Virtual Multimodal Support Program to Reduce Complications After Colorectal Cancer Surgery A Randomized Trial Comparing Virtual Hub Intervention with Usual Care

What this Trial Is About

Researchers are evaluating the effectiveness of a personalized stepped, multidisciplinary intervention delivered through a virtual multimodal rehabilitation hub for adults undergoing colorectal cancer surgery. The main goal is to reduce postoperative complications within 30 days after surgery compared to usual care. The study also aims to assess differences in quality of life, days spent at home after surgery, quality of recovery, cost-effectiveness, and implementation metrics over time. Participants will be randomly assigned to either the intervention group, which receives usual care plus tailored exercise, nutritional, psychological, nursing support, and group peer support delivered virtually before and after surgery, or the control group, which receives usual care alone. The interventions frequency and duration are adjusted based on individual needs and can last up to 12 months post-surgery. If needed, participants will be provided with devices and internet access to engage in virtual sessions. During the study, participants will be screened and consented before surgery, undergo baseline assessments, and be monitored regularly using standardized tools to evaluate recovery, quality of life, and days at home up to one year after surgery. Safety and data quality will be overseen by an independent monitoring board. The total study duration is approximately five years, and patient-reported outcomes will be carefully documented throughout.

PRIORITY-CONNECT 2 Trial