Clinical trial Recruiting at 3 sites Observational Ages 18 and up

Multiple Sclerosis Implementation Network Registry

Official title: Multiple Sclerosis Implementation Network

Run by The University of Texas Health Science Center, Houston · NCT07415824 · Data updated 2026-11-12

This registry collects electronic health records and patient information to see if sharing data across clinics improves care and quality of life for people with multiple sclerosis.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment2000 (estimated)
SponsorThe University of Texas Health Science Center, Houston
Academic / other
Locations3 sites (Cherry Hill, New Jersey and 2 other locations)
StatusRecruiting
StartedApril 28, 2025
Main results expectedDecember 31, 2030
Study endsDecember 31, 2030
Registry record updatedFebruary 17, 2026
Trial IDNCT07415824 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are people diagnosed with multiple sclerosis who can comfortably read and speak English and who are willing to allow their health records from participating providers to be included in the registry.

Probably not a fit

People without MS, those who cannot communicate in English, or individuals unwilling to share medical records are unlikely to benefit from or be eligible for this registry.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The Multiple Sclerosis Implementation Network (MSIN) is a collaborative registry that links participant electronic health records from multiple providers and institutions. It brings together clinicians, people with MS, advocacy organizations, and researchers in implementation science to identify and spread effective care practices. Participants agree to allow integration of their medical records and may provide additional information to support projects focused on care delivery and outcomes. The registry supports testing and dissemination of innovations aimed at making MS care more consistent and effective across sites.

Why it matters

Potential benefit: If successful, the registry could speed uptake of best practices across clinics and improve health outcomes and quality of life for people with MS.

How similar studies have gone: Other disease registries and MS-focused implementation projects have helped identify care gaps and improve practice patterns, so this approach builds on established methods.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* diagnosed with Multiple Sclerosis
* can speak and understand English comfortably

Where it's running

  • Multiple Sclerosis Association of America
    Cherry Hill, New Jersey, United States
    Recruiting
  • The University of Texas at Austin
    Austin, Texas, United States
    Recruiting
  • The University of Texas Health Science Center at Houston (UTHealth Houston)
    Houston, Texas, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.