About this trial
This study is a researcher-initiated, multi-center, prospective, two-arm interventional randomized controlled study across the country. It aims to explore whether an Internet of Things-based RIS system can enhance the medical experience of patients with radiation-induced oropharyngeal mucositis during the diagnosis and treatment process among head and neck cancer patients undergoing radiotherapy.
Eligibility criteria
Qualifiers
Voluntarily sign the informed consent form;
Reached the age of 18 on the date of signing the informed consent form, and under the age of 65;
Patients diagnosed with head and neck tumors and receiving radiotherapy as per the 2017 WHO standards and guidelines.
According to the doctor's assessment, patients may experience radiation-induced oropharyngeal mucositis during radiotherapy.
Disqualifiers
Have other uncontrolled serious diseases, such as unstable heart diseases requiring treatment, poorly controlled diabetes (fasting blood sugar > 1.5 times the upper limit of the normal value), mental disorders, and a severe history of allergies.
Trial design
Treatments tested in this trial
- RIS system