NCT03850912.

Study name	SIMPRO Research Center: Integration and Implementation of PROs for Symptom Management in Oncology Practice
Methods	Randomised parallel trial, USA
Participants	Adults aged >= 18 years, who meet one of the following: Suspected thoracic cancer [lung or bronchus] AND is inpatient following thoracic surgery. Suspected gastrointestinal cancer [colorectal, pancreas, liver/biliary, esophagus,or gastric] AND is inpatient following gastrointestinal surgery. Suspected gynecologic cancer [ovary, uterus, or cervix] AND is inpatient following gynecologic surgery. Diagnosis of thoracic cancer [lung or bronchus] AND scheduled to start a new treatment plan for thoracic cancer. Diagnosis of gastrointestinal cancer [colorectal, pancreas, liver/biliary, esophagus,or gastric] AND scheduled to start a new treatment plan for gastrointestinal cancer. Diagnosis of gynecologic cancer [ovary, uterus, or cervix] AND scheduled to start a new treatment plan for gynecologic cancer
Interventions	Intervention: participants will receive patient‐reported outcome measures and receive feedback Comparison: participants will receive patient‐reported outcome measures and not receive feedback
Outcomes	Main outcome: 'Emergency Department ‐ Treat and Release' (EDTR) Rate at 30‐days Other outcomes: symptom burden, patient satisfaction, initiation of adjuvant chemotherapy, sustainability of the intervention
Starting date	July 2019 (estimated completion date September 2023)
Contact information	Deborah Schrag
Notes