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July 18, 2012BMC Medical Informatics and Decision MakingOpen Access

The feasibility of collecting information from people with Multiple Sclerosis for the UK MS Register via a web portal: characterising a cohort of people with MS

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Population

People with Multiple Sclerosis in the UK

Design

Other

Authors

DFDavid FordSwansea UniversityKJKerina JonesSwansea UniversityRMRod MiddletonSwansea University

Discussion

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Implication

Supports web-based MS cohort characterization; leaves open scalability for research or clinical use.

Structured PICO

P
Population
People with Multiple Sclerosis in the UK
I
Intervention
Data collection via a web portal (UK MS Register)
O
Outcome
Feasibility of collecting data via a web platform

The UK MS Register web portal is a feasible method for collecting data to characterize cohorts of people with Multiple Sclerosis.

Cite This Study

Ford et al. (2012) studied this question.

synapsesocial.com/papers/69d9e6a6387cf70698685bd8https://doi.org/10.1186/1472-6947-12-73
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Also Consider

Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1A Gender Gap in Autoimmunity1999 · 860 citations
  2. 2Recommended diagnostic criteria for multiple sclerosis: Guidelines from the international panel on the diagnosis of multiple sclerosis2001 · 6,986 citations