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Dig deeper into ACP’s capabilities through fact sheets, case studies, publications, presentations, and examples of our work.

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Fact sheets and case studies

Everything you need to evaluate a partnership with ACP.

Cover image of ACP fact sheet: Partner with ACP

Overview of ACP Resources

An overview of ACP's integrated research ecosystem, including biosamples, community engagement, and inclusive research expertise.

Cover of ACP Fact Sheet: ACP Repository, Data and Samples

ACP Biosamples and Data

A deep dive into the ACP Repository: biospecimens, longitudinal data, multi-omics datasets, and the DNAnexus analysis platform.

Cover of ACP Fact Sheet: iConquerMS for Researchers

iConquerMS for Researchers

How researchers can tap into ACP's people-powered network of 10,000+ people affected by MS across every phase of a study.

Cover for ACP Fact Sheet: Research Dissemination

Research Dissemination

How ACP helps researchers share findings with the MS community through lay summaries, infographics, podcasts, and more.

Cover of ACP Fact Sheet: Your Partner for Inclusive Research

Partnering for Inclusive Research

An intro to the RIDE Council and MREPN, ACP's two complementary resources for making MS research more representative and inclusive.

Cover of the "How to partner with ACP" flyer

How to Partner with ACP

See how a research partnership with ACP works, from initial conversation through project launch, along with starting costs for iConquerMS and other research services.

Cover of ACP Fact Sheet: Case Study on ACP and COVID-19 Rapid Research

Case Study: Rapid Insights in a Crisis

How ACP and Massachusetts General Hospital went from concept to published findings in five months during the COVID-19 pandemic.

Cover of ACP Fact Sheet: Case Study on the Power of a Patient Council

Case Study: The Power of a Patient Council

How ACP and EMD Serono built a year-long patient council that directly shaped clinical trial design and development strategy.

Publications

Peer-reviewed research from ACP and our partners.

Cover of The Patient journal

Patient Engagement in Research

Eight expectations for engaging the people research is intended to serve throughout the research process.

Cover of Biological Research for Nursing

Sex Differences in MS

Differential microRNA expression reveals sex-specific neuroinflammatory and neurodegenerative signatures in relapsing-remitting multiple sclerosis

Cover of Maturitas journal

Menopause and MS

A scoping review of symptoms, disease course, and lived experience

JMIR Research Protocols journal

User-Centered Protocol Designs

Adaptation of the transition readiness assessment questionnaire for pediatric-onset multiple sclerosis: Protocol for a user-centered design approach

Cover of Neurology Journal

COVID-19

COVID-19 Vaccination Reactogenicity in Persons With Multiple Sclerosis

ACP posters & presentations

Conference presentations from ACP researchers and partners.

Poster of COVID-19 study

COVID-19

Humoral and Cellular Immune Responses to COVID-19 across DMTs in a Decentralized MS Cohort

Poster of A Review of the Current Landscape of Disease-Modifying Therapy Continuation, De-Escalation, and Discontinuation in Older Adults with MS

Aging with MS

A Review of the Current Landscape of DMT Continuation, De-Escalation, and Discontinuation in Older Adults with MS

Image of poster: Co-creation o a Prioritized Research Agenda for Pediatric MS

Pediatric MS

Co-Creation of a Prioritized Research Agenda for Pediatric MS

Inclusive research toolkits and resources

Built by the MS Minority Research Engagement Partnership Network. Available to all.

MS Minority in research toolkit

Toolkit for Research Professionals

Guidance and best practices for recruiting and engaging underrepresented communities in MS research.

Close up of a man wearing a black sports watch typing on a laptop.

Inclusive Research Resources

A searchable catalog of articles, videos, and tools on MS health equity and research engagement.

MS minority in research clinician toolkit

Toolkit for Healthcare Professionals

Guidance and tools for talking with patients from underrepresented communities about MS research participation.

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