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NCT05816122Active, not recruiting

MS-DETECT: Early Detection of Multiple Sclerosis Progression With MSCopilot® Detect

Source: ClinicalTrials.gov · Last updated 3 Nov 2026

Brief summary (registry, in English)

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

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
336 (actual)
First submitted
13 Mar 2023
Start date
22 Sept 2023
Primary completion date
31 May 2027
Lead sponsor
Ad scientiam
NCT number
NCT05816122

What you commit to

  • Study type: Interventional
  • Participants enrolled: 336
  • From 22 Sept 2023 to the primary completion date, 31 May 2027
  • 34 sites in 7 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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.

Other illness

  • Medically unstable conditions that may hinder patient's ability to comply with the study procedures

Other

  • 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

Who the study is looking for

  • 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.

Age in the registry: 30 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (34)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Galina Vorobeychik
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BurnabyCanadaUnknown status
Mark Freedman
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OttawaCanadaUnknown status
St. Michael's Hospital
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TorontoCanadaUnknown status
Robert Carruthers
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VancouverCanadaUnknown status
Boris-Alexander Kallman
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BayreuthGermanyUnknown status
Universitätsklinikum Carl Gustav Carus
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DresdenGermanyUnknown status
Rupert Knoblich
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Erbach im OdenwaldGermanyUnknown status
University Hospital of Southern Denmark
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EsbjergDenmarkUnknown status
Finn Sellebjerg
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Glostrup MunicipalityDenmarkUnknown status
Sivagini Prakash
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ViborgDenmarkUnknown status
Gary Álvarez Bravo
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GironaSpainUnknown status
University Hospital San Carlos
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MadridSpainUnknown status
Enric Monreal
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MadridSpainUnknown status
Ana Alonso
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MálagaSpainUnknown status
Miguel Llaneza
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OviedoSpainUnknown status
Jesùs Martin
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ZaragozaSpainUnknown status
Hopital Roger Salengro
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LilleFranceUnknown status
Cécile Donzé
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LommeFranceUnknown status
Adil Maarouf
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MarseilleFranceUnknown status
Mikael Cohen
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NiceFranceUnknown status
Bertrand Bourre
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RouenFranceUnknown status
Emilio Portaccio
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FlorenceItalyUnknown status
Emanuele D'Amico
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FoggiaItalyUnknown status
IRCCS Ospedale San Raffaele
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MilanItalyUnknown status
Joash Lazarus Sr.
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AtlantaUnited StatesUnknown status
Leorah Freeman
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AustinUnited StatesUnknown status
Aaron Boster
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ColumbusUnited StatesUnknown status
Craig E. Herrman
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IndianapolisUnited StatesUnknown status
Jennifer Feng
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New OrleansUnited StatesUnknown status
Daniel Wynn
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NorthbrookUnited StatesUnknown status
Gabriel Pardo
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Oklahoma CityUnited StatesUnknown status
Vijayshree Yadav
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PortlandUnited StatesUnknown status
Jennifer Graves
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San DiegoUnited StatesUnknown status
Robert Naismith
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St LouisUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.