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Compensatory reading training for people with homonymous visual field defects

Compensatory reading training for people with homonymous visual field defects - Reading training in hemianopia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON51525
Enrollment
135
Registered
2022-06-24
Start date
2021-05-10
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

halfsided blindness Partial cortical blindness

Interventions

Sponsors

Rijksuniversiteit Groningen
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria: * Homonymous visual field defect (at least a quadrantanopia, either right-sided or left-sided) due to acquired post-chiasmatic brain injury * At least three months between onset HVFD and the first measurement * Near visual acuity >= 0.5 with patient*s own current correction * MMSE score >=24 * Age >= 18 years * Presence of by patient formulated treatment goal regarding reading

Exclusion criteria

Exclusion criteria: A subject who meets any of the following criteria will be excluded from participation in this study: * Additional visual field defect (at least cluster) in ipsilesional visual hemi-field * Pre-existing dyslexia/ illiteracy/ low literacy/ other pre-morbid reading problems * No clear neurological cause of HVFD * Presence of comorbid neglect The following criteria are made on the premise that, when present, they will impair the ability to successfully followthe intervention: * Communication difficulties (e.g. severe hearing impairment, no fluent understanding of Dutch language, severeaphasia as indicated by the Token test) * Negative advice of treatment team regarding reading intervention participation, due to e.g. severe psychiatric, cognitive or visual perception disorders, problems with health, motivation or illness awareness or misuse ofdrugs/alcohol/medication * Additional visual disturbances (e.g. diplopia, metamorphopsia, low contrast sensitivity)

Design outcomes

Primary

MeasureTime frame
The primary outcome measures of this study reflect reading performance as well as perceived reading performance: Words per minute read out loud (((number of words read-number of errors)/time [s]) x 60), Number of reading errors, Words per minute read silently ((number of words in paragraph/time [s]) x 60), Subjective report on reading behavior and participation (index scores), Subjective report on reading difficulties.

Secondary

MeasureTime frame
Vision-related quality of life questionnaire, Fatigue questionnaire, Training motivation, Reading history, Education,Sustained attention task, Working memory task, Long-term memory task, Executive functioning task

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)