Fig. 4: Craving model comparison and parameter distribution: addictive condition.

a,b, As with decision models, ĪBIC was defined as the difference between each modelās BIC and the best-performing BIC in the alcohol group (a) and cannabis group (b). The joint outcomeā+āEV model performed best across groups. cāf, In the alcohol group, for the best performing craving model, we calculated the correlations between model-predicted craving and true craving ratings. An example alcohol participantās true (black line) versus predicted craving (blue line) is displayed. Two-sided one sample t test without correction was used for all significance testing (c). There was a high degree of correlation across participants in the alcohol group (mean r = 0.446), indicating strong model efficacy (d). Similarly, in the cannabis group, we visualize an example participantās true (black line) versus predicted craving (yellow line) (e). There was a high degree of correlation across participants in cannabis group (mean r = 0.446; f). g,h, Distributions of parameters were extracted from the outcomeā+āEV model. The left panel displays the joint distributions of outcome weight (\({w}_{\mathrm{outcome}}\)) and EV weight (\({w}_{\mathrm{EV}}\)), while craving baseline is visualized separately. In the alcohol group (g), \({w}_{\mathrm{outcome}}\) (tā=ā4.322, Pā<ā0.001) was significantly positive and \({w}_{\mathrm{EV}}\) (tā=āā0.256, Pā=ā0.798) was not significantly different from zero. In the cannabis group (h), neither parameter reached significance (\({w}_{\mathrm{outcome}}\), tā=ā1.603, Pā=ā0.114; \({w}_{\mathrm{EV}}\), tā=ā1.298, Pā=ā0.199). iāk, There were no significant group differences in baseline craving (tā=ā0.329, Pā=ā0.776) (i), outcome weight (tā=āā0.911, Pā=ā0.364) (j) or EV weight (tā=ā1.109, Pā=ā0.255) (k). Two-sided independent-sample t test without correction was used for all significance testing in iāk.