None listed
Conditions
Interventions
Experimental Group:Patients in the experimental group will receive postoperative analgesic adjunctive therapy software to assist in pain control, with one postoperative analgesic adjunctive therapy so
Control Group:The control group will not experience postoperative analgesic adjuvant therapy software and will only record the pain level within 30 minutes. Subjects will complete a study summary form
Sponsors
Guangdong Provincial People's Hospital
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Age greater than or equal to 18 years. 2. Patients within 1 day after thoracoscopic surgery. 3. Junior high school degree or above, Mandarin communication is unimpeded, with certain Internet knowledge and mobile phone reading and writing skills. 4. The score of the numeric grading scale (NRS) at 24 hours postoperatively = 4 points. 5. Patients who are able to understand the purpose of the study, voluntarily participate in and sign the informed consent form, and are willing to complete the follow-up as required by the protocol.
Exclusion criteria
Exclusion criteria: 1. Patients with severe cognitive impairment. 2. Patients with a previous diagnosis of epilepsy, dementia, migraine, or other neurological disease that may result in the inability to use postoperative analgesic adjuvant therapy software or that may have adverse effects. 3. Patients who are unable to understand or speak Mandarin. 4. Patients who have visual abnormalities, severe hearing impairment, or motion sickness, etc., and are unable to view VR. 5. Patients with trauma to the eyes, face, or neck that prevents the comfortable use of the VR device. 6. Patients with severe heart, liver, kidney, hematologic, digestive, nervous system diseases and malnutrition. 7. Patients who have previously used virtual reality software for pain that has not responded to treatment. 8. Patients with a history of severe alcohol abuse, long-term heavy drinking, and symptoms of alcohol dependence. 9. Patients who have participated in any analgesic interventional study within the past 1 week. 10. Females who are pregnant or plan to become pregnant during the study. 11. The patient or their immediate family member works for a digital health or pharmaceutical company for acute or chronic pain treatment. 12. Patients who are unable to use electronic devices such as smartphones. 13. Other conditions that the investigator considers inappropriate for participation in a clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Numeric Rating Scale (NRS); | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of adverse events and Incidence of serious adverse events; | — |
Countries
China
Contacts
Public ContactWenzhao Zhong
Guangdong Provincial People's Hospital
Outcome results
None listed