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Bilateral Versus Unilateral Task Retraining Using the SaeboFlex Orthosis

Primary Purpose

Muscle Spasticity

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Task Training
Sponsored by
University of Missouri-Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Muscle Spasticity

Eligibility Criteria

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

Inclusion Criteria:

  • at least 18 years of age
  • >6 months post stroke
  • diagnosis of first stroke
  • medically stable
  • ability to follow multipart verbal directions
  • score of >26 on Mini-Mental Status Exam
  • achieve 10 degrees elbow flexion
  • 1/4 range volitional finger flexion when hand positioned in wrist and finger extension
  • capable of standing for >2 minutes without an assistive ambulatory device
  • maintain independence in self-care or have a caretaker to provide assistance
  • no concurrent skilled therapy treatment
  • not participating in any experimental rehabilitation or drug studies.

Exclusion Criteria:

  • more than one stroke/multiple strokes
  • receptive aphasia
  • medically documented dementia
  • score less than 26 on Mini Mental Status Exam
  • contractures or joint deformities in the affected hand or wrist that impede the ability to use the device
  • inability to transfer 12 balls crate right and 12 balls crate left, while using the Saeboflex device on the affected arm, by the end of a 5-day training session.

Sites / Locations

  • University of Missouri, Lewis and Clark Hall

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

1 Unilateral Group

2 Bilateral training

Arm Description

This group will wear the SaeboFlex orthosis on their affected extremity and do exercises with that extremity only. SaeboFlex exercises include moving the ball in high repetition of grasp and release while wearing the SaeboFlex orthosis to various positions individualized to each participant based on movement deficits, as well as Task Training (using the affected arm during specific functional activities to use newly acquired movement patterns)

Members of this group will wear the SaeboFlex orthosis on the affected extremity and do exercises with the affected extremity and the non-affected extremity at the same time. SaeboFlex exercises include moving the ball in high repetition of grasp and release while wearing the SaeboFlex orthosis to various positions individualized to each participant based on movement deficits, as well as Task Training (using the affected arm during specific functional activities to use newly acquired movement patterns)

Outcomes

Primary Outcome Measures

Wolf Motor Function Test (WMFT)

Secondary Outcome Measures

Canadian Occupational Performance Measure

Full Information

First Posted
May 4, 2009
Last Updated
October 24, 2017
Sponsor
University of Missouri-Columbia
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1. Study Identification

Unique Protocol Identification Number
NCT00893776
Brief Title
Bilateral Versus Unilateral Task Retraining Using the SaeboFlex Orthosis
Official Title
The Effectiveness of Bilateral Versus Unilateral Task Retraining Using the SaeboFlex Orthosis in Individuals With Subacute and Chronic Stroke.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2017
Overall Recruitment Status
Terminated
Why Stopped
Insufficient time for study extenuating personal circumstances of PI
Study Start Date
June 2009 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
December 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Missouri-Columbia

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
A small, pilot study consisting of twelve participants with subacute (6-12 months post-stroke)and chronic stroke (1year+ post-stroke)living in and around Columbia area. The twelve participants will randomly be selected to participate in either unilateral (one-handed) task training (6 participants) or bilateral (two-handed) task training (6 participants) with the SaeboFlex orthosis. Each group will undergo six assessments to establish pre-testing baseline and qualification, followed by a training session, four-week combined home and clinic program, and post-testing to determine changes in affected arm use and function. The hypothesis is that two-handed training will before effective than one-handed training.
Detailed Description
The SaeboFlex device is a mechanical orthosis that promotes grasp and release and functional movement of an upper limb that has impaired movement due to a stroke. Many researchers have found that incorporating both the affected and unaffected limb together during exercises (bilateral task training) results in increased functional use of the affected limb as compared to only performing exercises with the affected limb. Therefore, we want to determine if bilateral task training is more effective than unilateral task training with the use of the SaeboFlex device in subacute and chronic stroke rehabilitation. For the unilateral training group, exercises will be completed with only the affected hand using the Saebo device. For the bilateral group, the Saebo will be on the affected hand, no device on the unaffected hand, and both arms will do the exact same movements/exercises at the same time. The participants will be videotaped and photographed moving balls without the device, with the device at the start of the study, with the device midway through the study, and at the end of the study. This will be done for the purpose of providing participant feedback regarding their progress and for report of outcomes upon completion of the project. Faces will be omitted from all photographic media at the request of the participant, and the participant may decline photographic media at any time without having to withdraw from the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Muscle Spasticity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
9 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1 Unilateral Group
Arm Type
Active Comparator
Arm Description
This group will wear the SaeboFlex orthosis on their affected extremity and do exercises with that extremity only. SaeboFlex exercises include moving the ball in high repetition of grasp and release while wearing the SaeboFlex orthosis to various positions individualized to each participant based on movement deficits, as well as Task Training (using the affected arm during specific functional activities to use newly acquired movement patterns)
Arm Title
2 Bilateral training
Arm Type
Experimental
Arm Description
Members of this group will wear the SaeboFlex orthosis on the affected extremity and do exercises with the affected extremity and the non-affected extremity at the same time. SaeboFlex exercises include moving the ball in high repetition of grasp and release while wearing the SaeboFlex orthosis to various positions individualized to each participant based on movement deficits, as well as Task Training (using the affected arm during specific functional activities to use newly acquired movement patterns)
Intervention Type
Other
Intervention Name(s)
Task Training
Intervention Description
Task training is the movement of balls in an individually prescribed fashion using the SaeboFlex orthosis on the affected extremity.
Primary Outcome Measure Information:
Title
Wolf Motor Function Test (WMFT)
Time Frame
Before and immediately after intervention
Secondary Outcome Measure Information:
Title
Canadian Occupational Performance Measure
Time Frame
Before and immediately after intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: at least 18 years of age >6 months post stroke diagnosis of first stroke medically stable ability to follow multipart verbal directions score of >26 on Mini-Mental Status Exam achieve 10 degrees elbow flexion 1/4 range volitional finger flexion when hand positioned in wrist and finger extension capable of standing for >2 minutes without an assistive ambulatory device maintain independence in self-care or have a caretaker to provide assistance no concurrent skilled therapy treatment not participating in any experimental rehabilitation or drug studies. Exclusion Criteria: more than one stroke/multiple strokes receptive aphasia medically documented dementia score less than 26 on Mini Mental Status Exam contractures or joint deformities in the affected hand or wrist that impede the ability to use the device inability to transfer 12 balls crate right and 12 balls crate left, while using the Saeboflex device on the affected arm, by the end of a 5-day training session.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Giulianne Krug, MA, OTR/L
Organizational Affiliation
University of Missouri, Occupational Therapy and Occupational Science
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Missouri, Lewis and Clark Hall
City
Columbia
State/Province
Missouri
ZIP/Postal Code
65211
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Links:
URL
http://www.saebo.com
Description
This is the device we are using for the study.

Learn more about this trial

Bilateral Versus Unilateral Task Retraining Using the SaeboFlex Orthosis

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