Although patient-reported adverse events have been promoted as an essential element in clinical trials and daily managements, their efficacy remained unknown. The purpose of this trial was to determine the effect of the patient-reported adverse events during the treatment on the improvements on quality of life.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
320
The intervention was administrated through APP
patients receive normal care and visit
Sun Yat-sen University Cancer Center
Guangzhou, Guangdong, China
Score of physical functioning in quality of life
Score of physical functioning in quality of life
Time frame: within 1 week of study completion
3-year overall survival
overall survival at three year after diagnosis
Time frame: 3 year after diagnosis
3-year progression-free survival
progression-free survival at three year after diagnosis
Time frame: 3 year after diagnosis
3-year local-regional free survival
local-regional free survival at three year after diagnosis
Time frame: 3 year after diagnosis
3-year metastatic-free survival
metastatic-free survival at three year after diagnosis
Time frame: 3 year after diagnosis
completion rate
completion rate
Time frame: within 1 week of study completion
degrees of patients satisfaction regarding the treatment process
degrees of patients satisfaction regarding the treatment process
Time frame: within 1 week of study completion
response rate
response rate
Time frame: 1 month after study completion
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