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Search / Trial NCT05816122

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.

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

3 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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