Your browser doesn't support javascript.
loading
The Swiss Multiple Sclerosis Registry (SMSR): study protocol of a participatory, nationwide registry to promote epidemiological and patient-centered MS research.
Steinemann, Nina; Kuhle, Jens; Calabrese, Pasquale; Kesselring, Jürg; Disanto, Giulio; Merkler, Doron; Pot, Caroline; Ajdacic-Gross, Vladeta; Rodgers, Stephanie; Puhan, Milo Alan; von Wyl, Viktor.
Afiliación
  • Steinemann N; Epidemiology, Biostatistics and Prevention Institute, University of Zurich, Hirschengraben 84, CH-8001, Zurich, Switzerland.
  • Kuhle J; Neurological Policlinic, University Hospital Basel, Basel, Switzerland.
  • Calabrese P; Department of Psychology, University of Basel, Basel, Switzerland.
  • Kesselring J; Rehabilitation Clinic Valens, Valens, Switzerland.
  • Disanto G; Department of Neurology, Regional Hospital Lugano (EOC), Lugano, Switzerland.
  • Merkler D; Division of Clinical Pathology, Geneva University Hospital, Geneva, Switzerland.
  • Pot C; Department of Clinical Neuroscience, Centre hospitalier universitaire vaudois, Lausanne, Switzerland.
  • Ajdacic-Gross V; Epidemiology, Biostatistics and Prevention Institute, University of Zurich, Hirschengraben 84, CH-8001, Zurich, Switzerland.
  • Rodgers S; Epidemiology, Biostatistics and Prevention Institute, University of Zurich, Hirschengraben 84, CH-8001, Zurich, Switzerland.
  • Puhan MA; Epidemiology, Biostatistics and Prevention Institute, University of Zurich, Hirschengraben 84, CH-8001, Zurich, Switzerland.
  • von Wyl V; Epidemiology, Biostatistics and Prevention Institute, University of Zurich, Hirschengraben 84, CH-8001, Zurich, Switzerland. viktor.vonwyl@uzh.ch.
BMC Neurol ; 18(1): 111, 2018 Aug 13.
Article en En | MEDLINE | ID: mdl-30103695
ABSTRACT

BACKGROUND:

Multiple sclerosis (MS) is one of the most frequently observed neurological conditions in Switzerland, but data sources for country-wide epidemiological trend monitoring are lacking. Moreover, while clinical and laboratory MS research are generally well established, there is a gap in patient-centered MS research to inform care management, or treatment decisions and policy making not only in Switzerland but worldwide.

METHODS:

In light of these research gaps, the Swiss Multiple Sclerosis Society initiated and funded the Swiss Multiple Sclerosis Registry (SMSR) an open-ended, longitudinal and prospective, nationwide, patient-centered study. The SMSR recruits adult persons with a suspected or confirmed MS diagnosis who reside or receive care in Switzerland. The SMSR has established a governance structure with clear rules and guidelines. It follows a citizen-science approach with direct involvement of persons with MS (PwMS), who contribute actively to registry development, operations, and research. Main scientific goals entail the study of MS epidemiology in Switzerland, health care access and provision, as well as life circumstances and wellbeing of persons with MS. The innovative study design ("layer model") offers several participation options with different time commitments. Data collection is by means of regular surveys and medical record abstraction. Survey participation is offered in different modes (web, paper & pencil) and in the three main national languages (German, French, Italian). Participants also receive regular data feedbacks for personal use and self-monitoring, contextualized in the whole population of study participants. Data feedbacks are also used to solicit data corrections of key variables from participants.

DISCUSSION:

The SMSR combines the advantages of traditional and novel research methods in medical research and has recruited over 1600 PwMS in its first year. The future-oriented design and technology will enable a response not only to future technological innovations and research trends, but also to challenges in health care provision for MS. TRIAL REGISTRATION ClinicalTrials.gov NCT02980640 ; December 6, 2016; retrospectively registered.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Participación del Paciente / Sistema de Registros / Atención Dirigida al Paciente / Investigación Biomédica / Esclerosis Múltiple Tipo de estudio: Guideline / Observational_studies / Prognostic_studies / Qualitative_research Límite: Adolescent / Adult / Humans País/Región como asunto: Europa Idioma: En Revista: BMC Neurol Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Participación del Paciente / Sistema de Registros / Atención Dirigida al Paciente / Investigación Biomédica / Esclerosis Múltiple Tipo de estudio: Guideline / Observational_studies / Prognostic_studies / Qualitative_research Límite: Adolescent / Adult / Humans País/Región como asunto: Europa Idioma: En Revista: BMC Neurol Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Suiza