The Patient Reported Inventory of Self-Management of Chronic Conditions (PRISM-CC): testing for bias across patient characteristics and languages
- PMID: 41493704
- PMCID: PMC12774984
- DOI: 10.1007/s11136-025-04124-5
The Patient Reported Inventory of Self-Management of Chronic Conditions (PRISM-CC): testing for bias across patient characteristics and languages
Keywords: Chronic disease; Differential item functioning; Differential test functioning; Measurement invariance; Patient reported outcome measure; Self-management.
Plain language summary
Health providers and researchers often use questionnaires and surveys to help make decisions, such as who needs treatment or what kind of treatment they need. Misleading or wrong decisions can be made if the tools are not well designed. This study was done to test whether a new tool called the Patient Reported Inventory of Self-Management of Chronic Conditions works equally well for men and women, older and younger people, and those with different levels of education and different numbers of conditions. It also tested whether the tool worked well in English and Swedish. The tool has 36 questions answered by patients, with results showing seven areas that people might find hard to manage. Over 1500 people from around the world provided data for this study. The results show that this tool yields comparable results across different types of patients in either English or Swedish.
Conflict of interest statement
Declarations. Conflict of interest: The authors have no relevant financial interests to disclose. However, the PRISM-CC has been developed and is owned by TP, GK and ÅA. Ethical approval: The Healthy Ageing Initiative (HAI) study has received ethical approval from the Swedish Ethical Review Authority and the Regional Ethics Review Board in Umeå in 2007 (Dnr 2012-85-32 M- and dnr 07-031 M), and a complementary ethical application for this project was approved by the Regional Ethics Review Board in Umeå in 2020 (Dnr 2020–02387). This study was performed in agreement with the principles of the Declaration of Helsinki. Consent to participate: Written informed consent was obtained from all participants. Consent for publication: Not applicable.
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References
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