{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","spread":"2.1","value":"2.8"}]}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"13"}],"units":"Participants"}],"description":"The Brief Pain Inventory - Short Form (BPI-SF) asks respondents to rate the severity of their current, least, average, and worst pain over the previous 24 hours on a scale of 0 to 10. The BPI-SF also asks respondents to rate on a scale of 0 to 10 the degree to which pain interfered with seven different areas of their life (e.g., general activity, normal work, etc.)Scale 0-10 with 0 being no pain and 10 being pain as bad as you can imagine.","dispersionType":"Standard Deviation","groups":[{"description":"The conjugate vaccine for Streptococcus pneumoniae will be administered during weeks 9, 17, and 25 after autologous HSCT - the study nurse will arrange for the vaccine to be administered at the specified time and the patient will be instructed to notify an investigator or study nurse of any side effects of vaccine administration. At the specified times, patients will fill out the quality-of-life assessment. All patients enrolled on this trial will have samples procured for all proposed laboratory correlative studies.\n\nStreptococcus pneumoniae: Patients will receive 0.5 mL Prevnar in the deltoid muscle during weeks 9, 17, and 25 after autologous hematopoietic stem cell transplantation (HSCT)\n\nlaboratory correlative studies: Approximately 30-mL of blood will be collected and sent to the appropriate research lab(s) for processing.\n\nquality-of-life assessment: Responses to Hospital Anxiety and Depression Scale, 9-item brief fatigue inventory 57, brief pain inventory, and the FACT-G.","id":"OG000","title":"Prevnar"}],"paramType":"MEAN","populationDescription":"Not all patients data was available due to incomplete surveys","reportingStatus":"POSTED","timeFrame":"Up to 3 years","title":"Quality of Life, Including Brief Pain Inventory","type":"SECONDARY","unitOfMeasure":"units on a scale"}