Nasopharyngeal carcinoma
Conditions
Interventions
Experimental group:Usual care+Light therapy (500Lux, 500nm green enriched blue)
Control group:Usual care+Blank control (phototherapy equipment is off)
Sponsors
Cancer Hospital Affiliated to Guangxi Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Patients with newly diagnosed nasopharyngeal carcinoma confirmed by pathology; 2. Patients who meet the ICD-10 fatigue diagnostic criteria; 3. Patients who received three-dimensional IMRT; 4. The patients who were treated with induction chemotherapy and radiotherapy combined with concurrent chemotherapy were treated with conventional dose of 2gy /time a day, 5 times a week, the total dose was 60-66gy, and the radiotherapy time was 6 weeks; 5. Patients older than 18 years old or above; 6. Patients and their family members voluntarily participated in the survey with informed consent.
Exclusion criteria
Exclusion criteria: 1. Patients with cognitive impairment, consciousness disorder or long-term use of antipsychotics; 2. Patients with other tumors or distant metastasis; 3. Patients with other serious physical diseases; 4. Patients with eye diseases or eye diseases; 5. Patients who stopped treatment; 6. Patients who drop out or lose follow-up.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cancer Related Fatigue; | — |
Secondary
| Measure | Time frame |
|---|---|
| Anxiety and Depression;The quality of life; | — |
Countries
China
Contacts
Public ContactJiang JinFang
Cancer Hospital Affiliated to Guangxi Medical University
Outcome results
None listed