AUTHOR=Cavalieri Stefano , Vener Claudia , LeBlanc Marissa , Lopez-Perez Laura , Fico Giuseppe , Resteghini Carlo , Monzani Dario , Marton Giulia , Pravettoni Gabriella , Moreira-Soares Mauricio , Filippidou Despina Elizabeth , Almeida Aitor , Bilbao Aritz , Mehanna Hisham , Singer Susanne , Thomas Steve , Lacerenza Luca , Manfuso Alfonso , Copelli Chiara , Mercalli Franco , Frigessi Arnoldo , Martinelli Elena , Licitra Lisa , BD4QoL Consortium , Fossen Erlend I. F. , Taylor Katherine , Nankivell Paul , De Mriganke , Abou-Foul Ahmad , Estevez-Priego Estefania , Cabrera-Umpierrez Maria Fernanda , Alonso Itziar , Copelli Sergio , Ness Andy , Pring Miranda , Hurley Katrina TITLE=A multicenter randomized trial for quality of life evaluation by non-invasive intelligent tools during post-curative treatment follow-up for head and neck cancer: Clinical study protocol JOURNAL=Frontiers in Oncology VOLUME=13 YEAR=2023 URL=https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2023.1048593 DOI=10.3389/fonc.2023.1048593 ISSN=2234-943X ABSTRACT=

Patients surviving head and neck cancer (HNC) suffer from high physical, psychological, and socioeconomic burdens. Achieving cancer-free survival with an optimal quality of life (QoL) is the primary goal for HNC patient management. So, maintaining lifelong surveillance is critical. An ambitious goal would be to carry this out through the advanced analysis of environmental, emotional, and behavioral data unobtrusively collected from mobile devices. The aim of this clinical trial is to reduce, with non-invasive tools (i.e., patients’ mobile devices), the proportion of HNC survivors (i.e., having completed their curative treatment from 3 months to 10 years) experiencing a clinically relevant reduction in QoL during follow-up. The Big Data for Quality of Life (BD4QoL) study is an international, multicenter, randomized (2:1), open-label trial. The primary endpoint is a clinically relevant global health-related EORTC QLQ-C30 QoL deterioration (decrease ≥10 points) at any point during 24 months post-treatment follow-up. The target sample size is 420 patients. Patients will be randomized to be followed up using the BD4QoL platform or per standard clinical practice. The BD4QoL platform includes a set of services to allow patients monitoring and empowerment through two main tools: a mobile application installed on participants’ smartphones, that includes a chatbot for e-coaching, and the Point of Care dashboard, to let the investigators manage patients data. In both arms, participants will be asked to complete QoL questionnaires at study entry and once every 6 months, and will undergo post-treatment follow up as per clinical practice. Patients randomized to the intervention arm (n=280) will receive access to the BD4QoL platform, those in the control arm (n=140) will not. Eligibility criteria include completing curative treatments for non-metastatic HNC and the use of an Android-based smartphone. Patients undergoing active treatments or with synchronous cancers are excluded.

Clinical Trial Registration: ClinicalTrials.gov, identifier (NCT05315570).