Numerical self-report scales are extensively used in economics, psychology, and even medicine to quantify subjective feelings, ranging from life satisfaction to the experience of pain. These scales are often criticized for lacking an objective foundation, and defended on the grounds of empirical performance. We focus on the case of pain measurement, where existing self-reported measures are the workhorse but known to be inaccurate and difficult to compare across individuals. We provide a new measure, inspired by standard economic elicitation methods, that quantifies the negative value of acute pain in monetary terms, making it comparable across individuals. In three preregistered studies, 330 healthy participants were randomly allocated to receive either only a high- or only a low-pain stimulus or a high-pain stimulus after having double-blindly received a topical analgesic or a placebo. In all three studies, the new measure greatly outperformed the existing self-report scales at distinguishing whether participants were in the more or the less painful condition, as confirmed by effect sizes, Bayesian factor analysis, and regression-based predictions.
Competing Interest StatementThe authors have declared no competing interest.
Clinical TrialNCT05415423
Clinical ProtocolsFunding StatementThe study was funded by the University research budget of Carlos Alos-Ferrer. No external funding was received.
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
The studies were approved by the Cantonal Ethics Committee in Zurich (BASEC: 2022-00236).
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityDe-identified participants data and the code for the analyses is publicly available in OSF
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