one visit per week to the clinic to evaluate progress and troubleshoot problems with the device. The hypotheses are that the gains from the 8 weeks of training will be statistically significant and clinically important (defined as gains of greater than 10% of full scale) in the domains of impairment, function and amount of arm use.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Actual)
8. Arms, Groups, and Interventions
Arm Title
HandSOME
Arm Type
Experimental
Arm Description
The intervention is given to this group.
Intervention Type
Device
Intervention Name(s)
HandSOME
Intervention Description
Participants use the HandSOME orthosis daily for 8 weeks.
Primary Outcome Measure Information:
Title
Change in Fugl-Meyer Test of Arm Function
Description
clinical test of arm motor ability and impairment
Time Frame
Change from baseline Fugl-Meyer score at 2 months
Title
Change in Action Research Arm Test
Description
clinical test of the functional limitations of the upper extremities
Time Frame
Change from baseline Action Research Arm Test score at 2 months
Title
Change in Motor Activity Log
Description
assess the amount and quality of limb use at home
Time Frame
Change from baseline Motor Activity Log score at 2 months
Secondary Outcome Measure Information:
Title
Change in Fugl-Meyer Test of Arm Function at followup
Description
clinical test of arm motor ability and impairment
Time Frame
Change from baseline Fugl-Meyer score at 5 months
Title
Change in Action Research Arm Test at followup
Description
clinical test of the functional limitations of the upper extremities
Time Frame
Change from baseline Action Research Arm Test score at 5 months
Title
Change in Motor Activity Log at followup
Description
assess the amount and quality of limb use at home
Time Frame
Change from baseline Motor Activity Log score at 5 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of stroke more than six months prior to entry into the study
Impaired ability to open affected the hand
At least trace ability to extend the wrist and fingers
Exclusion Criteria:
Have cognitive deficits that could negatively affect their ability to complete the protocols as evidenced by a score of 24 or less on the Folstein Mini-Mental State Examination
Have excessive pain in any joint of the affected extremity that could limit ability to cooperate with the protocols
Have serious uncontrolled medical problems as judged by the project therapist
Receiving oral or injected antispasticity medications during study treatment
MCP and IP passive extension limit > 30 degrees from full extension
Excessive tone in the fingers and thumb as determined by Ashworth scores >=3
Facility Information:
Facility Name
MedStar National Rehabilitation Network
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20010
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
28324934
Citation
Tianyao Chen, Lum PS. Hand rehabilitation after stroke using a wearable, high DOF, spring powered exoskeleton. Annu Int Conf IEEE Eng Med Biol Soc. 2016 Aug;2016:578-581. doi: 10.1109/EMBC.2016.7590768.
Results Reference
background
Learn more about this trial
Home Therapy for Stroke Rehabilitation Using the HandSOME Exoskeleton
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