{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","lowerLimit":"7.14","upperLimit":"92.86","value":"75"},{"groupId":"OG001","lowerLimit":"7.14","upperLimit":"92.86","value":"60.7"},{"groupId":"OG002","lowerLimit":"7.14","upperLimit":"92.85","value":"71.4"}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"213"},{"groupId":"OG001","value":"24"},{"groupId":"OG002","value":"123"}],"units":"Participants"}],"title":"Global Health"},{"categories":[{"measurements":[{"groupId":"OG000","lowerLimit":"5","upperLimit":"76.67","value":"58.3"},{"groupId":"OG001","lowerLimit":"13.3","upperLimit":"76.67","value":"58.3"},{"groupId":"OG002","lowerLimit":"21.67","upperLimit":"76.67","value":"65"}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"205"},{"groupId":"OG001","value":"23"},{"groupId":"OG002","value":"122"}],"units":"Participants"}],"title":"Functional Scale"},{"categories":[{"measurements":[{"groupId":"OG000","lowerLimit":"23.1","upperLimit":"92.3","value":"44.2"},{"groupId":"OG001","lowerLimit":"26.9","upperLimit":"90.38","value":"43.3"},{"groupId":"OG002","lowerLimit":"23.1","upperLimit":"86.53","value":"34.6"}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"209"},{"groupId":"OG001","value":"24"},{"groupId":"OG002","value":"123"}],"units":"Participants"}],"title":"Symptom Scale"}],"denoms":[{"counts":[{"groupId":"OG000","value":"213"},{"groupId":"OG001","value":"24"},{"groupId":"OG002","value":"123"}],"units":"Participants"}],"description":"EORTC QLQ-C30 subscale and overall scores will be used to describe participant symptom and health-related quality of life burden. Baseline EORTC QLQ-C30 scores will be compared according to cancer group. The EORTC QLQ-C30 is a 30-item core cancer specific questionnaire measuring QOL in cancer patients. It incorporates five functional scales (physical, role, cognitive, emotional, and social), three symptom scales (fatigue, pain, and nausea and vomiting), a global health status / QoL scale, and single items assessing additional symptoms and perceived financial impact of the disease. Most questions use a 4-point scale (1 'Not at All' to 4 'Very Much'); 2 questions use a 7-point scale (1 'Very Poor' to 7 'Excellent'). Scores are averaged, and transformed to 0-100 scale; higher score=higher response level.","dispersionType":"Full Range","groups":[{"description":"Considering or currently receiving cancer treatment\n\nNon-Interventional: Participants will be identified via screening of electronic medical records or institutional databases. All eligible participants will have one visit for the collection of broad demographic and clinical data. Data collection at study visit will occur via survey procedures and/or medical record review.\n\nNon-Interventional Follow-up: Participants initiating or receiving ongoing treatment for their cancer will attend a single follow-up visit to recollect broad demographic and clinical data. Data collection at study visits will occur via survey procedures and/or medical record review.","id":"OG000","title":"New, Primary or Recurrent Disease"},{"description":"This includes cases for which there are no current definitive therapy options for cure (i.e., inoperable) but may be considered for non-standard / non-curative therapies.\n\nNon-Interventional: Participants will be identified via screening of electronic medical records or institutional databases. All eligible participants will have one visit for the collection of broad demographic and clinical data. Data collection at study visit will occur via survey procedures and/or medical record review.\n\nNon-Interventional Follow-up: Participants initiating or receiving ongoing treatment for their cancer will attend a single follow-up visit to recollect broad demographic and clinical data. Data collection at study visits will occur via survey procedures and/or medical record review.","id":"OG001","title":"Metastic or Locally Advanced Cancer"},{"description":"Prior diagnosis (within 5 years), in remission - Not currently on cancer treatment other than ART or maintenance therapy.\n\nNon-Interventional: Participants will be identified via screening of electronic medical records or institutional databases. All eligible participants will have one visit for the collection of broad demographic and clinical data. Data collection at study visit will occur via survey procedures and/or medical record review.","id":"OG002","title":"Prior Cancer"}],"paramType":"MEDIAN","populationDescription":"Participants who enrolled in this study with EORTC QLQ-C30 information","reportingStatus":"POSTED","timeFrame":"Baseline","title":"Describe the Health-related QOL of Cancer Patients With HIV at Domestic AMC Sites Using European Organization for Research and Treatment of Cancer Quality of Life Questionnaire [EORTC QLQ-C30]","type":"OTHER_PRE_SPECIFIED","unitOfMeasure":"score on a scale between 0 and 100"}