000166564 001__ 166564
000166564 005__ 20240229123231.0
000166564 0247_ $$2doi$$a10.2196/21693
000166564 0247_ $$2pmid$$apmid:33295291
000166564 037__ $$aDKFZ-2020-03007
000166564 041__ $$aeng
000166564 082__ $$a610
000166564 1001_ $$00000-0003-1292-1352$$aSprave, Tanja$$b0
000166564 245__ $$aApp-Controlled Treatment Monitoring and Support for Head and Neck Cancer Patients (APCOT): Protocol for a Prospective Randomized Controlled Trial.
000166564 260__ $$aToronto$$c2020
000166564 3367_ $$2DRIVER$$aarticle
000166564 3367_ $$2DataCite$$aOutput Types/Journal article
000166564 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1675086644_25376
000166564 3367_ $$2BibTeX$$aARTICLE
000166564 3367_ $$2ORCID$$aJOURNAL_ARTICLE
000166564 3367_ $$00$$2EndNote$$aJournal Article
000166564 520__ $$aHead and neck cancers (HNCs) are among the most common malignancies, which often require multimodal treatment that includes radiation therapy and chemotherapy. Patients with HNC have a high burden of symptoms due to both the damaging effects of the tumor and the aggressive multimodal treatment. Close symptom monitoring over the course of the disease may help to identify patients in need of medical interventions.This APCOT (App-Controlled Treatment Monitoring and Support for Head and Neck Cancer Patients) trial is designed to assess the feasibility of monitoring HNC patients during the course of (chemo)radiation therapy daily using a mobile app. Additionally, symptom patterns, patient satisfaction, and quality of life will be measured in app-monitored patients in comparison to a patient cohort receiving standard-of-care physician appointments, and health economy aspects of app monitoring will be analyzed.This prospective randomized single-center trial will evaluate the feasibility of integrating electronic patient-reported outcome measures (ePROMs) into the treatment workflow of HNC patients. Patients undergoing definitive or adjuvant (chemo)radiation therapy as part of their HNC treatment at the Department of Radiation Oncology, University Medical Center Freiburg (Freiburg, Germany) will receive weekly physician appointments and additional appointments as requested to monitor and potentially treat symptoms during the course of treatment. Patients in the experimental arm will additionally be monitored daily using a dedicated app regarding their disease- and treatment-related symptoms, quality of life, and need for personal physician appointments. The feasibility of ePROM monitoring will be tested as the primary endpoint and will be defined if ≥80% of enrolled patients have answered ≥80% of their daily app-based questions. Quality of life will be assessed using the validated European Organisation for Research and Treatment of Cancer questionnaires, and patient satisfaction will be measured by the validated Patient Satisfaction Questionnaire Short Form at the initiation, in the middle, and at completion of radiation therapy, as well as at follow-up examinations. Additionally, the number and duration of physician appointments during the course of radiation therapy will be quantified for both ePROM-monitored and standard-of-care patients.This trial will enroll 100 patients who will be randomized (1:1) between the experimental arm with ePROM monitoring and the control arm with standard patient care. Recruitment will take 18 months, and trial completion is planned at 24 months after enrollment of the last patient.This trial will establish the feasibility of close ePROM monitoring of HNC patients undergoing (chemo)radiation therapy. The results can form the basis for further trials investigating potential clinical benefits of detailed symptom monitoring and patient-centered care in HNC patients regarding oncologic outcomes and quality of life.German Clinical Trials Register DRKS00020491; https://www.drks.de/drks_web/navigate.do?navigationId=trial.HTML&TRIAL_ID=DRKS00020491.PRR1-10.2196/21693.
000166564 536__ $$0G:(DE-HGF)POF3-315$$a315 - Imaging and radiooncology (POF3-315)$$cPOF3-315$$fPOF III$$x0
000166564 588__ $$aDataset connected to CrossRef, PubMed,
000166564 650_7 $$2Other$$aHNSCC
000166564 650_7 $$2Other$$ahead and neck cancer
000166564 650_7 $$2Other$$amHealth
000166564 650_7 $$2Other$$amobile app
000166564 650_7 $$2Other$$apatient-reported outcome measures
000166564 650_7 $$2Other$$aquality of life
000166564 650_7 $$2Other$$aradiotherapy
000166564 7001_ $$00000-0001-9929-7403$$aZöller, Daniela$$b1
000166564 7001_ $$0P:(DE-He78)75b4c256a6de824414938cf2aaeff88e$$aStoian, Raluca$$b2
000166564 7001_ $$0P:(DE-HGF)0$$aRühle, Alexander$$b3
000166564 7001_ $$00000-0001-8695-0194$$aKalckreuth, Tobias$$b4
000166564 7001_ $$00000-0002-2222-7324$$aHaehl, Erik$$b5
000166564 7001_ $$00000-0002-7869-9136$$aFahrner, Harald$$b6
000166564 7001_ $$00000-0002-5666-8662$$aBinder, Harald$$b7
000166564 7001_ $$00000-0003-2255-2255$$aGrosu, Anca-Ligia$$b8
000166564 7001_ $$00000-0002-7282-8689$$aHeinemann, Felix$$b9
000166564 7001_ $$0P:(DE-HGF)0$$aNicolay, Nils Henrik$$b10$$eLast author
000166564 773__ $$0PERI:(DE-600)2719222-2$$a10.2196/21693$$gVol. 9, no. 12, p. e21693 -$$n12$$pe21693$$tJMIR Research Protocols$$v9$$x1929-0748$$y2020
000166564 909CO $$ooai:inrepo02.dkfz.de:166564$$pVDB
000166564 9101_ $$0I:(DE-588b)2036810-0$$60000-0003-1292-1352$$aDeutsches Krebsforschungszentrum$$b0$$kDKFZ
000166564 9101_ $$0I:(DE-588b)2036810-0$$6P:(DE-He78)75b4c256a6de824414938cf2aaeff88e$$aDeutsches Krebsforschungszentrum$$b2$$kDKFZ
000166564 9101_ $$0I:(DE-588b)2036810-0$$6P:(DE-HGF)0$$aDeutsches Krebsforschungszentrum$$b3$$kDKFZ
000166564 9101_ $$0I:(DE-588b)2036810-0$$60000-0001-8695-0194$$aDeutsches Krebsforschungszentrum$$b4$$kDKFZ
000166564 9101_ $$0I:(DE-588b)2036810-0$$60000-0002-2222-7324$$aDeutsches Krebsforschungszentrum$$b5$$kDKFZ
000166564 9101_ $$0I:(DE-588b)2036810-0$$60000-0003-2255-2255$$aDeutsches Krebsforschungszentrum$$b8$$kDKFZ
000166564 9101_ $$0I:(DE-588b)2036810-0$$60000-0002-7282-8689$$aDeutsches Krebsforschungszentrum$$b9$$kDKFZ
000166564 9101_ $$0I:(DE-588b)2036810-0$$6P:(DE-HGF)0$$aDeutsches Krebsforschungszentrum$$b10$$kDKFZ
000166564 9131_ $$0G:(DE-HGF)POF3-315$$1G:(DE-HGF)POF3-310$$2G:(DE-HGF)POF3-300$$3G:(DE-HGF)POF3$$4G:(DE-HGF)POF$$aDE-HGF$$bGesundheit$$lKrebsforschung$$vImaging and radiooncology$$x0
000166564 9141_ $$y2020
000166564 915__ $$0StatID:(DE-HGF)0300$$2StatID$$aDBCoverage$$bMedline$$d2020-09-02
000166564 915__ $$0StatID:(DE-HGF)0320$$2StatID$$aDBCoverage$$bPubMed Central$$d2020-09-02
000166564 915__ $$0StatID:(DE-HGF)0501$$2StatID$$aDBCoverage$$bDOAJ Seal$$d2020-09-02
000166564 915__ $$0StatID:(DE-HGF)0500$$2StatID$$aDBCoverage$$bDOAJ$$d2020-09-02
000166564 915__ $$0StatID:(DE-HGF)0030$$2StatID$$aPeer Review$$bDOAJ : Peer review$$d2020-09-02
000166564 915__ $$0LIC:(DE-HGF)CCBYNV$$2V:(DE-HGF)$$aCreative Commons Attribution CC BY (No Version)$$bDOAJ$$d2020-09-02
000166564 915__ $$0StatID:(DE-HGF)0199$$2StatID$$aDBCoverage$$bClarivate Analytics Master Journal List$$d2020-09-02
000166564 915__ $$0StatID:(DE-HGF)0112$$2StatID$$aWoS$$bEmerging Sources Citation Index$$d2020-09-02
000166564 915__ $$0StatID:(DE-HGF)0150$$2StatID$$aDBCoverage$$bWeb of Science Core Collection$$d2020-09-02
000166564 915__ $$0StatID:(DE-HGF)0561$$2StatID$$aArticle Processing Charges$$d2020-09-02
000166564 915__ $$0StatID:(DE-HGF)0700$$2StatID$$aFees$$d2020-09-02
000166564 9201_ $$0I:(DE-He78)FR01-20160331$$kFR01$$lDKTK FR zentral$$x0
000166564 9201_ $$0I:(DE-He78)E055-20160331$$kE055$$lE055 KKE Molekulare Radioonkologie$$x1
000166564 980__ $$ajournal
000166564 980__ $$aVDB
000166564 980__ $$aI:(DE-He78)FR01-20160331
000166564 980__ $$aI:(DE-He78)E055-20160331
000166564 980__ $$aUNRESTRICTED