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临床试验/NCT05061953
NCT05061953招募中不适用

Development of a Novel Functional Eye-Tracking Software Application for Multiple Sclerosis

Innodem Neurosciences2 个研究点 分布在 1 个国家目标入组 168 人开始时间: 2021年10月18日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
168
试验地点
2
主要终点
Change from Baseline in Symbol Digit Modalities Test (SDMT) score at Month 48

研究概览

简要总结

This study aims to develop and validate a sensitive and non-invasive eye-tracking software application.

This study will obtain participant responses to brief cognitive tests designed to evaluate several key functions known to be affected by MS and non-invasive eye movement measurements in response to visually presented stimuli during specifically designed eye-tracking tests. The study data will be used to develop machine learning algorithms and validate a software application intended to track the progressive component of multiple sclerosis and associated cognitive changes.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Able to provide informed consent.
  • Aged 18 years or older at the time of enrollment.
  • Able to read in either French or English.
  • Visual acuity of 20/100 in at least one eye (corrective glasses, contact lenses, surgery etc.
  • are permitted)
  • For patients only:
  • Confirmed diagnosis of MS with no signs of progressive increase in physical disability within the past six months.
  • Neurological condition is medically stable during the study visit.
  • Expanded Disability Status Scale (EDSS) score 0 - 8.0 at the initial visit.

排除标准

  • Evidence or medical history of psychiatric issues that are known to also affect movements and oculomotor control.
  • Presence of co-morbid neurological conditions to avoid eye movement anomaly confounds (Strabismus, cranial nerve palsy, stroke-causing hemianopsia).
  • Diagnosis of macular edema or other pre-existing ocular conditions that would prevent a participant from performing the eye movement assessments.
  • Recent (less than three months from enrollment) start of, change of dose, or irregular use of, new prescription drugs known to influence ocular motor visual function, such as benzodiazepines, antipsychotics and anticonvulsants. Occasional use of benzodiazepines for medical procedures is permitted, at the investigator's discretion, but should not occur within a short time period prior to or during an eye movement assessment.
  • For healthy controls only:
  • Evidence or history of significant neurodegenerative disorder affecting brain function, e.g., multiple sclerosis (MS), Parkinson's disease (PD), Amyotrophic lateral sclerosis (ALS), Dementia.
  • For MS patients only
  • Diagnosis of Clinically Isolated Syndrome (CIS), Radiologically Isolated Syndrome (RIS) or Primary Progressive MS (PPMS).
  • Patients who are currently experiencing a relapse or who have experienced a relapse within the last three months. A relapse is defined as appearance of a new neurological abnormality or worsening of previously stable or improving pre-existing neurological abnormality, separated by at least 30 days from onset of a preceding clinical demyelinating event (McDonald et al. 2001). The abnormality must have been present for at least 24 hours and occurred in the absence of fever (< 37.5°C) or known infection.
  • Patients who have been undergoing disease-modifying therapy for less than three months

结局指标

主要结局

Change from Baseline in Symbol Digit Modalities Test (SDMT) score at Month 48

时间窗: Baseline and Month 48

The SDMT is used to assess divided attention, visual scanning, tracking and motor speed. Using a reference key, the examinee has 90 seconds to pair specific numbers with given geometric figures. Scoring involves summing the number of correct substitutions within the 90 second interval.

次要结局

  • Change from Baseline in the Multiple sclerosis functional composite (MSFC) scores at Month 48(Baseline and Month 48)
  • Change from Baseline in the Expanded Disability Status Scale (EDSS) score at Month 48(Baseline and Month 48)
  • Change from Baseline in the Brief International Cognitive Assessment for MS (BICAMS) scores at Month 48(Baseline and Month 48)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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