Mean set loss errors across AST stages, mirroring error analysis in the Wisconsin Card Sorting Test (i.e. after 50% or more of the criterion of six consecutive responses has been achieved). EE paradoxically increased set-loss errors on R1 in Sham+VEH+EE rats compared to all other Sham groups (bp<0.01), although trials to criterion and total errors were similar among all control groups (Figs. 3 and 4). More set loss errors were made by the TBI+STD+VEH on the ED stage as compared to Sham+VEH+EE (ap<0.05), Sham+CIT+STD, and Sham+CIT+EE (both bp<0.01), but not Sham+VEH+STD. CIT and EE reduced set-loss errors in TBI rats (cp<0.05) when given individually, while the combined treatment led to a more pronounced reduction compared to TBI+VEH+STD rats (ep<0.001). On the R3 stage, TBI+VEH+STD rats displayed more set loss errors than Sham+VEH+STD rats (bp<0.01). Additionally, CIT and EE alone reduced set-loss errors in TBI rats (dp<0.01), while the combined paradigm rendered injured rats to complete the stage without set-loss errors, thus providing significant improvements compared to TBI+VEH+STD (ep<0.001) and TBI+VEH+EE (fp<0.05) groups.