Research priorities of patients with neuromuscular disease

Disabil Rehabil. 2013 Mar;35(5):405-12. doi: 10.3109/09638288.2012.694964. Epub 2012 Jul 2.


Purpose: This paper describes a study in which patients with neuromuscular disease (NMD) were engaged to list top-priorities for scientific research in order to complement the researchers' agenda.

Method: A dialogic model for research agenda setting was used. Interviews, focus groups and expert meetings with patients were held to identify research topics. Research topics were prioritized via a questionnaire. Agendas were integrated in a dialogue meeting with professionals and patients.

Results: The research agenda of NMD patients is divided in four research domains, with a total of 24 research topics. These domains include (1) health; (2) quality of life; (3)quality of care and support, and (4) basic issues. Among the research domains highest priority was given to research on health, followed by research on quality of life.

Conclusions: Both patients and professionals agreed a proper balance needs to be found between fundamental research and research on symptomatic treatment and quality of life. They concluded that more attention is required for research on the effective treatment of symptoms, quality of life and implementation of knowledge about NMD in regular care.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Female
  • Focus Groups
  • Health Priorities*
  • Health Services Needs and Demand*
  • Health Services Research / methods
  • Health Services Research / organization & administration*
  • Health Status
  • Humans
  • Interviews as Topic
  • Male
  • Needs Assessment
  • Neuromuscular Diseases / psychology*
  • Neuromuscular Diseases / therapy
  • Patient Participation*
  • Quality of Health Care
  • Quality of Life
  • Social Support
  • Surveys and Questionnaires