IConquerMS™ - a Patient-Powered Research Network for Multiple Sclerosis

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02486562

Acronym

iCMS

Enrollment

20000

Registered

2015-07-01

Start date

2014-11-30

Completion date

2036-10-31

Last updated

2025-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis

Keywords

Multiple Sclerosis, MS

Brief 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. iConquerMS welcomes adults with MS and others interested in advancing MS research, children and teens with MS and their family members (via iConquerMS Kids & Teens) and MS caregivers (via iConquerMS Caregivers) to participate.

Detailed 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. While the MS-PPRN is focused on enrolling people with MS, people without MS are also welcome to participate in this research study. Adults are invited to participate via iConquerMS, while children and teens are invited to participate via iConquerMS Kids & Teens. Adults who are MS caregivers may participate via the dedicated iConquerMS Caregivers site. 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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

OTHER

Eligibility

Sex/Gender

ALL

Healthy volunteers

Yes

Inclusion criteria

* 21 years of age or older at the time of informed consent or under 21 with parental consent and participant assent.

Exclusion criteria

* Unwilling or unable to provide informed consent.

Design outcomes

Primary

Measure	Time frame
Number of people with multiple sclerosis who experience health-related quality-of-life changes	1 year

Countries

United States

Contacts

Primary ContactSara Loud, MSEE, MBA

sloud@acceleratedcure.org781-487-0032

Outcome results