colorectal cancer
Conditions
Interventions
preoperative group:None
postoperative group:None
Family group of the interviewee:None
pre-lab group:To set of the scheme as an aid to shared decision-making on nutritional therapy for patients
Sponsors
The First Affiliated Hospital of Shantou University Medical College
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Qualitative Study 1: Preoperative group: 1)Comply with CRC diagnosis and treatment guidelines, and plan to perform radical CRC surgery; 2)NRS2002 evaluation of nutritional risk; 3)have been nutritional treatment; 4)no serious life-threatening complications; 5)informed about the content of the study and methodology, and signed an informed consent; 6)Age >= 18 years old. 2: Postoperative group: 1) Comply with CRC diagnosis and treatment guidelines, 1-2 weeks after radical CRC surgery; 2) NRS2002 assessment of nutritional risk; 3) nutritional treatment; 4) no serious life-threatening complications; 5) informed about the content and method of the study, signed an informed consent form; 6) age >= 18 years old. 3: Family members group: 1) participate in the nutritional treatment of the patients; 2) be informed of the content and method of the study and sign the informed consent form; 3) age >= 18 years old. Pre-lab 1 patients meet the guidelines for diagnosis and treatment of CRC, and plan to undergo radical CRC surgery or postoperative day 1-2; 2 Nutritional Risk Screening NRS2002 rating >= 3 points; 3 no serious life-threatening complications; 4 informed about the study content and methodology, can cooperate, and sign an informed consent form; 5 age >= 18 years old.
Exclusion criteria
Exclusion criteria: Qualitative Study 1: Preoperative group: 1) history of mental illness; 2) communication and cognitive disorders; 3)combination of other serious diseases; 4) various reasons for not completing the interview. 2: Postoperative group: 1) history of mental illness;2) communication and cognitive disorders; 3) other serious diseases; 4)various reasons for not completing the interview. 3: Family members group: 1) history of mental illness; 2)communication and cognitive disorders; 3) various reasons for not completing the interview. Pre-lab 1) explicitly refused to participate in decision-making or family members refused to inform the patients; 2) serious underlying diseases, critical conditions or life-threatening complications that prevented them from cooperating; 3) history of mental illness; 4) communication disorders and cognitive disorders; 5) various reasons for not completing the experiment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| attitude of participation in treatment decision-making;Satisfaction with participation in medical decision-making; | — |
Countries
China
Contacts
Public ContactChanshan Ma
The First Affiliated Hospital of Shantou University Medical College
Outcome results
None listed