BackgroundDecision‐making after local resection of T1 colorectal cancer (T1CRC) is often complex and calls for optimal information provision as well as active patient involvement.ObjectiveThe aim was to evaluate the perceptions of patients with T1CRC on information provision and therapeutic decision‐making.MethodsThis multicenter cross‐sectional study included patients who underwent endoscopic or local surgical resection as initial treatment. Information provision was assessed using the EORTC QLQ‐INFO25 questionnaire. In patients with high‐risk T1CRC, we evaluated decisional involvement and satisfaction regarding the choice as to whether to undergo additional treatment after local resection, and the level of decisional conflict using the Decisional Conflict Scale.ResultsNinety‐eight patients with T1CRC were included (72% response rate; 79/98 endoscopic and 19/98 local surgical resection; 45/98 high‐risk T1CRC). Median time since local resection was 28 months (IQR 18); none had developed recurrence. Unmet information needs were reported by 29 patients (30%; 18 low‐risk, 11 high‐risk), mostly on post‐treatment related topics (follow‐up visits, recovery time, recurrence prevention). After local resection, 24 of the 45 high‐risk patients (53%) underwent additional treatment, while others were subjected to surveillance. Higher‐educated patients were more often actively involved in decision‐making (93% vs. 43%, p = 0.002) and more frequently underwent additional treatment (79% vs. 40%, p = 0.02). Decisional conflict (p = 0.19) and satisfaction (p = 0.78) were comparable between higher‐ and lower‐educated high‐risk patients.ConclusionGreater attention should be given to the post‐treatment course during consultations following local T1CRC resection. The differences in decisional involvement and selected management strategies between higher‐ and lower‐educated high‐risk patients warrant further investigation.