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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00989430
Other study ID # AMBarrett3
Secondary ID Spatial Neglect
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date October 2012
Est. completion date October 2021

Study information

Verified date February 2021
Source Kessler Foundation
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this research study with a randomized controlled design is to examine the effects of prism adaptation treatment on two visual-spatial recovery components. After a stroke, an "internal GPS", locating where objects or people lie in a particular area of space, may be impaired. Alternately, a stroke may impair precise visual-spatial hand and body aiming movements. The research team wishes to discover whether prism adaptation treatment (two weeks of daily 20-min sessions of goal-directed movement with prism goggles) affects visual-spatial where or aiming errors selectively after stroke. This research represents one of the first attempts to apply what we know about the brain from neuroscience research, to modern clinical rehabilitation practices.


Description:

The purpose of this research study with a randomized controlled design is to examine the effects of prism adaptation treatment on two visual-spatial recovery components. After a stroke, an "internal GPS", locating where objects or people lie in a particular area of space, may be impaired. Alternately, a stroke may impair precise visual-spatial hand and body aiming movements. The research team wishes to discover whether prism adaptation treatment (two weeks of daily 20-min sessions of goal-directed movement with prism goggles) affects visual-spatial where or aiming errors selectively after stroke. This research represents one of the first attempts to apply what we know about the brain from neuroscience research, to modern clinical rehabilitation practices.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 160
Est. completion date October 2021
Est. primary completion date October 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - The subject is 18 to 100 years of age, inclusive. - The subject has had a stroke on the right side of the brain. - The subject is able to give Informed consent. - The subject has a spatial neglect (if known). - The subject is able and willing to comply with the study protocol, including availability for all scheduled clinic visits. Exclusion Criteria: - The subject has or had a serious brain condition other than stroke.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Prism Adaptation Treatment
Wearing prism goggles and performing visuomotor tasks during therapy sessions.

Locations

Country Name City State
United States Kessler Institute for Rehabilitation West Orange New Jersey

Sponsors (2)

Lead Sponsor Collaborator
Kessler Foundation U.S. Department of Education

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Kessler Foundation Neglect Assessment Process a performance based and behavioral measure for spatial neglect that utilizes and standardizes the administration of the Catherine Bergego Scale (CBS) 6 months
Secondary Behavior Inattention Test Conventional subtest, a set of paper and pencil test for spatial neglect 2 weeks
Secondary Barthel Index A functional independence assessment of daily tasks 2 weeks
See also
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Recruiting NCT04227132 - Evaluation of an Adaptive Computerized Training for Rehabilitation of Spatial Neglect in Stroke Survivors N/A