NCT07415824

Brief Summary

The Multiple Sclerosis Implementation Network (MSIN) is a collaboration between the Multiple Sclerosis Association of America (MSAA), The University of Texas Health Science Center at Houston (UTHealth Houston), Dell Medical School at The University of Texas at Austin, and Novartis Pharmaceuticals Corporation. The goal of MSIN is to improve Multiple Sclerosis (MS) care, patient health, and quality of life through the development and support of implementation research and clinical practice collaboration. MSIN brings together healthcare teams, people with MS, and research leaders in MS and implementation science (IS) to learn, share, test, implement, and disseminate innovations that improve MS care, patient health, and quality of life. This ClinicalTrials.gov record pertains to the MSIN Patient Registry, which is a comprehensive database that integrates participants' electronic health records from various providers.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,000

participants targeted

Target at P75+ for all trials

Timeline
56mo left

Started Apr 2025

Longer than P75 for all trials

Geographic Reach
1 country

3 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress19%
Apr 2025Dec 2030

Study Start

First participant enrolled

April 28, 2025

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

January 29, 2026

Completed
19 days until next milestone

First Posted

Study publicly available on registry

February 17, 2026

Completed
4.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2030

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2030

Last Updated

February 17, 2026

Status Verified

January 1, 2026

Enrollment Period

5.7 years

First QC Date

January 29, 2026

Last Update Submit

February 9, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Multiple sclerosis disability as assessed by the Patient-Determined Disease Steps (PDDS) Scale

    Total score on the PDDS ranges from 0 (normal) to 8 (Bedridden: Unable to sit in a wheelchair for more than one hour), with a higher score indicating a worse outcome.

    5 years

  • Perception of cognitive impairment as assessed by the Multiple Sclerosis Neuropsychological Questionnaire (MSNQ) Scale

    Total score on the MSNQ ranges from 0 to 60, with a higher score indicating greater perceived cognitive impairment.

    5 years

Study Arms (1)

Patients with Multiple Sclerosis

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Clinics in the United States treating MS patients.

You may qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

Multiple Sclerosis Association of America

Cherry Hill, New Jersey, 08034, United States

RECRUITING

The University of Texas at Austin

Austin, Texas, 78712, United States

RECRUITING

The University of Texas Health Science Center at Houston (UTHealth Houston)

Houston, Texas, 77030, United States

RECRUITING

MeSH Terms

Conditions

Multiple Sclerosis

Condition Hierarchy (Ancestors)

Demyelinating Autoimmune Diseases, CNSAutoimmune Diseases of the Nervous SystemNervous System DiseasesDemyelinating DiseasesAutoimmune DiseasesImmune System Diseases

Study Officials

  • Amanda Montague, EdM

    Multiple Sclerosis Association of America

    STUDY DIRECTOR

Central Study Contacts

Amanda Montague, EdM

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Target Duration
2 Years
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

January 29, 2026

First Posted

February 17, 2026

Study Start

April 28, 2025

Primary Completion (Estimated)

December 31, 2030

Study Completion (Estimated)

December 31, 2030

Last Updated

February 17, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations