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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
The Catholic University of America
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Diagnosis of stroke more than six months prior to entry into the study
  2. Impaired ability to open affected the hand
  3. At least trace ability to extend the wrist and fingers

Exclusion Criteria:

  1. 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
  2. Have excessive pain in any joint of the affected extremity that could limit ability to cooperate with the protocols
  3. Have serious uncontrolled medical problems as judged by the project therapist
  4. Receiving oral or injected antispasticity medications during study treatment
  5. MCP and IP passive extension limit > 30 degrees from full extension
  6. 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

First Posted
August 21, 2017
Last Updated
August 26, 2020
Sponsor
The Catholic University of America
Collaborators
MedStar National Rehabilitation Network
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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
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Home Therapy for Stroke Rehabilitation Using the HandSOME Exoskeleton

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