- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02419222
Feasibility of Using Prism Adaptation to Treat Spatial Neglect and Motor Function in Stroke
August 16, 2017 updated by: Kessler Foundation
Feasibility of Using Prism Adaptation to Treat Spatial Neglect and Motor Function in Stroke Survivors With Multiple Lesions
This research project is a study designed to address both motor and cognitive changes after stroke.
Treatment for SN is elusive however there is support for prism adaptation treatment (PAT).
Therapists need to know more about the effects of this treatment and if it is feasible in a group of stroke survivors with multiple lesions because these are the patients they are treating in the clinical setting.
Also, it has not been investigated that using PAT to remediate SN will then as a result increase spontaneous UE movement of the weak limb.
Study Overview
Detailed Description
This research project is a study designed to address both motor and cognitive changes after stroke, two common stroke disabilities.
For example: two third of patients reported loss of upper limb function as a major problem after stroke and spatial neglect occurs in more than 350,000 US right hemisphere stroke survivors annually.
These two impairments if not treated, lead to immediate impairment in basic life activities, long term functional disability, increased risk for falls and increased healthcare costs.
The literature displays many strong research studies that trialed the use of multiple treatment approaches to remediate spatial neglect, including prism adaptation treatment (PAT), resulting in positive results.
Similar findings result for treatment studies that attempt to remediate the upper extremity (UE).
However, in all group of patients that were tested in these studies (both for spatial neglect and UE dysfunction) only had one stroke and past medical histories that were unremarkable.
Rehabilitation professionals help clients that have had all types of strokes achieve improved quality of life by helping to increase independence by remediating impairment.
In addition, these professionals need to know more about the effects of PAT in stroke survivors with multiple lesions because these are patients commonly being treated in the clinical setting.
Also, it has not been investigated whether using PAT, a very promising and easy to administer treatment, to remediate spatial neglect will also increase spontaneous UE movement of the limb affected by the stroke because of an influence on motor-intentional aiming errors.
Thus, in this pilot research proposal, the researcher intends to first investigate the feasibility of this two week treatment on stroke survivors that have had multiple lesions and second verify if PAT will improve spatial neglect and jointly increase spontaneous movement of the UE.
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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New Jersey
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Saddle Brook, New Jersey, United States, 07663
- Kessler Insitute for Rehabilitaiton
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West Orange, New Jersey, United States, 07052
- Kessler Institute for Rehabiltiation
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Between the ages of 18 and 90.
- New stroke on the right side of the brain.
- Has an UE impairment of the arm affected by the stroke (WMFT score of less than 75).
- Has the presence of spatial neglect (greater than 1 on the KF-NAP).
- Is able to give informed consent.
- Past medical history includes having had a stroke or more than one. This can be ischemic or hemorrhagic, and on either side of the brain.
Exclusion Criteria:
- Is under the age of 18.
- Has severe communication deficit.
- Has a left brain stroke as the primary diagnosis and/or the primary diagnosis is anything other than stroke.
- Is blind in one or both eyes.
- Is not staying at the inpatient rehabilitation hospital
- Has a cognitive impairment that inhibits their ability to recall information.
- Has severely impaired upper extremity function in bilateral arms (cannot participate in the prism task).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Prism Adaptation
Prism Adaptation Treatment is 20 minutes long, administered 10 consecutive days
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PAT uses wedged prism lenses to displace the entire visual field horizontally to the left or right (depending on the orientation of the base of the prism).
The left-base prism lenses (thicker on the left) shift the entire visual field to the right.
The result is a curving reaching trajectory, aiming toward the image location (right to the actual location) and then corrected toward the actual location.
After several reaching movement, the coordinates of motor and visual systems are aligned, which in other words, is that the motor output adapts to the visual input, and thus the reaching trajectory is straight ahead to the object.
This visually-guided goal-oriented movement is essential in PAT.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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CBS via Kessler Foundation Neglect Assessment Process
Time Frame: 30 minutes
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The CBS is a 10-item scale for evaluating the severity of spatial neglect (Azouviet al., 1996).
Thus, the CBS captures the heterogeneity of spatial neglect in the most functional way.
The items include limb awareness, personal belongings, dressing, grooming, gaze orientation, auditory attention, navigation, collisions, eating, cleaning after a meal.
Each item is scored from 0-3.
Based on a CBS total score (range 0-30), a stroke survivor with unilateral brain damage can be categorized as no neglect (CBS=0), mild (CBS= 1-10), moderate (CBS= 11-20), or severe (CBS= 20-30).
In 2012, Chen et al. addressed this obstacle by standardizing the method to use the CBS reliably in the clinic and trademarked the process to use in conjunction with the CBS as the Kessler Foundation Neglect Assessment Process (CBS via KF-NAP™).
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30 minutes
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Behavior Inattention Test
Time Frame: 15 minutes
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The Behavior Inattention Test is a validated, widely used battery for the assessment of neglect.
It has multiple subtests in the conventional battery, for example line crossing and letter cancelation tests .
The conventional test battery will be used; the total score is out of 146 with a cut off score of 128 for spatial neglect (Wilson, et al. 1987).
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15 minutes
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Motor Activity Log
Time Frame: 15 minutes
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The Motor Activity Log, a structured interview, will be used to assess how the patient feels they use their arm during specific activities (Uswatte, Taub, Morris, Vignolo, McCulloch, 2005).
This will be the outcome measure used to determine spontaneous movement.
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15 minutes
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Functional Independence Measure
Time Frame: 30 minutes
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Functional Independence Measure (FIM) is a reliable and valid assessment of function and the gold standard in rehabilitation facilities.
It consists of 18 items assessing the level of independence in two domains; motor and cognitive.
Each item is scored from 1 (maximal) to 7 (independent) (Ottenbacher, et al 1996).
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30 minutes
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Wolf Motor Function Test
Time Frame: 45 min
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The WMFT is a quantitative measure of upper extremity motor ability through timed and functional tasks (Wolf et al., 1989).
There are 21 items with 3 parts (time, functional ability and strength).
The person's less affected arm is examined followed by the most affected side.
The maximum score is a 75.
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45 min
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Kimberly P Hreha, MS, Kessler Foundation
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2015
Primary Completion (Actual)
December 1, 2016
Study Completion (Actual)
December 1, 2016
Study Registration Dates
First Submitted
April 14, 2015
First Submitted That Met QC Criteria
April 16, 2015
First Posted (Estimate)
April 17, 2015
Study Record Updates
Last Update Posted (Actual)
August 21, 2017
Last Update Submitted That Met QC Criteria
August 16, 2017
Last Verified
August 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R-853-14
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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