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. 2024 Jan 18;27(1):e13970. doi: 10.1111/hex.13970

Table 1.

Document characteristics (n = 65).

Document characteristic N %
Year of publication
2012–2013 3 5%
2014–2015 1 2%
2016–2017 7 11%
2018–2019 8 12%
2020–2021 26 40%
2022 5 8%
Undated 15 23%
Country of origin
Canada 37 57%
United Kingdom 17 26%
United States of America 8 12%
Switzerland 2 3%
Belgium 1 2%
Document source organisation (select all that apply)
Research network 29 45%
Government organisation (i.e., agency established by national or provincial government) 15 23%
Health or academic institution 15 23%
Charity or foundation 6 9%
Nongovernmental organisations 4 6%
Government (e.g., Ministry of Health) 2 3%
Target audience (select all that apply)
Researcher 35 54%
Patient partner 27 42%
Policy maker 9 14%
Researcher representative 5 8%
Industry member 3 5%
Unclear 15 23%
Level of policy‐making
National 33 51%
Provincial or state‐specific 15 23%
Subprovincial/state 4 6%
International 3 5%
Unclear 10 15%
Document scope
Focused on patient engagement with a section dedicated to compensation 30 46%
Focused on patient partner compensation 30 46%
General research guidance with a section on patient partner compensation 4 6%
Focused on compensation with a section dedicated to patient partners 1 2%