MS-DETECT: Early Detection of Multiple Sclerosis Progression With MSCo
MS-DETECT: Early Detection of Multiple Sclerosis Progression With MSCopilot® Detect
What it found
No result yet.
What was tested
Treatment tested
- MSCopilot® Detect mobile application
What it measured
Main measures
To evaluate MSCopilot® Detect individual scores and/or composite scores sensitivity to detect disability worsening based on revised-MSFC scores.
Throughout the study at each hospital visit: Day 0, Month 6, Month 12, Month 18 and Month 24 (if applicable)
Disability progressionHow the body handles the medicine
Other measures (14)
To evaluate MSCopilot® Detect individual scores and/or composite scores sensitivity to detect disability worsening based on EDSS.
Throughout the study at each hospital visit: Day 0, Month 6, Month 12, Month 18 and Month 24 (if applicable)
Disability progressionTo evaluate MSCopilot® Detect individual scores and/or composite scores sensitivity to detect disability worsening earlier than the EDSS.
Throughout the study at each hospital visit: Day 0, Month 6, Month 12, Month 18 and Month 24 (if applicable)
Disability progressionTo evaluate MSCopilot® Detect individual and/or composite scores ability to detect disease progression in absence of a relapsing activity (PIRA).
Throughout the study at each hospital visit: Day 0, Month 6, Month 12, Month 18 and Month 24 (if applicable)
Disability progressionRelapsesTo evaluate MSCopilot® Detect individual scores and/or composite scores ability to detect MSFC changes over time.
Throughout the study at each hospital visit: Day 0, Month 6, Month 12, Month 18 and Month 24 (if applicable)
Disability progressionTo measure MSCopilot® Detect individual scores and/or composite scores association with the clinical scores.
Throughout the study at each hospital visit: Day 0, Month 6, Month 12, Month 18 and Month 24 (if applicable)
Disability progressionWalking and mobilityTo assess reproducibility of MSCopilot® Detect individual scores and/or composite scores between in-clinic and at-home digital tests.
At home (Day 1, Month 6+1 day, Month 12 + 1 day, Month 18-1 day and Month 24-1 day (if applicable)) and in-clinic ((Day 0, Month 6, Month 12, Month 18 and Month 24 (if applicable))
To assess reliability of MSCopilot® Detect individual scores and/or composite scores at-home over time.
Day 0 versus Month 6, Month 6 versus Month 12, Month 12 versus Month 18, Month18 versus Month 24 (if applicable) AND Day 0 to Month 18 or Day 0 to Month 24 (if applicable) and Day 0 to Month 15 or Day
To evaluate Patient QoL (Multiple Sclerosis Impact Scale: MSIS-29 and Modified Fatigue Impact Scale - 5-item version: MFIS-5) and their association with MSCopilot® Detect individual and composite scores.
Throughout the study between in clinic visit, an average of 24 months
Disability progressionFatigueQuality of life (reported by participants)To evaluate the ability of MSCopilot® Detect individual scores and/or composite score to discriminate between a relapse and a momentary disability worsening (+1 point EDSS score for an initial EDSS <5,5; +0.5 point for an initial EDSS ≥5.5).
Throughout the study at each hospital visit: Day 0, Month 6, Month 12, Month 18 and Month 24 (if applicable)
Disability progressionRelapsesTo evaluate MSCopilot® Detect Safety
Throughout the study between in clinic visit, an average of 24 months
Safety
Who could take part
Relapsing and progressive · 30 to 65 · EDSS 2.5 to 6.5
Show the full criteria
Inclusion criteria
* Adult patients living with RRMS or SPMS, aged 30 to 65 * EDSS score between 2.5 to 6.5 points * With a disease duration > 5 years * Clinically stable during the last 3 months before inclusion (no relapses, no disability progression) * No change in the DMT* during the last 3 months before inclusion * Receiving optimal symptomatic treatments at baseline (clinician's judgment) * Owns a personal smartphone which mobile operating system is above 14 for IOS (iPhone) and 8 for Android included with a good internet connexion * Able to use a smartphone * Able to read language in wich the mobile application is available and able to understand pictograms. * Applicable to patients enrolled in France only: affiliated to a social security system.
Exclusion criteria
* Medically unstable conditions that may hinder patient's ability to comply with the study procedures * Inability to use a smartphone or MSCopilot® Detect application * Patient with corrected visual acuity less than 4/10 (Monoyer) or 20/50 (Snellen at 20 feet) or +0,4 (LogMAR) * Pregnancy and nursing women * Persons under guardianship or curatorship * Current drugs or/and alcohol abuse that could influence performance on the tests (clinician's judgment) * Patients have participated in another clinical study within the previous 30 days of screening or are currently participating in another study that, in the opinion of the Investigator, might interfere with the patient's full participation in the study or confound the assessment of the patient or outcome of the study.
As registered. Criteria can change, so ask the trial team or your neurologist.
About this trial
In the sponsor's words
The study aims to evaluate MSCopilot® Detect, a smartphone application for at-home monitoring of patients with Multiple Sclerosis (MS). The primary objective is to enhance and standardize remote monitoring of MS patients to accurately assess disease progression caused by either Relapse Activity Worsening (RAW) or Progression Independent of Relapses (PIRA). The study also aims to assess the safety, usability, and satisfaction of the solution. A secondary objective is to determine MSCopilot® Detect's ability to provide early detection of disease changes and predict changes in Expanded Disability Status Scale (EDSS) scores in more patients. Exploratory objectives include evaluating the relationship between MSCopilot® Detect composite and individual scores and other biomarkers such as MRI, soluble glial fibrillary acidic protein (sGFAP), and soluble neurofilament light chain (sNfL). Patients will be able to download the free MSCopilot® Detect app. They will participate in 1 inclusion visit and 3 follow-up visits, scheduled at 6 months, 12 months, and 18 months (an additional visit at 24 months may be scheduled if necessary). Every 3 months, patients will complete validated questionnaires regarding MS symptoms and quality of life and participate in digital tests designed to monitor MS symptom progression. The study will include 336 MS patients and will be conducted in the United States, Canada, Germany, Italy, Spain, Denmark and France
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History
Started
Sept 2023
Main results due
May 2027
Finished
May 2027