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The Higher the score the better quality of life.","dispersionType":"Standard Deviation","groups":[{"description":"Ann Arbor stage IIB, IIIB, IVA, or IVB risk participants received 2 cycles of AEPE/CAPDac chemotherapy and reported symptoms distress scale (SDS).","id":"OG000","title":"AEPA/CAPDac"},{"description":"Ann Arbor stage IIB, IIIB, or any IV risk participants received 12 weeks Stanford V Chemotherapy","id":"OG001","title":"HOD99 Unfavorable Risk 2 Arm (UR2)"}],"paramType":"MEAN","populationDescription":"Each institution made the decision whether to complete the QoL objective. Participation in the Quality of Life part of the trial is voluntary for participating institutions and voluntary by patient.","reportingStatus":"POSTED","timeFrame":"At Diagnosis (baseline) (T1), completion of 2 cycles of chemotherapy (approximately 2 months) (T2), completion of 4 cycles of chemotherapy (approximately 4 months) (T3), completion of radiation (approximately 8 months) (T4)","title":"To Assess the Patient Reported Symptoms and Health-related Quality of Life in Children With High Risk HL Compared to Those Treated on the Unfavorable HOD99 Treatment Arm (UR2) at Multiple Time Points. (PedsQL v.4.0)","type":"SECONDARY","unitOfMeasure":"score on a scale"}