Cancer of digestive system, urinary system, endocrine system, breast system and respiratory system.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Diagnosed by pathological biopsy or imaging examination as digestive system cancer, urinary system cancer, endocrine cancer, breast cancer and respiratory system cancer, which meet the diagnostic criteria of clinical diagnosis and treatment guidelines for corresponding cancer types. 2. The stages of treatment are clear, which meet the following definitions: (1) Preoperative group: patients who have not received core treatment such as surgery and chemotherapy after diagnosis are planned to undergo surgery, with no surgical contraindications and stable condition; (2) Postoperative group: 1-3 months after the surgical treatment, the wound healed well, without serious complications such as postoperative infection and bleeding, and did not enter the rehabilitation stage, and did not enter the synchronous stage of radiotherapy and chemotherapy; (3) Chemotherapy stage group: receiving systemic chemotherapy (cycle 1-6), non-chemotherapy acute stage (except within 1 week after chemotherapy), bone marrow suppression =18 years old, regardless of gender, clear consciousness, and normal communication and understanding of research contents. 4. The visual acuity is normal or normal after correction (corrected visual acuity >=0.8), and no eye diseases (cataract, glaucoma, etc.) affect eye movement data collection. 5. Volunteer to participate in this study and sign a written informed consent form.
Exclusion criteria
Exclusion criteria: 1. There is cognitive disorder, mental illness or communication disorder, and it is impossible to cooperate with eye movement test, questionnaire filling and interview. 2. Eye diseases, nervous system diseases (such as Parkinson's disease) or taking drugs that affect eye movements (such as anticholinergic drugs) may interfere with eye movement data. 3, the condition is unstable: patients with chemotherapy stage have ?-? bone marrow suppression and severe nausea and vomiting; Postoperative wound infection/bleeding was not controlled; The disease progressed during the rehabilitation period; Preoperative patients with severe basic diseases can not tolerate the test. 4. Being allergic or strongly resistant to the health information materials used in the research. 5. Have participated in similar health information preference research in the past 3 months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Gaze duration;Gaze trajectory;Region of interest;Number of fixation points;Focus on hot spots; | — |
Secondary
| Measure | Time frame |
|---|---|
| Pupil diameter variation;Saccade frequency; | — |
Countries
China
Contacts
Shanghai Tenth People's hospital