- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07415824
Multiple Sclerosis Implementation Network (Registry)
Multiple Sclerosis Implementation Network
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.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Amanda Montague, EdM
- Phone Number: 800-532-7667
- Email: AMontague@MYMSAA.org
Study Locations
-
-
New Jersey
-
Cherry Hill, New Jersey, United States, 08034
- Recruiting
- Multiple Sclerosis Association of America
-
Contact:
- Amanda Mantague, Ed.M.
- Phone Number: 800-532-7667
- Email: AMontague@MYMSAA.org
-
-
Texas
-
Austin, Texas, United States, 78712
- Recruiting
- The University of Texas at Austin
-
Contact:
- Leorah Freeman, MD, PhD
- Phone Number: (713) 992-9213
- Email: Leorah.Freeman@austin.utexas.edu
-
Houston, Texas, United States, 77030
- Recruiting
- The University of Texas Health Science Center at Houston (UTHealth Houston)
-
Contact:
- Maria E. Fernandez, PhD
- Phone Number: (713) 500-9626
- Email: Maria.E.Fernandez@uth.tmc.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- diagnosed with Multiple Sclerosis
- can speak and understand English comfortably
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Patients with Multiple Sclerosis
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Multiple sclerosis disability as assessed by the Patient-Determined Disease Steps (PDDS) Scale
Time Frame: 5 years
|
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
Time Frame: 5 years
|
Total score on the MSNQ ranges from 0 to 60, with a higher score indicating greater perceived cognitive impairment.
|
5 years
|
Collaborators and Investigators
Investigators
- Study Director: Amanda Montague, EdM, Multiple Sclerosis Association of America
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HSC-SPH-24-0515 (Registry)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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