- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07538076
Validation of Web-Based Star Cancellation and Line Bisection Tests in Hemiplegic Stroke
Development and Validity of Web Based Star Cancellation Test and Line Bisection Test in the Assessment of Visuospatial Neglect in Hemiplegic Stroke Patients
The goal of this observational study is to evaluate the clinical usability and diagnostic performance of newly developed web-based Star Cancellation and Line Bisection tests in assessing visuospatial neglect in hemiplegic stroke patients. It will also compare these digital tests with conventional paper-and-pencil assessments.
The main questions it aims to answer are:
Can the web-based Star Cancellation and Line Bisection tests accurately distinguish between stroke patients with and without visuospatial neglect? Do digital test parameters (such as completion time, search speed, and search patterns) provide additional clinical information beyond conventional test scores? Researchers will compare the results of the web-based tests with standard paper-and-pencil tests to evaluate their diagnostic accuracy and clinical validity.
Participants will:
Complete conventional paper-and-pencil Star Cancellation and Line Bisection tests Perform web-based (digital) versions of the same tests using a tablet and stylus Undergo routine clinical and cognitive assessments as part of standard care Provide demographic and clinical information
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study is designed as a cross-sectional, comparative, diagnostic accuracy and methodological validation study to evaluate newly developed web-based (browser-based) Star Cancellation Test (SCT) and Line Bisection Test (LBT) for the assessment of visuospatial neglect in hemiplegic stroke patients.
Visuospatial neglect is a common neuropsychological condition following stroke, particularly after right hemisphere lesions, and is associated with significant functional impairment. In clinical practice, neglect is typically assessed using paper-and-pencil tests such as cancellation tasks and line bisection tests. While these methods are widely used, they rely on manual scoring and provide limited information about the underlying search process and performance dynamics.
The digital tests developed in this study are designed to preserve the core structure and spatial characteristics of conventional assessments while enabling automated scoring and recording of additional performance metrics. These include process-based parameters such as completion time, search speed, search path characteristics, and ineffective or off-target responses. The system operates on a web-based platform without requiring software installation and is accessible through standard consumer devices, aiming to improve standardization, accessibility, and scalability in clinical settings.
Participants will be recruited from patients admitted to a physical medicine and rehabilitation clinic and will be classified into three groups based on independent clinical assessment: (1) stroke patients with visuospatial neglect, (2) stroke patients without visuospatial neglect, and (3) age- and sex-matched healthy controls without neurological disease. The presence of visuospatial neglect will be determined using routine clinical reference standards, including established paper-and-pencil neuropsychological tests and behavioral assessment scales. Digital test results will not be used in diagnostic classification to avoid incorporation bias.
All participants will complete both conventional paper-and-pencil and web-based versions of the Star Cancellation Test and Line Bisection Test under standardized conditions in a quiet clinical environment. To minimize potential order effects such as fatigue or learning, the sequence of test administration will be counterbalanced across participants. Digital assessments will be performed using a tablet device and stylus pen to ensure consistency in motor and spatial interaction.
The primary objective of the study is to evaluate the diagnostic performance of the digital tests in distinguishing between patients with and without visuospatial neglect. Secondary objectives include examining the additional clinical value of process-based digital metrics and assessing the agreement between conventional and digital test outcomes.
Statistical analyses will be conducted to assess diagnostic accuracy using receiver operating characteristic (ROC) curve analysis, including estimation of area under the curve (AUC), sensitivity, and specificity. Multivariate modeling approaches may be applied to explore the contribution of multiple digital parameters to diagnostic classification. Descriptive and correlational analyses will be used to evaluate relationships between digital performance measures and clinical variables.
Data will be collected and stored in a secure and anonymized format. Automated data capture within the digital platform will reduce manual entry errors and improve data completeness. All analyses will be performed using standard statistical software.
This study aims to provide a clinically applicable, accessible, and standardized digital alternative to conventional visuospatial neglect assessment methods, while also contributing novel process-based performance measures to the field.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Melisa Zengin, MD
- Phone Number: +905414005688
- Email: melisazngn@gmail.com
Study Locations
-
-
Kadikoy
-
Istanbul, Kadikoy, Turkey (Türkiye), 34722
- Istanbul Medeniyet University Goztepe Prof Dr Suleyman Yalcin City Hospital
-
Contact:
- Melisa Zengin, MD
- Phone Number: +905414005688
- Email: melisazngn@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age 18 to 80 years
- First-ever ischemic or hemorrhagic stroke
- Hemiplegia secondary to stroke
- Stroke in the subacute or chronic phase, defined as 1 to 24 months after stroke onset
- Ability to provide written informed consent
Exclusion Criteria:
- History of neurological or severe psychiatric disease before stroke that could significantly affect cognitive function or attention, such as brain tumor, traumatic brain injury, vasculitis, multiple sclerosis, or schizophrenia
- Severe visual field defect not attributable to visuospatial neglect, such as isolated homonymous hemianopia
- Severe upper extremity motor impairment or apraxia preventing interaction with the tablet or stylus pen
- Inability to understand test instructions, cooperate with the assessment, or complete the evaluation process
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Stroke patients with visuospatial neglect
The diagnosis of visuospatial neglect will be established using standard paper-and-pencil neuropsychological assessments routinely applied in clinical practice, including the Star Cancellation Test, Line Cancellation Test, Line Bisection Test, Letter Cancellation Test, figure copying tasks, and clock drawing test, along with the Catherine Bergego Scale. To classify a participant as having visuospatial neglect, pathological findings must be present in at least two of these assessments, with at least one being a performance-based paper-and-pencil test. These assessments are part of routine clinical evaluation in stroke patients.Digital test results will not be used for diagnostic classification. |
The intervention consists of a web-based Star Cancellation Test developed by the study investigators for the assessment of visuospatial neglect. This test is implemented as a browser-based application that can be accessed on standard devices without requiring software installation and is administered using a tablet and stylus pen to ensure consistent interaction. The digital Star Cancellation Test is based on the conventional paper-and-pencil version and includes both target and distractor stimuli. In addition to standard scoring, it automatically records performance measures such as the number of omitted targets, laterality index, completion time, search speed, and search path characteristics.
Other Names:
The intervention consists of a web-based Line Bisection Test developed by the study investigators for the assessment of visuospatial neglect. This test is implemented as a browser-based application that can be accessed on standard devices without requiring software installation and is administered using a tablet and stylus pen to ensure consistent interaction. The digital Line Bisection Test follows the conventional paradigm in which participants are asked to mark the midpoint of horizontal lines. In the digital version, line positions vary across trials, and deviation from the true midpoint is calculated automatically, along with measures of variability.
Other Names:
|
|
Stroke patients without visuospatial neglect
|
The intervention consists of a web-based Star Cancellation Test developed by the study investigators for the assessment of visuospatial neglect. This test is implemented as a browser-based application that can be accessed on standard devices without requiring software installation and is administered using a tablet and stylus pen to ensure consistent interaction. The digital Star Cancellation Test is based on the conventional paper-and-pencil version and includes both target and distractor stimuli. In addition to standard scoring, it automatically records performance measures such as the number of omitted targets, laterality index, completion time, search speed, and search path characteristics.
Other Names:
The intervention consists of a web-based Line Bisection Test developed by the study investigators for the assessment of visuospatial neglect. This test is implemented as a browser-based application that can be accessed on standard devices without requiring software installation and is administered using a tablet and stylus pen to ensure consistent interaction. The digital Line Bisection Test follows the conventional paradigm in which participants are asked to mark the midpoint of horizontal lines. In the digital version, line positions vary across trials, and deviation from the true midpoint is calculated automatically, along with measures of variability.
Other Names:
|
|
Control Group
Age- and sex-matched healthy control individuals without a history of neurological disease
|
The intervention consists of a web-based Star Cancellation Test developed by the study investigators for the assessment of visuospatial neglect. This test is implemented as a browser-based application that can be accessed on standard devices without requiring software installation and is administered using a tablet and stylus pen to ensure consistent interaction. The digital Star Cancellation Test is based on the conventional paper-and-pencil version and includes both target and distractor stimuli. In addition to standard scoring, it automatically records performance measures such as the number of omitted targets, laterality index, completion time, search speed, and search path characteristics.
Other Names:
The intervention consists of a web-based Line Bisection Test developed by the study investigators for the assessment of visuospatial neglect. This test is implemented as a browser-based application that can be accessed on standard devices without requiring software installation and is administered using a tablet and stylus pen to ensure consistent interaction. The digital Line Bisection Test follows the conventional paradigm in which participants are asked to mark the midpoint of horizontal lines. In the digital version, line positions vary across trials, and deviation from the true midpoint is calculated automatically, along with measures of variability.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Laterality Index of the Digital Star Cancellation Test
Time Frame: Baseline (single assessment during study visit)
|
The laterality index is calculated as the proportion of targets identified on the left side relative to the total number of identified targets.
It is used to assess spatial bias and distinguish between participants with and without visuospatial neglect.
|
Baseline (single assessment during study visit)
|
|
Mean Deviation in the Digital Line Bisection Test
Time Frame: Baseline (single assessment during study visit)
|
Mean deviation represents the average distance between the participant's marked midpoint and the true midpoint of horizontal lines.
It is used as a quantitative measure of spatial bias.
|
Baseline (single assessment during study visit)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Omitted Targets in the Digital Star Cancellation Test
Time Frame: Baseline (single assessment during study visit)
|
The total number of target stars not identified during the digital Star Cancellation Test.
This measure reflects incomplete visual exploration.
|
Baseline (single assessment during study visit)
|
|
Completion Time of the Digital Star Cancellation Test
Time Frame: Baseline (single assessment during study visit)
|
The total time required to complete the digital Star Cancellation Test, recorded automatically by the system.
|
Baseline (single assessment during study visit)
|
|
Search Speed in the Digital Star Cancellation Test
Time Frame: Baseline (single assessment during study visit)
|
The rate of target identification during the digital Star Cancellation Test, used to characterize visual search efficiency.
|
Baseline (single assessment during study visit)
|
|
Ineffective or Off-Target Responses in the Digital Star Cancellation Test
Time Frame: Baseline (single assessment during study visit)
|
The number of ineffective or off-target marking attempts recorded during the digital Star Cancellation Test.
|
Baseline (single assessment during study visit)
|
|
Variability of Performance in the Digital Line Bisection Test
Time Frame: Baseline (single assessment during study visit)
|
The standard deviation of deviations from the true midpoint across lines in the digital Line Bisection Test, used to assess response variability.
|
Baseline (single assessment during study visit)
|
|
Time Spent on Each Side of the Screen in the Digital Star Cancellation Test
Time Frame: Baseline (single assessment during study visit)
|
The amount of time spent exploring the left and right halves of the screen during the digital Star Cancellation Test, recorded automatically by the system.
This measure is used to assess lateralized visual exploration patterns.
|
Baseline (single assessment during study visit)
|
|
Search Path Characteristics in the Digital Star Cancellation Test
Time Frame: Baseline (single assessment during study visit)
|
Process-based measures describing the pattern of visual search during the digital Star Cancellation Test.
|
Baseline (single assessment during study visit)
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Participant-Reported Feasibility of the Digital Tests
Time Frame: Baseline (single assessment immediately after test completion)
|
Feasibility and user experience of the web-based Star Cancellation and Line Bisection tests, assessed using a brief investigator-developed questionnaire administered after completion of the digital assessments.
|
Baseline (single assessment immediately after test completion)
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Neglect Tests
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Stroke
-
National Assembly ClinicBayero University Kano, NigeriaRecruitingStroke | Stroke Hemorrhagic | Stroke Ischemic | Hemiparesis After StrokeNigeria
-
University of PittsburghRecruitingHemorrhagic Stroke | Embolic Stroke of Undetermined Source | Ischemic Stroke, Cryptogenic | Recurrent Ischemic Stroke | Ischemic Stroke, EmbolicUnited States
-
Mahidol UniversityNot yet recruitingIschemic Stroke | Hemorrhagic Stroke | Subacute Stroke | Chronic Stroke SurvivorsThailand
-
Mahidol UniversityRecruitingIschemic Stroke | Hemorrhagic Stroke | Subacute Stroke | Chronic Stroke PatientThailand
-
University Hospital, GhentRecruitingStroke | Stroke, Ischemic | Stroke, Acute | Stroke Sequelae | Stroke HemorrhagicBelgium
-
Moleac Pte Ltd.Not yet recruitingStroke | Stroke, Ischemic | Stroke Sequelae | Stroke, Cardiovascular | Strokes Thrombotic | Stroke, Embolic | Stroke, Cryptogenic
-
University of Illinois at ChicagoRecruitingStroke, Ischemic | Stroke Hemorrhagic | Stroke, CerebrovascularUnited States
-
IRCCS San Camillo, Venezia, ItalyRecruitingStroke | Stroke, Ischemic | Stroke Sequelae | Stroke HemorrhagicItaly
-
Samsung Medical CenterCompletedChronic Stroke | Subacute Stroke | ExoskeletonSouth Korea
-
Fondazione Don Carlo Gnocchi OnlusScuola Superiore Sant'Anna di Pisa; Fondazione Policlinico Universitario Campus...Not yet recruitingStroke | Stroke Hemorrhagic | Upper Limb Rehabilitation | Stroke IschemicItaly
Clinical Trials on Web-Based Star Cancellation Test
-
NHS Greater Glasgow and ClydeUnknown
-
Andrew Pouw, MDTerminated
-
Royal Brompton & Harefield NHS Foundation TrustKing's College Hospital NHS Trust; Imperial College LondonCompletedCystic Fibrosis | Hearing Loss, SensorineuralUnited Kingdom
-
St Joseph University, Beirut, LebanonNot yet recruitingBalance Performance
-
Clínica BazterricaWithdrawn
-
University of SouthamptonCompletedType 2 Diabetes
-
Inje UniversityCompleted
-
NYU Langone HealthStanford University; Shaare Zedek Medical CenterCompletedAnxiety Disorders | Major Depression | Post Traumatic Stress DisorderIsrael
-
Arizona State UniversityUniversity of Colorado, Denver; University of New MexicoUnknownChildhood Obesity | Childhood OverweightUnited States
-
Seattle Children's HospitalCompletedChronic Pain | Headache | Central SensitisationUnited States