{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","value":"15"}]}],"title":"ECOG Performance Status"},{"categories":[{"measurements":[{"groupId":"OG000","value":"14"}]}],"title":"Nausea"},{"categories":[{"measurements":[{"groupId":"OG000","value":"12"}]}],"title":"Fatigue"},{"categories":[{"measurements":[{"groupId":"OG000","value":"17"}]}],"title":"Trouble with Strenuos Activities"},{"categories":[{"measurements":[{"groupId":"OG000","value":"11"}]}],"title":"Constipation"},{"categories":[{"measurements":[{"groupId":"OG000","value":"11"}]}],"title":"Pain"}],"denoms":[{"counts":[{"groupId":"OG000","value":"120"}],"units":"Participants"}],"description":"The percentage of symptoms generated by patients on protocol","groups":[{"description":"This study will assess patient use of WEBCORE, an online system designed for cancer patients to self-record toxicity-related symptoms based on NCI Common Terminology Criteria for Adverse Events and global quality of life (QoL) by European Organization for Research and Treatment of Cancer (EORTC QLQ-C30).\n\nonline platform WEBCORE: Enrollees will be sent weekly email reminders to login to WEBCORE from home. Participants will be expected to complete the questionnaire once pre-operatively and then weekly starting 7 days after surgery until the 6-week post-operative period has ended.","id":"OG000","title":"GYN Pts Undergoing Surgery"}],"paramType":"NUMBER","reportingStatus":"POSTED","timeFrame":"weekly starting 7 days after surgery until the 6-week post-operative period","title":"Most Commonly Reported and Most Distressing Symptoms Reported by Patients After Gynecologic Cancer Surgery Using the STAR System","type":"SECONDARY","unitOfMeasure":"percentage of symptoms"}