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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02486562
Other study ID # ACP-MS-PPRN-001
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 2014
Est. completion date October 2036

Study information

Verified date April 2024
Source Accelerated Cure Project for Multiple Sclerosis
Contact Sara Loud, MSEE, MBA
Phone 781-487-0032
Email sloud@acceleratedcure.org
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

iConquerMS™ is a research initiative developed by and for people with multiple sclerosis (MS) to contribute their health data and ideas to advance and accelerate research into MS.


Description:

The purpose of this study is to create a Multiple Sclerosis Patient-Powered Research Network (MS-PPRN) that includes at least 20,000 people with multiple sclerosis (MS) who contribute data on their health and other topics. Survey data will be made available to research scientists who are studying MS and similar diseases. Our goal is to use this data to answer questions that researchers and people with MS have regarding the disease, including its causes, treatments, and other topics. The MS-PPRN will be part of a national network for conducting research called PCORnet, the National Patient-Centered Clinical Research Network. PCORnet is supported by the Patient-Centered Outcomes Research Institute (PCORI). As the MS-PPRN is part of PCORnet, the data collected in surveys you complete may also be shared with researchers studying other diseases within the PCORnet network. While the MS-PPRN is focused on enrolling people with MS, people without MS are also welcome to participate in this research study. This study will be conducted online via the iConquerMS.org website. This is an ongoing study and will last for an indefinite period of time.


Recruitment information / eligibility

Status Recruiting
Enrollment 20000
Est. completion date October 2036
Est. primary completion date October 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria: - 21 years of age or older at the time of informed consent. Exclusion Criteria: - Unwilling or unable to provide informed consent.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Accelerated Cure Project Waltham Massachusetts

Sponsors (4)

Lead Sponsor Collaborator
Accelerated Cure Project for Multiple Sclerosis Arizona State University, Ogilvy, Patient-Centered Outcomes Research Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of people with multiple sclerosis who experience health-related quality-of-life changes 1 year
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