About this trial
This is a prospective, single-center, exploratory study designed to evaluate the accuracy, user engagement, and user experience of the BaiXiaoAi Companion AI. Upon signing the informed consent form and enrollment, a dedicated "Doctor-Nurse-Patient-AI" WeChat group will be established for each participant. Within the group, the BaiXiaoAi AI will provide timely responses based on patient communications and proactively push information regarding disease management and patient education.
Eligibility criteria
Qualifiers
Adults aged 18 years or older;
Patients with a confirmed diagnosis of malignant neoplasms who are currently undergoing treatment or in follow-up, or their primary caregivers;
Able to read and communicate in Chinese and independently use WeChat;
Willing and able to provide informed consent.
Disqualifiers
Presence of severe psychiatric disorders (e.g., schizophrenia, bipolar disorder) or cognitive impairment (MMSE score < 24);
Inability to use WeChat or communicate in Chinese;
Considered by the investigators to be unsuitable for participation due to psychological or physical conditions.
Trial design
Treatments tested in this trial
- No Intervention: Observational Cohort