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Not yet recruitingNCT06629155VisuMSUpdated Nov 6, 2024

Studying Eye Movement Deficits and Cognitive Impairment in Patients with Multiple Sclerosis Using Infrared Eye Tracking and Cognitive Tests

An observational study in Multiple Sclerosis and Internuclear Ophthalmoplegia, sponsored by Universitair Ziekenhuis Brussel. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-11-06.

Sponsored by Universitair Ziekenhuis Brussel · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
50
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this observational study is to study the relationship between cognitive problems and problems in eye movements in Multiple Sclerosis (MS).

The main questions it aims to answer are:

  • What is the correlation between eye movement parameters (VDI AUC and VDI Pv/Am, left and right) and SDMT scores in patients with MS?
  • What is the number of patients with VDI AUC>1.174 and/or VDI Pv/Am>1.180 assessed by infrared oculography during prosaccades at 15 degrees left or right?
  • What is the correlation between eye movement parameters (VDI AUC and VDI Pv/Am, left and right) and cognitive test scores in patients with MS?

Participants will perform specific cognitive tests and eye movements will be measured through infrared oculography.

The primary hypothesis for the study is: participants who exceed the treshold (VDI AUC>1.174 and/or VDI Pv/Am>1.180, left or right) will perform worse on cognitive tests compared to those who don't.

Read the detailed description

As previously described in the brief summary, this clinical study aims to investigate the relationship between cognitive impairment and eye movement parameters in Multiple Sclerosis (MS).

Cognitive tests

Cognitive impairment is a common symptom in patients with MS. The most affected cognitive domains are information processing speed and visual memory, but also the domains of attention, executive function, working memory, visuospatial processing and verbal memory can be affected. There are different valid screening and evaluation tools for cognitive impairment (CI) described and used in the MS field. This clinical study will use the tests of the Brief International Cognitive Assessment for MS (BICAMS).

Infrared oculography

Another common symptom in MS is problems with eye movements. An eye condition commonly seen in these patients is internuclear ophthalmoplegia (INO). It is a specific conjugate horizontal gaze disorder characterized by slowed movement of the adducting eye relative to the abducting eye in horizontal saccades, resulting from damage to the medial longitudinal fasciculus (MLF). This may lead to (transient) diplopia or 'blurring of vision', particularly during horizontal gaze. INO can be diagnosed by using infrared oculography, a noninvasive method of quantifying eye movements. Recent research indicates that eye movements can reflect certain aspects of brain function and provide insights into cognitive impairments. Therefore, this study aims to investigate the prevalence of INO in MS using infrared oculography, compare the diagnosis of INO using infrared oculography with clinical examination by a physician and lastly explore the relationship between the presence of INO and cognitive decline.

Investigational plan

The study will be a prospective observational multi-center, cross-sectional cohort study.

Patients will be recruited at the National MS Center Melsbroek (NMSC) in close collaboration with Prof. Miguel D'haeseleer (Neurology), Prof. Daphne Kos (Rehabilitation and research coordinator) and Mieke D'hooge (Neuropsychologist). At any moment in time about 80 MS patients are in a short rehabilitation admission at the National MS Centre Melsbroek. Additionally, patients will be recruited from the MS department in the neurology wing of UZ Brussels. The MS team at UZ Brussel comprises Prof. Dr. Ir. Guy Nagels (Head of Departement), Prof. Dr. Miguel D'Haeseleer, Prof. Dr. Marie D'Hooghe, Dr. Stéphanie Hostenbach, and Annick Van Merhaegen.

When patients fulfill the inclusion criteria and give active informed consent, they will be contacted by phone to schedule their visit. If patients would like more information they can contact the investigator by phone.

During their visit, patients will undergo cognitive testing and infrared oculography. The investigators will start with the cognitive assessments, which include the BICAMS and the PASAT. The BICAMS is a 15-minute-long neuropsychological evaluation battery (9). The PASAT typically lasts 15-20 minutes. Altogether, the cognitive testing will take around 40 minutes. Following this, the infrared oculography measurements will be done. According to a study that provided a standardized and reproducible protocol for infrared oculography measurements, the total experiment duration was 21 minutes, excluding instructions. Thus, the oculography process will take roughly 30 minutes. To ensure enough time for each patient and avoid rushing, the total duration of the visit will be approximately 1,5 hours per patient.

After their first visit, there is no need for a follow-up. Should any questions arise afterward, they are welcome to reach out to us via phone or email.

Patients may withdraw from the study at any time for any reason.

Quality assurance plan/ data checks

After measurement, the variables that are needed for analysis have to be imported into Matlab. The analysis will be automated and checked for quality issues by researchers. To pass quality control, at least 50% of prosaccades at 15 degrees must be captured.

Source data verification To ensure accuracy and completeness, two researchers will evaluate and verify the source data. Any discrepancies will be documented and managed in line with the Good Clinical Practice guidelines.

Data dictionary

INO will be quantified through eye movement parameters Cognitive scores will be recorded.

Clinical parameters that will be recorded:

  • EDSS score, a numeric value between 0 and 10
  • Age, a numeric value > 18
  • Disease duration, a numeric value (years)
  • Sex, female or male

Standard Operating Procedures (SOPs)

Only the investigators will be responsible for data entry. As previously described, the analysis will be automated and checked for quality issues by researchers.

All data will be collected, encrypted, analyzed and stored on a dedicated sharepoint using the One Drive cloud service provided by the VUB, secured by password protection. All files from this server will be removed 5 years after the end of publication of the research results.

Sample size assessment

The investigators will use a one-tailed alpha of 0.05 (as the hypothesis is that worse visual scanning will relate to worse cognitive scores), a power of 0.8 (0.2 Type II error rate), and a correlation coefficient of 0.4 - corresponding to 16% of the variance of the SDMT being explained by eyesight - which leads to a sample size of 37. To be on the safe side and to account for possible data quality issues, the investigators will recruit N = 50 patients in this study.

Plan for missing data

In the exceptional case that some parameters are missing for some patients, those patients will be excluded from the specific analyses for which these datapoints are needed.

Statistical analyses plan

The correlation between eye movement parameters (VDI Pv/Am and VDI AUC, left and right), and cognitive test scores will be analyzed through Spearman correlation analysis.

02

Conditions studied

  • Multiple Sclerosis
  • Internuclear Ophthalmoplegia

Keywords

  • Cognitive impairment
  • Multiple Sclerosis
  • Internuclear Ophthalmoplegia
  • SDMT
03

In context

Multiple Sclerosis

3,267 studies on the registry are indexed under Multiple Sclerosis; 662 are open to participants now.

This study's planned enrollment of 50 is below the median of 100 across 971 observational studies indexed under Multiple Sclerosis.

Browse Multiple Sclerosis studies →

Lead sponsor

Universitair Ziekenhuis Brussel is the lead sponsor of 375 studies on the registry; 107 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

MS patients recruited from the neurology department of UZ Brussels and NMSC Melsbroek in Belgium

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Diagnosed with clinically definite multiple sclerosis according to the 2017 McDonald criteria
  • At least 18 years old
  • Combined vision with optimal correction > 0,6 on Snellen Visual Acuity Test.
  • Providing .

Exclusion criteria

Exclusion criteria:

  • Major medical or psychiatric pathology that potentially affects cognitive functioning.
  • A score higher than 63 on the Fatigue Scale for Motor and Cognitive Functions is categorized as severe fatigue
  • Start or switch in immunomodulatory treatment within three months before inclusion.
  • Less than 3 months post exacerbation.
  • Refusing .
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
50 participants (estimated)
Patient registry
No

Groups and cohorts

  • People with multiple sclerosis

    This study will include 50 people with MS (see in/exclusion criteria under "Eligibility").

    Diagnostic Test: Infrared oculography

Interventions

  • Diagnostic testInfrared oculography

    Eye movements will be captured through infrared oculography and processed via in-house algorithms.

06

What researchers measure

Primary outcomes

  1. Correlation between eye movement parameters and SDMT.

    Correlation between eye movement parameters (VDI AUC and VDI Pv/Am, left and right) and SDMT scores in patients with MS.

    Time frame: baseline

Secondary outcomes

  1. Number of patients with eye movement abnormalities assessed by infrared oculography

    The number of patients with VDI AUC\>1.174 and/or VDI Pv/Am\>1.180 assessed by infrared oculography during prosaccades at 15 degrees left or right.

    Time frame: Baseline

  2. Correlation between eye movement parameters and cognitive test scores.

    The cognitive tests used to asses this correlation include the following: the PASAT (Paced Auditory Serial Addition Task), the CVLT-II (California Verbal Learning Test-II) and the BVMT-R (Brief Visuospatial Memory Test Revised). The correlation between eye movement parameters parameters (VDI Pv/Am and VDI AUC, left and right), and cognitive test scores will be analyzed through Spearman correlation analysis.

    Time frame: Baseline

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Beier M, Gromisch ES, Hughes AJ, Alschuler KN, Madathil R, Chiaravalloti N, Foley FW. Proposed cut scores for tests of the Brief International Cognitive Assessment of Multiple Sclerosis (BICAMS). J Neurol Sci. 2017 Oct 15;381:110-116. doi: 10.1016/j.jns.2017.08.019. Epub 2017 Aug 16. PubMed 28991659 ↗
  • Meca-Lallana V, Gascon-Gimenez F, Ginestal-Lopez RC, Higueras Y, Tellez-Lara N, Carreres-Polo J, Eichau-Madueno S, Romero-Imbroda J, Vidal-Jordana A, Perez-Miralles F. Cognitive impairment in multiple sclerosis: diagnosis and monitoring. Neurol Sci. 2021 Dec;42(12):5183-5193. doi: 10.1007/s10072-021-05165-7. Epub 2021 Apr 1. PubMed 33796947 ↗
  • Van Schependom J, D'hooghe MB, Cleynhens K, D'hooge M, Haelewyck MC, De Keyser J, Nagels G. The Symbol Digit Modalities Test as sentinel test for cognitive impairment in multiple sclerosis. Eur J Neurol. 2014 Sep;21(9):1219-25, e71-2. doi: 10.1111/ene.12463. Epub 2014 May 22. PubMed 24850580 ↗
  • Nij Bijvank JA, Petzold A, Balk LJ, Tan HS, Uitdehaag BMJ, Theodorou M, van Rijn LJ. A standardized protocol for quantification of saccadic eye movements: DEMoNS. PLoS One. 2018 Jul 16;13(7):e0200695. doi: 10.1371/journal.pone.0200695. eCollection 2018. PubMed 30011322 ↗
  • Nij Bijvank JA, Hof SN, Prouskas SE, Schoonheim MM, Uitdehaag BMJ, van Rijn LJ, Petzold A. A novel eye-movement impairment in multiple sclerosis indicating widespread cortical damage. Brain. 2023 Jun 1;146(6):2476-2488. doi: 10.1093/brain/awac474. PubMed 36535900 ↗
  • Nij Bijvank JA, van Rijn LJ, Balk LJ, Tan HS, Uitdehaag BMJ, Petzold A. Diagnosing and quantifying a common deficit in multiple sclerosis: Internuclear ophthalmoplegia. Neurology. 2019 May 14;92(20):e2299-e2308. doi: 10.1212/WNL.0000000000007499. Epub 2019 Apr 19. PubMed 31004067 ↗

Individual participant data

Plan to share: Undecided

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Mar 2025; primary completion for Feb 2027, 23 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 1, 2024
First posted
Oct 8, 2024
StartEst.
Mar 1, 2025
Primary completionEst.
Feb 1, 2027
CompletionEst.
Feb 1, 2027
Last update
Nov 6, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Nov 6, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06629155
Responsible party
Jeroen Van Schependom (Research Professor, Universitair Ziekenhuis Brussel) — Principal investigator
First posted
Oct 8, 2024
Start date
Mar 1, 2025 (estimated)
Primary completion
Feb 1, 2027 (estimated)
Completion
Feb 1, 2027 (estimated)
Last update
Nov 6, 2024

Study contacts

Jeroen Van Schependom, PhD in Medical Sciences
Contact
jeroen.van.schependom@vub.be
0032 6291040

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2024. You cannot join it, but the record below documents what was studied.

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