The Maine Pain Registry, Pain Registry for ME 2, is a comprehensive, statewide chronic pain registry to advance epidemiological research and ultimately enhance healthcare practices in pain management throughout the state of Maine. The registry places a special focus on the influence of social determinants of health (SDOH) — the non-medical factors, such as racial/ethnic groups, education, income, employment, and housing environment — on chronic pain and its management, and is the first pain registry in the state.
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Mapping Pain Management In Maine Participant Flyer
Ling Cao
Flyer calling for participation in UNE project Mapping Pain Management in Maine.
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Pain Registry For ME 2 Participant Flyer
Ling Cao
Flyer calling for participation in UNE project Pain Registry for ME 2.
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Pain Registry For ME 2 Participant Information Sheet
Ling Cao
Information sheet for potential participants in UNE project Pain Registry for ME 2. Including: "Chronic pain is a serious public health problem but little is known about how pain affects Mainers. We plan to establish a pain registry through this study. This registry will collect information from Maine adults who experience recurrent and frequent pain. It is estimated that one...Read More