{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","spread":"1.2","value":"-0.3"},{"groupId":"OG001","spread":"1.1","value":"-0.3"}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"19"},{"groupId":"OG001","value":"27"}],"units":"Participants"}],"title":"Pain"},{"categories":[{"measurements":[{"groupId":"OG000","spread":"0.9","value":"-0.1"},{"groupId":"OG001","spread":"1.2","value":"0.4"}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"20"},{"groupId":"OG001","value":"27"}],"units":"Participants"}],"title":"Fatigue"},{"categories":[{"measurements":[{"groupId":"OG000","spread":"0.7","value":"-0.3"},{"groupId":"OG001","spread":"1.0","value":"0.3"}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"19"},{"groupId":"OG001","value":"27"}],"units":"Participants"}],"title":"Nausea"},{"categories":[{"measurements":[{"groupId":"OG000","spread":"1.0","value":"-0.1"},{"groupId":"OG001","spread":"0.9","value":"-0.1"}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"19"},{"groupId":"OG001","value":"27"}],"units":"Participants"}],"title":"Anxiety"}],"denoms":[{"counts":[{"groupId":"OG000","value":"20"},{"groupId":"OG001","value":"27"}],"units":"Participants"}],"description":"Measured by patient-reported National Cancer Institute \\[NCI\\] Patient Reported Outcomes \\[PRO\\]-CTCAE. The change in severity from baseline to 3 months was calculated and it ranged from -3 to 3. The severity was measured on a 0-3 (0=None, 3=Severe) scale with a higher value representing a worse outcome and a lower value representing a better outcome. This was done separately for pain, fatigue, nausea, and anxiety.","dispersionType":"Standard Deviation","groups":[{"description":"Patients undergo acupuncture during chemotherapy infusion on day 1 and fluorouracil pump disconnect on day 3 of each biweekly chemotherapy infusion over 12 weeks. Patients also undergo self-administered acupressure over 11 minutes daily for 12 weeks and undergo standard of care oral cryotherapy.\n\nAcupuncture Therapy: Undergo acupuncture\n\nAcupressure Therapy: Undergo acupressure\n\nOral Cryotherapy: Undergo oral cryotherapy\n\nQuestionnaire Administration: Ancillary studies\n\nQuality-of-Life Assessment: Ancillary studies","id":"OG000","title":"Arm I (Acupuncture, Acupressure, Cryotherapy)"},{"description":"Patients undergo standard of care oral cryotherapy.\n\nOral Cryotherapy: Undergo oral cryotherapy\n\nQuestionnaire Administration: Ancillary studies\n\nQuality-of-Life Assessment: Ancillary studies","id":"OG001","title":"Arm II (Cryotherapy)"}],"paramType":"MEAN","populationDescription":"Due to missing patient reported outcomes the overall number of participants analyzed differs from patients that completed the study.","reportingStatus":"POSTED","timeFrame":"3 months","title":"Change in Severity of Pain, Fatigue, Nausea, and Anxiety From Baseline to 3 Months","type":"SECONDARY","unitOfMeasure":"units on a scale"}