NCT04735406Completed
The MS-LINK™ Outcomes Study
The MS-LINK™ Outcomes Study: A Comprehensive Prospective Longitudinal Assessment of Patient and Clinical Reported Outcomes in Multiple Sclerosis Patients Across North America
Source: ClinicalTrials.gov · Last updated 22 Aug 2024
Brief summary (registry, in English)
The Multiple Sclerosis (MS) Leadership and Innovation Network (MS-LINK™) is comprised of networks working cooperatively to advance Multiple Sclerosis (MS) science and improve MS participant outcomes. In this study participants will be followed from the time of consent through the lifetime of the study (currently 3 years), unless the participant chooses to withdraw from the study. Collection of participant's medical history, including MS and treatment history, will be automated through extraction from the participant's electronic medical record (EMR) and other health information systems (for example, radiology). Participants will complete patient-reported outcomes (PROs) and other health-related information digitally. Participating participants will have access to their own data in an ongoing manner via a web-based Participant Portal.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 2182 (actual)
- First submitted
- 28 Jan 2021
- Start date
- 24 Mar 2021
- Primary completion date
- 31 Jan 2024
- Lead sponsor
- EMD Serono Research & Development Institute, Inc.
- Diseases
- Multiple sclerosis
- NCT number
- NCT04735406
What you commit to
- Study type: Observational
- Participants enrolled: 2182
- From 24 Mar 2021 to the primary completion date, 31 Jan 2024
- 9 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
- Participants participating in interventional clinical drug trials at baseline
Other
- Unable to complete questionnaires in English
- Unable to consistently access the Internet
Who the study is looking for
- Participants willing and able to provide written informed consent
- Participants willing to be contacted while participating in the study for recruitment into sub-studies that may be relevant to them
- Participants willing and able to complete PROs on a monthly basis and document events of interest as they occur
- Participants willing to participate in additional follow up at the site for at least three years
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (9)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Atlanta Neuroscience Institute Coordinator of this site? Confirm its status | Atlanta | United States | Unknown status |
| The University of Texas of Austin Coordinator of this site? Confirm its status | Austin | United States | Unknown status |
| Alabama Neurology Associates Coordinator of this site? Confirm its status | Birmingham | United States | Unknown status |
| Beth Israel Deaconess Medical Center Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
| The Oklahoma Medical Research Foundation Coordinator of this site? Confirm its status | Oklahoma City | United States | Unknown status |
| University of Nebraska Medical Center Coordinator of this site? Confirm its status | Omaha | United States | Unknown status |
| Memorial Healthcare Coordinator of this site? Confirm its status | Owosso | United States | Unknown status |
| University of Texas Health Coordinator of this site? Confirm its status | San Antonio | United States | Unknown status |
| Georgetown University Coordinator of this site? Confirm its status | Washington D.C. | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.