Length of time periods in treatment effect descriptions and willingness to initiate preventive therapy: a randomised survey experiment
- PMID: 30458757
- PMCID: PMC6247706
- DOI: 10.1186/s12911-018-0662-2
Length of time periods in treatment effect descriptions and willingness to initiate preventive therapy: a randomised survey experiment
Abstract
Background: Common measures used to describe preventive treatment effects today are proportional, i.e. they compare the proportions of events in relative or absolute terms, however they are not easily interpreted from the patient's perspective and different magnitudes do not seem to clearly discriminate between levels of effect presented to people.
Methods: In this randomised cross-sectional survey experiment, performed in a Swedish population-based sample (n = 1041, response rate 58.6%), the respondents, aged between 40 and 75 years were given information on a hypothetical preventive cardiovascular treatment. Respondents were randomised into groups in which the treatment was described as having the effect of delaying a heart attack for different periods of time (Delay of Event, DoE): 1 month, 6 months or 18 months. Respondents were thereafter asked about their willingness to initiate such therapy, as well as questions about how they valued the proposed therapy.
Results: Longer DoE:s were associated with comparatively greater willingness to initiate treatment. The proportions accepting treatment were 81, 71 and 46% when postponement was 18 months, 6 months and 1 month respectively. In adjusted binary logistic regression models the odds ratio for being willing to take therapy was 4.45 (95% CI 2.72-7.30) for a DoE of 6 months, and 6.08 (95% CI 3.61-10.23) for a DoE of 18 months compared with a DoE of 1 month. Greater belief in the necessity of medical treatment increased the odds of being willing to initiate therapy.
Conclusions: Lay people's willingness to initiate preventive therapy was sensitive to the magnitude of the effect presented as DoE. The results indicate that DoE is a comprehensible effect measure, of potential value in shared clinical decision-making.
Keywords: Medical decision-making; Necessity-concern framework; Risk communication; Risk perception.
Conflict of interest statement
Ethics approval and consent to participate
Respondents gave informed consent to participation by returning a filled in questionnaire, and the study was approved by the ethical committee at the regional Ethical Committee of Clinical Investigation in Uppsala, with project identification code DNR 2013/269.
Consent for publication
Not applicable.
Competing interests
All the authors declare that there is no potential competing interest.
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References
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- WHO . Adherence to Long-term Therapies: Evidence for action. Geneva: World Health Organization; 2003.
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