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Scanning behaviour in hemianopia: The Next Step

Scanning behaviour in hemianopia: The Next Step - The Next Step

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON52952
Enrollment
55
Registered
2021-08-12
Start date
2021-11-11
Completion date
Unknown
Last updated
2025-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Partial cortical blindness partial visual field defect

Interventions

None listed

Sponsors

Clinical and developmental neuropsychology
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: For patients participating in the test sessions: - Homonymous visual field defect (at least a quadrantanopia, either right-sided or left-sided) due to acquired post-chiasmatic brain injury (based on binocular perimetry) - At least three months between onset HVFD and the first measurement. -Written consent including permission to obtain data from the patient file at Visio. For all subjects participating in the test sessions: - Age >=18 years. - Able to walk at least 50 meters independently or by using a cane/rollator, without a wheelchair (mobility assessment has to be possible). - Binocular visual acuity 0.5 or higher using current correction. - Eye and head mobility undisturbed in all directions. - MMSE score >= 24. The inclusion criteria to participate in the training sessions for patients with HH are: Age >= 18 years Homonymous visual field defect.

Exclusion criteria

Exclusion criteria: In the test sessions: a participant meeting any of the following criteria will be excluded from the study: - An additional visual field defect in the ipsilesional visual hemi-field. - Additional visual disturbances (e.g. impaired contrast sensitivity, diplopia, oscillopsia, metamorphopsia). - No clear neurological cause of HVFD. - An indication of severe higher order visual perception disorders, such as visual agnosia, severe unilateral neglect, or Bálint*s Syndrome. - Severe psychiatric, cognitive or visual perception disorders. - Misuse of drugs/alcohol/medication. - Severe hearing impairment: hearing aids allowed (verbal communication should be possible). - Problems with balance or orientation impairing mobility. - Impairments in understanding or communicating Dutch (spoken) language. There are no exclusion criteria for patients with HH participating in the training sessions.

Design outcomes

Primary

MeasureTime frame
Eye movement parameters: fixations (location, duration) and saccades (direction, amplitude) and task performance (e.g. number of errors, reaction time) during mobility and search tasks.

Secondary

MeasureTime frame
Neuropsychological paramters, visual parameters, and outcomes of three questionnaires and semi-structured interviews to evaluate VR + eye-tracking.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)