104
Participants
Start Date
November 30, 2004
Primary Completion Date
December 31, 2009
Study Completion Date
June 30, 2010
Routine Data collection
"Patients assigned to the control arm answered PediQUEST (PQ) surveys at most once a week and at least once a month. PQ-surveys were administered through a tablet computer if patient was at the clinic or ward or over the phone if patient was primarily at home. PQ-survey had 9 age- and respondent- adapted versions.~Control arm participants reported their satisfaction with the PediQUEST technology twice 4th and 8th PediQUEST administration. These surveys were embedded in PediQUEST."
Feedback of patient-reported outcomes
Patients, parents and primary providers received printed reports summarizing patient/parent reported outcomes for last five visits. When child reported moderate-severe distress an email was automatically sent to primary providers (oncologist, nurses and psychosocial clinicians), as well as to the pain and palliative care services.
Children's Hospital of Philapdelphia, Philadelphia
Seattle Children's Hospital, Seattle
Boston Children's Hospital, Boston
Dana Farber Cancer Institute, Boston
National Cancer Institute (NCI)
NIH
Dana-Farber Cancer Institute
OTHER