MS-DETECT: Early Detection of Multiple Sclerosis Progression With MSCopilot® Detect
Launched by AD SCIENTIAM · Apr 3, 2023
Trial Information
Current as of September 14, 2025
Active, not recruiting
Keywords
ClinConnect Summary
The MS-DETECT trial is studying a smartphone app called MSCopilot® Detect, which is designed to help patients with Multiple Sclerosis (MS) monitor their symptoms from home. The main goal of the study is to improve how doctors can track the progression of MS, whether it's due to relapses (sudden worsening of symptoms) or gradual changes over time. Researchers also want to make sure the app is safe and easy to use, and they aim to see if it can detect changes in a patient's condition early on.
To participate in the study, you need to be an adult aged 30 to 65 with a specific type of MS and certain levels of disability that have been stable for the last three months. You'll need to have a smartphone that meets certain requirements and be comfortable using it. If you join, you'll participate in a few visits over two years, where you'll fill out questionnaires about your symptoms and quality of life, and complete digital tests to help track your condition. The study is currently recruiting participants in several countries, including the United States, Canada, and various European nations.
Gender
ALL
Eligibility 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.
About Ad Scientiam
Ad Scientiam is a leading clinical trial sponsor dedicated to advancing medical research through innovative digital health solutions. With a focus on developing and validating cutting-edge technologies, the company aims to enhance patient engagement and data accuracy in clinical studies. By harnessing real-world data and leveraging artificial intelligence, Ad Scientiam strives to accelerate the drug development process while ensuring compliance with regulatory standards. Their commitment to scientific rigor and patient-centric approaches positions them as a pivotal player in the evolution of clinical research.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Lille, France
Dresden, Germany
Toronto, Canada
Milan, Italy
Oklahoma City, Oklahoma, United States
Esbjerg, Denmark
Madrid, Spain
Atlanta, Georgia, United States
Indianapolis, Indiana, United States
Columbus, Ohio, United States
Oklahoma City, Oklahoma, United States
Burnaby, Canada
Ottawa, Canada
Vancouver, Canada
Glostrup, Denmark
Kolding, Denmark
Viborg, Denmark
Lomme, France
Marseille, France
Nice, France
Rouen, France
Bayreuth, Germany
Böblingen, Germany
Erbach, Germany
Bari, Italy
Florence, Italy
Foggia, Italy
Roma, Italy
Girona, Spain
Madrid, Spain
Málaga, Spain
Oviedo, Spain
Zaragoza, Spain
Erbach, Germany
Málaga, Spain
San Diego, California, United States
Northbrook, Illinois, United States
New Orleans, Louisiana, United States
St Louis, Missouri, United States
Portland, Oregon, United States
Austin, Texas, United States
Glostrup, Denmark
Girona, Spain
Patients applied
MZ
TG
KT
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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