Impact of Patient-Reported Outcomes for Symptom Monitoring in Patients Followed for Head and Neck Squamous Cell Carcinoma (HNSCC)

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorCentre Henri Becquerel

About this trial

The use of digital strategies to systematically monitor patients' symptoms in clinical settings allows problems to be detected at an early stage before they worsen or lead to complications. In this study, the hypothesis is that the proportion of patients with a weight loss of at least 5% between before radiotherapy/radiochemotherapy and 3 months after treatment would be lower with optimised care thanks to remote monitoring using a medical telemonitoring solution in oncology.

Eligibility criteria

Qualifiers

Patient aged over 18 and under 75 years WHO score < 2,

Treated for localised heand and neck cancer of the squamous cell carcinoma type for which curative treatment has been chosen and receiving radiotherapy or radio-chemotherapy exclusively or as an adjuvant with the aim of cure

Having signed the informed consent form,

Affiliated with or beneficiary of a social protection scheme,

Disqualifiers

History of other neoplastic disease less than 2 years ago or progressive disease,

History of ENT radiotherapy,

Pregnant or breastfeeding women,

Protected adults (under guardianship, curatorship or judicial protection),

Trial design

Treatments tested in this trial

  • Remote symptoms moniotring

Treatment groups

192 Participants
are divided into 2 treatment groups

Sponsors and collaborators