MS patients and doctors team up to fix fragmented care
NCT ID NCT07289724
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aims to understand how to better coordinate care for people with multiple sclerosis (MS). Researchers will hold focus groups with patients, carers, and healthcare professionals to identify what works and what doesn't in current care pathways. The goal is to propose improvements that make the healthcare journey less confusing and more effective for everyone involved.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could point toward better care pathways that make it easier for people with MS to navigate the healthcare system.
- What could go wrong
- This is a small, early-stage observational study with only 57 participants, so findings may not apply to all MS patients or healthcare settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 57 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
erson diagnosed with MS, carer for someone with MS, Healthcare professional working with MS patients.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Person diagnosed with MS; * Carer for someone with MS; * Healthcare professional working with MS patients; * Adult; * Person who has not objected to participating in the research. Exclusion Criteria: * Any person who has objected to the use of their data.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Paris
RECRUITINGParis, 75013, France
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