Las Vergnas, Olivier · Journal of participatory medicine · 2017 · DOI
This paper examines different ways that patients and patient organizations can participate in health research. The authors created a framework to classify and compare these different types of involvement, from minimal participation to patients being equal partners in designing and running studies. They found that when patient organizations are actively involved, research tends to be more thoughtful and reflective—especially important for conditions like ME/CFS where traditional medical testing may not capture the full picture.
ME/CFS research has historically lacked adequate patient involvement and lacks reliable biomedical markers, making patient-centered and participatory research approaches essential. This framework provides researchers and patient organizations with a structured way to design and evaluate research that genuinely incorporates patient expertise and lived experience. For the ME/CFS community, this work validates the importance of patient organization involvement in shaping research priorities and methodologies.
This study does not evaluate the effectiveness or outcomes of different participation models in actually improving research quality or patient health. It is a descriptive methodological analysis based on literature review, not an empirical trial comparing different participation schemes. The framework does not establish which specific participation model is optimal for ME/CFS research specifically.
About the PEM badge: “PEM required” means post-exertional malaise was an explicit required diagnostic criterion for participant inclusion in this study — not that PEM was studied, observed, or discussed. Studies using criteria that do not require PEM (e.g. Fukuda, Oxford) are tagged “PEM not required”. How the atlas works →
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