Author
Listed:
- Julie Y L Chow
- Hilary J Don
- Ben Colagiuri
- Evan J Livesey
Abstract
Associative learning models have traditionally simplified contingency learning by relying on binary classification of cues and outcomes, such as administering a medical treatment (or not) and observing whether the patient recovered (or not). While successful in capturing fundamental learning phenomena across human and animal studies, these models are not capable of representing variability in human experiences that are common in many real-world contexts. Indeed, where variation in outcome magnitude exists (e.g., severity of illness in a medical scenario), this class of models, at best, approximate the outcome mean with no ability to represent the underlying distribution of values. In this paper, we introduce one approach to incorporating a distributed architecture into a prediction error learning model that tracks the contingency between cues and dimensional outcomes. Our Distributed Model allows associative links to form between the cue and outcome nodes that provide distributed representation depending on the magnitude of the outcome, thus enabling learning that extends beyond approximating the mean. Comparing the Distributed Model against a Simple Delta Model across four contingency learning experiments, we found that the Distributed Model provides significantly better fit to empirical data in virtually all participants. These findings suggest human learners rely on a means of encoding outcomes that preserves the continuous nature of experienced events, advancing our understanding of causal inference in complex environments.Author summary: When we learn about cause and effect in everyday life—such as whether a medicine helps recovery from illness—we experience outcomes that vary in degree rather than simply happening or not happening. Traditional models of how humans and animals learn have largely focused on these all-or-nothing scenarios, essentially tracking the average value when outcomes are dimensional. We developed a model that extends on simple error-correction models to represent how people learn about relationships between cues and outcomes that can take on a range of values. Instead of just tracking the average, our Distributed Model captures the full spectrum of possible outcomes and their frequencies. We tested this model against a conventional single point-estimate approach across four experiments and found that our Distributed Model better matched how people make predictions in nearly every case. Our findings suggest that a relatively simple adjustment to conventional prediction-error learning algorithms that allows representation of outcome magnitudes provide a powerful way to capture the information that we preserve when we learn about variable outcomes. This has important implications for understanding how people make predictions and decisions in real-world situations where outcomes naturally vary, from medical treatments to environmental changes.
Suggested Citation
Julie Y L Chow & Hilary J Don & Ben Colagiuri & Evan J Livesey, 2026.
"Predicting continuous outcomes: Some new tests of associative approaches to contingency learning,"
PLOS Computational Biology, Public Library of Science, vol. 22(6), pages 1-1, June.
Handle:
RePEc:plo:pcbi00:1013220
DOI: 10.1371/journal.pcbi.1013220
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pcbi00:1013220. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: ploscompbiol (email available below). General contact details of provider: https://journals.plos.org/ploscompbiol/ .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.