nasopharynx cancer
Conditions
Interventions
intervention group:After completing the preliminary exercise risk screening, the research team discussed and formed an individualized exercise plan with the patients according to the corresponding key
control group:The control group was guided by routine exercise prescription, and the responsible nurse guided the exercise according to the patient's feedback and own experience, and distributed the e
Sponsors
The First Affiliated Hospital of Fujian Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: The inclusion criteria of the retrospective cohort study in the protocol construction phase were: ? The patient with stage I-IVa non-keratic nasopharyngeal carcinoma (the 8th edition of nasopharyngeal carcinoma in 2018 UICC/AJCC staging criteria) were first diagnosed by histopathological examination;? Aged =18 years, patients were aware of their diagnosis and condition;? Receive radiotherapy alone; Intensity modulated conformal radiotherapy + concurrent chemotherapy; Induction chemotherapy + intensity-modulated radiotherapy + concurrent chemotherapy; ?Have certain reading and comprehension ability, no hearing impairment;? Volunteer to join the study and sign the informed consent. The inclusion criteria for the programme implementation phase are ibid.
Exclusion criteria
Exclusion criteria: The exclusion criteria of retrospective cohort study in protocol construction stage were: (1) discontinuation of radiotherapy; ? Patients with cognitive and mental illness or serious disability problems; ? Blood clots occur during the treatment, etc. The exclusion criteria in the implementation phase of the program are: ? those who have cognitive or mental disorders or physical dysfunction can not cooperate; ? Patients with other malignant tumors or bone metastases; ? There are serious heart and brain, lung, blood vessel, liver and kidney function diseases, such as heart disease, stroke, pulmonary insufficiency, thrombosis, etc.; ? The doctor in charge considered it inappropriate to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| cancer-related fatigure; | — |
Secondary
| Measure | Time frame |
|---|---|
| Exercise compliance rate;nutritional status;quality of life;anxiety and depression ;social support;body composition; | — |
Countries
China
Contacts
Public ContactJinsheng Hong
The First Affiliated Hospital of Fujian Medical University
Outcome results
None listed