NCT06922942Completed
MSCopilot Users' Feedback in Real Life - Outcomes Regarding Integration in Patients' pathWay and Users' ExpeRience
MS-FLOWER: MSCopilot Users' Feedback in Real Life - Outcomes Regarding Integration in Patients' pathWay and Users' ExpeRience
Source: ClinicalTrials.gov · Last updated 2 Nov 2026
Brief summary (registry, in English)
This US multicenter, prospective cohort study aims to evaluate how MSCopilot can be seamlessly integrated into the current care pathway and identify potential optimizations to enhance its impact on both MS patients and clinicians, facilitating broader implementation. Specifically, the study will assess: * The overall integration of MSCopilot into routine clinical practice, * Patients' ability to use MSCopilot at home without supervision, * The need for patient support when using MSCopilot at home, * User behavior based on usage analytics data from the MSCopilot mobile app and dashboard, * Patient adherence to MSCopilot use in routine clinical practice, * The adequacy of the onboarding/training process for HCPs, * The effectiveness of HCPs onboarding/training in ensuring successful patient onboarding, * The variances in user behavior and adherence to MSCopilot use according to socio-demographic factors and EDSS scores
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 62 (actual)
- First submitted
- 1 Apr 2025
- Start date
- 12 Aug 2025
- Primary completion date
- 27 Apr 2026
- Lead sponsor
- Ad scientiam
- Diseases
- Multiple sclerosis
- NCT number
- NCT06922942
What you commit to
- Study type: Interventional
- Participants enrolled: 62
- From 12 Aug 2025 to the primary completion date, 27 Apr 2026
- 4 sites in 1 country
- 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
- Patient who previously participated in a study using MSCopilot
- Early termination criteria (for patients):
Other
- Pregnant and nursing women
- Person under guardianship or curatorship
- Inability to use a smartphone application
- exclusion criteria,
- death,
- abandon,
- loss of follow-up,
- investigator's decision
Who the study is looking for
- For patients
- 18 years and older
- With a confirmed and documented MS diagnosis, per the 2010 Revised
- McDonald criteria
- With an EDSS score ranging from 0 to 6.5
- Able to monitor their disease from home (i.e. not hospitalized or under medical assistance).
- Having a personal smartphone with a mobile operating system above 16 for IOS (iPhone) and 8 for Android and having access to a good internet connection.
- Able to read language in which the mobile application is available and able to understand pictograms Having read the information sheet and signed the informed consent form
- For HCPs:
- Licensed neurologists trained in the management of Multiple Sclerosis patients and allowed to conduct clinical studies within their departments
- If applicable: nurses or medical assistants specifically trained in the management of Multiple Sclerosis and allowed to participate in clinical studies within their departments
- Ability to use a computer
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Leorah Freeman Coordinator of this site? Confirm its status | Austin | United States | Unknown status |
| Jenny Feng Coordinator of this site? Confirm its status | New Orleans | United States | Unknown status |
| Gabriel Pardo Coordinator of this site? Confirm its status | Oklahoma City | 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.