Effects of Optokinetic Stimulation Without a Reading Task in Patients With Hemianopic Alexia

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorClinique Les Trois Soleils

About this trial

The goal of this clinical trial is to investigate whether optokinetic stimulation delivered without a reading task can improve reading performance in adults with post-stroke hemianopic alexia. The main question it aims to answer is: does optokinetic stimulation without a reading task improve reading speed more than optokinetic stimulation with a reading task? Optokinetic stimlation with a reading task is considered the standard rehabilitation. These two conditions will be administered according to a randomized crossover design to determine wether the presence or absence of a reading task influences reading outcomes.

Participants will

* receive 4 weeks of optokinetic stimulation without a reading task and 4 weeks of optokinétic stimulation with a reading task, with the order of these two interventions determined by randomization, * undergo assesments of reading performance, oculomotor behavior, visual field and rehabilitation tolerability before and after each intervention period, * undergo a follow-up assesment 1 month after completion of the interventions.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Time since lesion > 1 month

Diagnosis of homonymous hemianopia post-stroke without macular sparing

Reading complaint and/or reading impairment

Proficiency in reading French

Disqualifiers

History of neurological or psychiatric disorders

Visual impairment of peripheral origin (i.e., related to damage to the structures of the eye or the optic nerve)

Uncorrected visual acuity deficit

Reading disorder prior to the stroke (dyslexia)

Trial design

Design model

Crossover

Treatments tested in this trial

  • Optokinetic stimulation without reading task

    Other intervention

    Participants are exposed to a horizontally moving optokinetic visual stimulus on a computer screen for 40 minutes per session. The task consists of viewing random sequences of letters scrolling from right to left. The sessions are spread out over 4 weeks, with 3 or 4 sessions per week, to achieve 10 hours (15 sessions) of optokinetic rehabilitation.

  • Optokinetic stimulation with reading task

    Other intervention

    Participants are exposed to a horizontally moving optokinetic visual stimulus on a computer screen for 40 minutes per session. The task consists of reading aloud sentences scrolling from right to left. The sessions are spread out over 4 weeks, with 3 or 4 sessions per week, to achieve 10 hours (15 sessions) of optokinetic rehabilitation. The scrolling speed ranges from 85 to 275 words per minute, depending on the participant's reading accuracy.

Treatment groups

30 Participants
are divided into 2 treatment groups
Group A: Group AOther 2 interventions
Group B: Group BOther 2 interventions

Trial outcomes

Primary outcomes

1

Change in reading speed on paper

Change in the number of correctly read words per minute, assessed using the International Reading Speed Texts (IReST). For each participant, the change in reading speed will be calculated separately for the optokinetic rehabilitation condition with a reading task and for the optokinetic rehabilitation condition without a reading task. The within-participant changes obtained after each 4-week period will be pooled across the two randomized sequences and compared between conditions. A higher reading speed indicates better reading performance.

Time frame
Baseline and end of each 4-week rehabilitation period: Week 0, Week 4, and Week 8

Secondary outcomes

1

Change in reading accuracy on paper

Change in the number and type of errors (paralexias, omissions) assessed using the International Reading Speed Texts (IReST).

Time frame
Baseline and end of each 4-week rehabilitation period: Week 0, Week 4, and Week 8
2

Change in reading speed on screen

Change in the number of correctly read words per minute, assessed using a screen-based reading task

Time frame
Baseline and end of each 4-week rehabilitation period: Week 0, Week 4, and Week 8
3

Change in reading accuracy on screen

Change in the number and type of errors (paralexias, omissions), assessed during a screen-based reading task

Time frame
Baseline and end of each 4-week rehabilitation period: Week 0, Week 4, and Week 8
4

Change in subjective reading abilities

Change in the score on the Hemianopia Reading Questionnaire (HRQ)

Time frame
Baseline and end of each 4-week rehabilitation period: Week 0, Week 4, and Week 8

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Clinique Les Trois Soleils

Lead sponsor

Laboratoire Mémoire Cerveau et Cognition, Boulogne-Billancourt, France

Collaborator

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