Obesity
Conditions
Interventions
Intervention Group:Preoperative VR intervention in addition to routine preoperative consultation and standardized anesthesia.
Control Group:Routine preoperative consultation and standardized anesthesia only.
Sponsors
The Affiliated Hospital of Xuzhou Medical University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.American Society of Anesthesiologists (ASA) Physical Status Classification II-III; 2.Aged >=18 years; 3.Undergoing elective laparoscopic bariatric surgery for the first time; 4.No preoperative gastrointestinal diseases; 5.Possessing basic audio-visual abilities;
Exclusion criteria
Exclusion criteria: 1. Emergency surgery; 2. Severe mental illness (e.g. schizophrenia, acute phase of major depression) or cognitive impairment; 3. A history of motion sickness or a tendency to experience severe discomfort (nausea, dizziness) following VR exposure; 4. Recent use of medications that may significantly affect anxiety levels (e.g. benzodiazepines) or gastrointestinal motility (e.g. high-dose opioid analgesics, prokinetic agents, antiemetics) 5. Known severe vestibular dysfunction 6. Skin conditions unsuitable for wearing VR headsets 7. Participation in other intervention studies that may affect anxiety or gastrointestinal function
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time to first flatus;Anxiety score;Sleep score;Postoperative pain score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Antiemetic use;Postoperative gastrointestinal function score;Time to first ambulation;Postoperative Nausea and Vomiting;Adverse events following VR intervention;Opioid consumption (morphine milligram equivalents);Emergence agitation score;Length of hospital stay; | — |
Countries
China
Contacts
Public ContactYueying Zhang
The Affiliated Hospital of Xuzhou Medical University
Outcome results
None listed