colorectal cancer
Conditions
Interventions
Experimental Group of Colorectal Cancer Patients With Chemotherapy-Related Cognitive Impairment (Part III):The first draft of the chemotherapy-related cognitive impairment management protocol for colo
Sponsors
Fujian Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: Part 1: (1) Those who are receiving chemotherapy at least 1-2 times; (2) Age>= 18 years old; (3) Able to complete the required research questionnaire independently or with the help of the investigator;(4) Those who are informed of the diagnosis and agree to accept the study. Part 2: (1) Medical staff: (1) More than 5 years of work experience in oncology; (2) Intermediate and above titles; (3) Sign the informed consent form and voluntarily participate in this study. (2) Patients: (1) Patients who have been clearly diagnosed with colorectal cancer according to the diagnostic criteria for colorectal cancer and have received chemotherapy for 1-2 times; (2) Age>= 18 years old; (3) be able to understand the content of the interview; (4) Informed consent to participate in this study
Exclusion criteria
Exclusion criteria: (1) Those with tumor recurrence, brain metastasis or multiple metastases; (2) Patients with severe systemic infection, or other serious physical diseases, such as limb dysfunction, ascites, anemia, liver and kidney damage, infection, and heart disease; (3) Patients with neurological diseases and traumatic brain injury; (4) Those with a family history of hereditary mental illness; (5) Those who use drugs that have an effect on cognitive function; (6) Those who have been clearly diagnosed with cognitive impairment ;(7) Those who have severe visual, auditory, or verbal communication impairments; (8) Long-term excessive alcohol consumption or drug dependence history; (9) are receiving hormone therapy; (10) Pregnant; (11) Those who receive protective medical care or other interventions; (12) Receiving hospice care. Part 2: 1. Medical staff: medical staff who rotate and study; 2. Patients: (1) Speech and communication disorders; (2) unable to cooperate with the interviewer; (3) Protectors of medical conditions; (4) Severe mental illness.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Subjective and objective cognitive function assessment;patient-reported outcomes;Cognitive reserves;Family environment;body composition; | — |
Secondary
| Measure | Time frame |
|---|---|
| Skin fold thickness;Body circumference measurement;Muscle strength measurements; | — |
Countries
China
Contacts
Public ContactLiu Dun
Fujian Medical University
Outcome results
None listed