Gastric cancer, colorectal cancer, ileus
Conditions
Interventions
Experimental group:Use virtual reality equipment
Control group:Routine medical care measures
Sponsors
West China Hospital, Sichuan University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1.Aged 18 to 80 years; 2.Patients who have undergone gastric or intestinal surgery; 3.Can cooperate with nurses to use virtual reality operators; 4.Signed informed consent and voluntarily participated in the study.
Exclusion criteria
Exclusion criteria: 1.Pregnant or lactating women, mentally ill; 2.Patients with serious and uncontrolled organic diseases or infections, such as decompensated heart, lung, kidney failure, and other life-threatening diseases at any time; 3.Patients with intestinal obstruction, gastric or intestinal perforation, chronic enteritis and other diseases that affect intestinal function greatly; 4.People with a history of or high risk of gastrointestinal ulcer; 5.Use probiotics, yogurt or probiotics powder and other microecological probiotics, metformin, proton pump inhibitors and berberine in the last 1 month; 6.History of motion sickness, such as Meniere's syndrome or otoliasis; 7.Preoperative radiotherapy and chemotherapy; 8.Concomitant use of other experimental drugs; 9.Other clinical trial participants.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intestinal microflora diversity and community structure distribution;Diamine oxidase;Intestinal fatty acid binding protein;Time of first postoperative defecation;Time of first postoperative exhaust;Recovery time of first bowel sounds; | — |
Secondary
| Measure | Time frame |
|---|---|
| Plasma orexin A;Appetite ratings;Abdominal distension score;Time of first postoperative ambulation;Time of first oral feeding after surgery;Length of stay;Quality of life score;Comfort score; | — |
Countries
China
Contacts
Public ContactLi Ka
West China Hospital, Sichuan University
Outcome results
None listed