Symptom distress in colorectal cancer during chemotherapy
Conditions
Interventions
Intervention Group:Symptom management guidance based on salutogenesis model + routine care
Sponsors
Affiliated Hospital of Jiangnan University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.Age >= 18 years old,; 2.Patients with colorectal cancer with a pathologically confirmed diagnosis and no metastasis or spread,; 3.Patients receiving at least 1 chemotherapy treatment with 6 or more cycles of chemotherapy (21 days for 1 cycle of chemotherapy),; 4.Karnofsky Performance Status score = 60 points, and understand their condition,; 5.Conscious, unimpaired reading, comprehension and communication skills,; 6.Voluntarily participate in this study and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1.Patients with a combination of other malignant tumors or end-stage disease,; 2.Patients with combined cognitive dysfunction or mental disorders,; 3.Patients with heart, liver, lung, renal or other serious complications,; 4.Patients who have previously participated in a similar intervention or are participating in another intervention study,; 5.Patients who are deemed by the investigator to be otherwise unsuitable for participation in the intervention study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Symptom distress;Sense of coherence; | — |
Secondary
| Measure | Time frame |
|---|---|
| Physical functioning;Anxiety and depression;Quality iof life;Self-efficacy;Coping styles; | — |
Countries
China
Contacts
Public ContactDanfeng Gu
Affiliated Hospital of Jiangnan University
Outcome results
None listed