Cervical cancer
Conditions
Interventions
Observation group:None
Sponsors
The Affiliated Hospital of Southwest Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1.Referring to the guidelines of the National Comprehensive Cancer Network (NCCN) of the United States, patients diagnosed with cervical cancer were diagnosed with clinical symptoms and pathological examinations; 2.Patients > age 18 years; 3.The International Federation of Obstetrics and Gynecology (FIGO) stage is stage I.B3-IV.A, and patients who undergo concurrent chemoradiotherapy for the first time; 4.Informed consent and voluntary participation in this study; 5.Able to complete the scale independently or with the assistance of others; 6.The KPS score>= 70 points;
Exclusion criteria
Exclusion criteria: 1.Severe heart, brain, liver and kidney diseases and malignant tumors in other parts; 2.Those with mental disorders or language communication disorders; 3.Patients who have undergone major surgery to remove cervical cancer within 6 months prior to the start of the study; 4.Tumor recurrence.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Symptoms at different time points in patients with concurrent chemoradiotherapy for cervical cancer (symptom incidence and severity, severity of symptom interference);The number of symptom clusters, the composition of symptoms within clusters and their longitudinal trajectories; | — |
Countries
China
Contacts
Public ContactLi Li
The Affiliated Hospital of Southwest Medical University
Outcome results
None listed