Electronic toxicity monitoring and patient-reported outcomes.
about
Cognitive interviewing of the US National Cancer Institute's Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)Harnessing technology to improve clinical trials: study of real-time informatics to collect data, toxicities, image response assessments, and patient-reported outcomes in a phase II clinical trial.Computerized patient-reported symptom assessment in radiotherapy: a pilot randomized, controlled trial.The Value of Patient Reported Outcomes and Other Patient-Generated Health Data in Clinical Hematology.Comparison of seven-day and repeated 24-hour recall of symptoms in the first 100 days after hematopoietic cell transplantation.Linguistic validation of the Spanish version of the National Cancer Institute's Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE).The importance of symptom surveillance during follow-up care of leukemia, bladder, and colorectal cancer survivors.Cognitive Interview-Based Validation of the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events in Adolescents with Cancer.Feasibility of frequent patient-reported outcome surveillance in patients undergoing hematopoietic cell transplantation.Validity and Reliability of the US National Cancer Institute's Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)Longitudinal adverse event assessment in oncology clinical trials: the Toxicity over Time (ToxT) analysis of Alliance trials NCCTG N9741 and 979254Prognostic value of patient-reported symptom interference in patients with late-stage lung cancerThe first step to integrating the child's voice in adverse event reporting in oncology trials: a content validation study among pediatric oncology clinicians.Videotaping of surgical procedures and outcomes following extraperitoneal laparoscopic radical prostatectomy for clinically localized prostate cancer.Use of mobile device technology to continuously collect patient-reported symptoms during radiation therapy for head and neck cancer: A prospective feasibility studyPatient-Reported Physical Function Measures in Cancer Clinical Trials.The Imperative for a New Approach to Toxicity Analysis in Oncology Clinical Trials.The eSMART study protocol: a randomised controlled trial to evaluate electronic symptom management using the advanced symptom management system (ASyMS) remote technology for patients with cancer.Reducing the toxicity of cancer therapy: recognizing needs, taking action.
P2860
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P2860
Electronic toxicity monitoring and patient-reported outcomes.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on July 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Electronic toxicity monitoring and patient-reported outcomes.
@en
Electronic toxicity monitoring and patient-reported outcomes.
@nl
type
label
Electronic toxicity monitoring and patient-reported outcomes.
@en
Electronic toxicity monitoring and patient-reported outcomes.
@nl
prefLabel
Electronic toxicity monitoring and patient-reported outcomes.
@en
Electronic toxicity monitoring and patient-reported outcomes.
@nl
P2093
P2860
P1433
P1476
Electronic toxicity monitoring and patient-reported outcomes.
@en
P2093
Bryce B Reeve
Deborah Bruner
Emily Blauel
Ethan M Basch
Lauren Rogak
Lori Minasian
Paul Baumgartner
Ram Chilukuri
Sandra A Mitchell
P2860
P304
P356
10.1097/PPO.0B013E31822C28B3
P577
2011-07-01T00:00:00Z