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
- Diseases
- Multiple sclerosis
- 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
Sites (34)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Galina Vorobeychik Coordinator of this site? Confirm its status | Burnaby | Canada | Unknown status |
| Mark Freedman Coordinator of this site? Confirm its status | Ottawa | Canada | Unknown status |
| St. Michael's Hospital Coordinator of this site? Confirm its status | Toronto | Canada | Unknown status |
| Robert Carruthers Coordinator of this site? Confirm its status | Vancouver | Canada | Unknown status |
| Boris-Alexander Kallman Coordinator of this site? Confirm its status | Bayreuth | Germany | Unknown status |
| Universitätsklinikum Carl Gustav Carus Coordinator of this site? Confirm its status | Dresden | Germany | Unknown status |
| Rupert Knoblich Coordinator of this site? Confirm its status | Erbach im Odenwald | Germany | Unknown status |
| University Hospital of Southern Denmark Coordinator of this site? Confirm its status | Esbjerg | Denmark | Unknown status |
| Finn Sellebjerg Coordinator of this site? Confirm its status | Glostrup Municipality | Denmark | Unknown status |
| Sivagini Prakash Coordinator of this site? Confirm its status | Viborg | Denmark | Unknown status |
| Gary Álvarez Bravo Coordinator of this site? Confirm its status | Girona | Spain | Unknown status |
| University Hospital San Carlos Coordinator of this site? Confirm its status | Madrid | Spain | Unknown status |
| Enric Monreal Coordinator of this site? Confirm its status | Madrid | Spain | Unknown status |
| Ana Alonso Coordinator of this site? Confirm its status | Málaga | Spain | Unknown status |
| Miguel Llaneza Coordinator of this site? Confirm its status | Oviedo | Spain | Unknown status |
| Jesùs Martin Coordinator of this site? Confirm its status | Zaragoza | Spain | Unknown status |
| Hopital Roger Salengro Coordinator of this site? Confirm its status | Lille | France | Unknown status |
| Cécile Donzé Coordinator of this site? Confirm its status | Lomme | France | Unknown status |
| Adil Maarouf Coordinator of this site? Confirm its status | Marseille | France | Unknown status |
| Mikael Cohen Coordinator of this site? Confirm its status | Nice | France | Unknown status |
| Bertrand Bourre Coordinator of this site? Confirm its status | Rouen | France | Unknown status |
| Emilio Portaccio Coordinator of this site? Confirm its status | Florence | Italy | Unknown status |
| Emanuele D'Amico Coordinator of this site? Confirm its status | Foggia | Italy | Unknown status |
| IRCCS Ospedale San Raffaele Coordinator of this site? Confirm its status | Milan | Italy | Unknown status |
| Joash Lazarus Sr. Coordinator of this site? Confirm its status | Atlanta | United States | Unknown status |
| Leorah Freeman Coordinator of this site? Confirm its status | Austin | United States | Unknown status |
| Aaron Boster Coordinator of this site? Confirm its status | Columbus | United States | Unknown status |
| Craig E. Herrman Coordinator of this site? Confirm its status | Indianapolis | United States | Unknown status |
| Jennifer Feng Coordinator of this site? Confirm its status | New Orleans | United States | Unknown status |
| Daniel Wynn Coordinator of this site? Confirm its status | Northbrook | United States | Unknown status |
| Gabriel Pardo Coordinator of this site? Confirm its status | Oklahoma City | United States | Unknown status |
| Vijayshree Yadav Coordinator of this site? Confirm its status | Portland | United States | Unknown status |
| Jennifer Graves Coordinator of this site? Confirm its status | San Diego | United States | Unknown status |
| Robert Naismith Coordinator of this site? Confirm its status | St Louis | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.