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

NCT07830745 — Not applicable, Not yet recruiting, 30 participants, Clinique Les Trois Soleils

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RegistryNCT07830745, acronym OPTO
StatusNot yet recruiting
PhaseNot applicable
Study typeInterventional; randomized, crossover, masking: single, treatment
Enrollment30 (Estimated)
SponsorClinique Les Trois Soleils (Other); collaborators: Laboratoire Mémoire Cerveau et Cognition, Boulogne-Billancourt, France
ConditionsHemianopia Homonymous, Stroke
InterventionsOptokinetic stimulation without reading task, Optokinetic stimulation with reading task (Other)
Datesstart 2026-10-01 (estimated), primary completion 2027-06-01 (estimated), completion 2027-06-01 (estimated), first posted 2026-09-21, last updated 2026-09-21
Locations1 site in France

Related Papers Related Patents Related Grants Related Experts
All trials for Hemianopia Homonymous All trials for Stroke All trials of Optokinetic stimulation without reading task All trials of Optokinetic stimulation with reading task

-Summary

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.

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+Detailed description

Stroke can cause a visual field defect known as homonymous hemianopia (HH). When this visual field loss involves the macula, the central area of vision, it may result in reading difficulties known as hemianopic alexia (HA).

The literature reports improved reading performance in these patients after repeated induction of horizontal optokinetic nystagmus (i.e., an oculomotor reflex consisting of horizontal saccades). To induce this nystagmus, previous studies have used a reading task involving text scrolling from right to left.

However, this type of exercise, which relies on reading, is cognitively demanding and may lead to frustration due to reading difficulties, fatigue, and reduced motivation and potentially the impact of rehabilitation. Therefore, the use of a non-reading task could help overcome these limitations.

The present study aims to compare the efficacy of optokinetic stimulation with reading to optokinetic stimulation without reading in patients with HA.

+Arms and interventions

ArmTypeInterventionsDescription
Group AOtherOther: Optokinetic stimulation without reading task; Other: Optokinetic stimulation with reading taskPatients receive 15 sessions of optokinetic rehabilitation with a reading task, followed by 15 sessions of optokinetic rehabilitation without an associated reading task. The optokinetic rehabilitation sessions with reading are considered the standard of care, while optokinetic rehabilitation without an associated reading task is the experimental condition. Each patient undergoes both conditions sequentially and serves as their own control.
Group BOtherOther: Optokinetic stimulation without reading task; Other: Optokinetic stimulation with reading taskPatients receive 15 sessions of optokinetic rehabilitation without an associated reading task, followed by 15 sessions of optokinetic rehabilitation with a reading task. The optokinetic rehabilitation sessions with reading are considered the standard of care, while optokinetic rehabilitation without an associated reading task is the experimental condition. Each patient undergoes both conditions sequentially and serves as their own control.
  • Optokinetic stimulation without reading task (Other): 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): 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.

+Outcome measures

Primary outcomes

  • Change in reading speed on paper [Baseline and end of each 4-week rehabilitation period: Week 0, Week 4, and Week 8]: 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.

Secondary outcomes

  • Change in reading accuracy on paper [Baseline and end of each 4-week rehabilitation period: Week 0, Week 4, and Week 8]: Change in the number and type of errors (paralexias, omissions) assessed using the International Reading Speed Texts (IReST).
  • Change in reading speed on screen [Baseline and end of each 4-week rehabilitation period: Week 0, Week 4, and Week 8]: Change in the number of correctly read words per minute, assessed using a screen-based reading task
  • Change in reading accuracy on screen [Baseline and end of each 4-week rehabilitation period: Week 0, Week 4, and Week 8]: Change in the number and type of errors (paralexias, omissions), assessed during a screen-based reading task
  • Change in subjective reading abilities [Baseline and end of each 4-week rehabilitation period: Week 0, Week 4, and Week 8]: Change in the score on the Hemianopia Reading Questionnaire (HRQ)
  • Change in ocular fixations during reading [Baseline and end of each 4-week rehabilitation period: Week 0, Week 4, and Week 8]: Change in the number of fixations and in the mean fixation duration (in ms) during the screen-based reading task, assessed with an eyetracker
  • Change in ocular saccades during reading [Baseline and end of each 4-week rehabilitation period: Week 0, Week 4, and Week 8]: Change in the number and in the mean amplitude of saccades (in degrees) during the screen-based reading task, assessed with an eyetracker
  • Change in optokinetic nystagmus [Baseline and at the end of both rehabilitation: Week 0 and Week 8]: Change of saccade amplitude and frequency during optokinetic stimulation
  • Change in visual detection during standard perimetry [Baseline and end of each 4-week rehabilitation period: Week 0, Week 4, and Week 8]: Change in visual sensitivity (in dB) at each tested visual field location on automated static perimetry (Humphrey or Octopus)
  • Change in visual detection during screen-based perimetry [Baseline and end of each 4-week rehabilitation period: Week 0, Week 4, and Week 8]: Change in number of correctly detected targets and mean reaction time (in ms) at each tested visual field location on screen-based perimetry
  • Tolerability of rehabilitation [Before and after each rehabilitation session]: Score of fatigue, stress, and mood induced by the treatment, self-assessed using a numbered visual analogue scale
  • Motivation for rehabilitation [End of each 4-week rehabilitation period: Week 4 and Week 8]: Score obtained on the Situational Motivation Scale

+Eligibility

Sex: All, ages: 18 Years to any

Inclusion Criteria:

* Time since lesion > 1 month
* Diagnosis of homonymous hemianopia post-stroke without macular sparing
* Reading complaint and/or reading impairment
* Proficiency in reading French
* Agreed to give informed consent
* Afiliated with national health insurance

Exclusion Criteria:

* 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)
* Instability of reading impairment
* Instability of homonymous hemianopia
* Major cognitive that would limit the ability of the patient to participate in the study (unilateral spatial neglect, simultanagnosia, comprehension disorder, oral expression disorder)

+Locations (1)

FacilityCityCountryStatus
Clinique Les Trois SoleilsBoissise-le-Roi, Île-de-France RegionFrance

+Publications

  • Goodwin D. Homonymous hemianopia: challenges and solutions. Clin Ophthalmol. 2014 Sep 22;8:1919-27. doi: 10.2147/OPTH.S59452. eCollection 2014. PMID 25284978
  • Schuett S, Heywood CA, Kentridge RW, Zihl J. Rehabilitation of hemianopic dyslexia: are words necessary for re-learning oculomotor control? Brain. 2008 Dec;131(Pt 12):3156-68. doi: 10.1093/brain/awn285. Epub 2008 Nov 3. PMID 18984602
  • Zihl J. Eye movement patterns in hemianopic dyslexia. Brain. 1995 Aug;118 ( Pt 4):891-912. doi: 10.1093/brain/118.4.891. PMID 7655887
  • Spitzyna GA, Wise RJ, McDonald SA, Plant GT, Kidd D, Crewes H, Leff AP. Optokinetic therapy improves text reading in patients with hemianopic alexia: a controlled trial. Neurology. 2007 May 29;68(22):1922-30. doi: 10.1212/01.wnl.0000264002.30134.2a. PMID 17536049

+Investigators

  • Christophe Duret, Principal investigator, Clinique Les Trois Soleils, Boissise-le-Roi, France