Skip to main content
OpenTrials
Completed

NCT Number: NCT02935270

Examining Measurement of Behavioral Neglect Post Stroke

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Medical University of South Carolina

Charleston, South Carolina, 29425, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Unilateral hemispheric stroke
  • 18 years or older

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

Treatment and study plan

Primary outcomes

  1. Catherine Bergego Scale

    Time frame: One-time assessment scheduled over 1-2 days

  2. Behavioral Inattention Test

    Time frame: One-time assessment scheduled over 1-2 days

  3. Naturalistic Action Test

    Time frame: One-time assessment scheduled over 1-2 days

  4. Virtual Reality Lateralized Attention Test

    Time frame: One-time assessment scheduled over 1-2 days

  5. Kinematic Assessment of Arm Movement

    Time frame: One-time assessment scheduled over 1-2 days

Secondary outcomes

  1. Arm Use measured by Accelerometers

    Time frame: One-time assessment scheduled over 3 days

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

Sponsors and collaborators

Lead sponsor

Medical University of South Carolina

Other

Registry information

Important dates

Study start
2016
Primary completion
2020
Study completion
2020
First posted
Oct 17, 2016
Registry last updated
Nov 25, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.