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The application effect of virtual reality on postoperative pain management of patients with Crohn's disease

The application effect of virtual reality on postoperative pain management of patients with Crohn's disease

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081109
Enrollment
Unknown
Registered
2024-02-22
Start date
2023-03-17
Completion date
Unknown
Last updated
2024-02-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Crohn's disease?postoperative pain

Interventions

Control group:Clinical routine postoperative analgesia
Experimental group 1:15 minutes VR video on the first postoperative day
Experimental group 2:Provide 15 minutes of VR video on the first and second postoperative days, respectively

Sponsors

Affiliated Sir Run Run Shaw Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Conforming to the diagnostic criteria of CD in theChinese consensus on diagnosis and treatment of inflammatory bowel disease(Beijing, 2018) the patient was diagnosed with CD through imaging, endoscopy, histology, pathology, etc 2. Age=18 3. Operation with bowel segment resection 4. Postoperative use of patient-controlled intravenous analgesia 5. Voluntarily participate in this study and sign an informed consent form

Exclusion criteria

Exclusion criteria: 1. Those undergoing simultaneous multiorgan resection 2. Transferred to ICU monitor postoperatively 3. Patients were critically ill or unable to cooperate in the perioperative period 4. Preoperative use of opioid analgesics; 5. Individuals who are sensitive to virtual reality and 3D scenes and cannot tolerate them; 6. History of epileptic seizures; 7. Individuals with visual or auditory impairments. 8. Vulnerable groups include critically ill patients, mental illness sufferers, cognitive impairment sufferers, minors, pregnant women, illiterates, etc.

Design outcomes

Secondary

MeasureTime frame
Opioid consumption;The degree of anxiety depression;Hospitalization duration;Hospital costs;Pain control in patients with satisfaction;

Primary

MeasureTime frame
worst postoperative pain intensity;

Countries

China

Contacts

Public ContactZhang Xiaoming

Affiliated Sir Run Run Shaw Hospital, Zhejiang University School of Medicine

zhangxm@srrsh.com+86 151 6827 8628

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026