{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","value":"18"}],"title":"Requested to be removed from study"},{"measurements":[{"groupId":"OG000","value":"3"}],"title":"Did not undergo lapartomy"},{"measurements":[{"groupId":"OG000","value":"2"}],"title":"Incompatible internet browser"},{"measurements":[{"groupId":"OG000","value":"1"}],"title":"Died"},{"measurements":[{"groupId":"OG000","value":"69"}],"title":"Completed preoperative session in STAR"},{"measurements":[{"groupId":"OG000","value":"27"}],"title":"Didn't complete preop, completed other surveys"}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"120"}],"units":"Participants"}],"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":"COUNT_OF_PARTICIPANTS","reportingStatus":"POSTED","timeFrame":"once pre-operatively and then weekly starting 7 days after surgery until the 6-week post-operative period has ended.","title":"Feasibility of Electronic Capture of Patient-reported Symptoms From Home Following Major Gynecologic Cancer Surgery","type":"PRIMARY","unitOfMeasure":"Participants"}