The Stroke Vision App: A Screening Tool for Visual Stroke

NCT02539381 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 62

Last updated 2015-09-03

No results posted yet for this study

Summary

Visual impairment can affect up to 70% of stroke survivors, but many do not have their vision adequately assessed in hospital. An unidentified visual defect can cause significant problems for recovery and quality of life. The Stroke Vision app (an application currently scaled for a 10" Android tablet) has been developed to act as a screening tool for visual problems in stroke survivors; to help identify visual problems earlier and thereby improve rehabilitation outcomes. The app includes a suite of tests for assessing the patient's acuity, their visual fields and to aid in the identification of visual neglect / inattention. Furthermore, it includes educational information on visual stroke in order to better educate staff, patients and their carers. This study seeks to validate the novel digital assessments included in the Stroke Vision app against the current methods used for screening (clinical examination by confrontation field testing). Both screening measures will be compared with the gold standard methods for visual assessments, Octopus perimetry for fields and paper-based methods for visuospatial neglect

Conditions

Interventions

PROCEDURE

Formal Perimetry (Goldman or Octopus visual Field)

PROCEDURE

Albert's visual inattention test

PROCEDURE

Star cancellation visual inattention test

PROCEDURE

Visual field assessment to confrontation

PROCEDURE

Visual inattention assessment to bilateral stimuli

DEVICE

Digital tumbling E visual accuity assessment

DEVICE

Digital visual field assessment

DEVICE

Digital line crossing assessment

DEVICE

Digital shape cancellation assessment

Sponsors & Collaborators

  • NHS Greater Glasgow and Clyde

    lead OTHER

Principal Investigators

  • Christine McAlpine, MBChB FRCP · NHS Greater Glasgow & Clyde

Study Design

Allocation
RANDOMIZED
Purpose
SCREENING
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-07-31
Primary Completion
2016-01-31
Completion
2016-01-31

Countries

  • United Kingdom

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02539381 on ClinicalTrials.gov