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Examining Measurement of Behavioral Neglect Post Stroke

Completed
Conditions
Hemispatial Neglect
Stroke
Registration Number
NCT02935270
Lead Sponsor
Medical University of South Carolina
Brief Summary

The purpose of this study is to examine measurement of unilateral neglect post stroke. Although a number of clinical assessments are used to measure neglect, it is unclear whether items from some of the most commonly used assessments are able to effectively and comprehensively measure neglect. This study will determine whether these assessments measure different aspects of neglect and whether items from various neglect assessments can be combined to more effectively measure neglect.

Detailed Description

Many individuals have difficulty attending to the affected side of their body or to the affected side of space after stroke (unilateral neglect). Although a number of clinical assessments are used to measure this inattention, it is unclear whether items from some of the most commonly used assessments are able to effectively and comprehensively measure inattention. Clinical assessments provide critical information to clinicians and researchers and are used to inform treatment and document patient progress. Therefore, it is important that investigators more closely examine these existing assessments.

Individuals who demonstrate impaired attention to the affected side after stroke also have greater motor impairment than individuals who do not have impaired attention, but investigators do not know how inattention affects reaching movements using the impaired arm. This study will examine various methods used to assess inattention to the affected side after stroke and also examine how inattention affects reaching movements of the impaired arm.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
55
Inclusion Criteria
  • Unilateral hemispheric stroke
  • 18 years or older
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Exclusion Criteria
  • Severe aphasia
  • Inability to follow 2-step directions
  • Presence of other neurological disease that may impair vision or perception during performance of evaluation procedures
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Naturalistic Action TestOne-time assessment scheduled over 1-2 days
Catherine Bergego ScaleOne-time assessment scheduled over 1-2 days
Behavioral Inattention TestOne-time assessment scheduled over 1-2 days
Virtual Reality Lateralized Attention TestOne-time assessment scheduled over 1-2 days
Kinematic Assessment of Arm MovementOne-time assessment scheduled over 1-2 days
Secondary Outcome Measures
NameTimeMethod
Arm Use measured by AccelerometersOne-time assessment scheduled over 3 days

Accelerometers will be issued on the first assessment day. Participants will wear accelerometers for 3 days.

Trial Locations

Locations (1)

Medical University of South Carolina

🇺🇸

Charleston, South Carolina, United States

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