Scar therapy
Conditions
Interventions
Experimental group:Use VR (virtual reality) devices
Control group:None
Sponsors
Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Patient age>=18 years old; Gender is not limited; 2. Scar area =4 points; 4. 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. Severe cognitive impairment; 2. Current or previous diagnosis of epilepsy, dementia, migraine or other neurological diseases that may cause inability to use VR software or possible adverse effects; 3. Presence of conditions sensitive to light stimuli; 4. No stereopsis or severe hearing impairment; 5. There is a condition that may cause injury to the eyes, face or neck, and hinder the use of VR equipment; 6. Severe heart, liver, kidney, blood, digestive, nervous system diseases and malnutrition; 7. Is receiving or plans to receive long-acting analgesic therapy or minimally invasive interventional therapy; 8. Have a history of severe alcohol abuse, or drink heavily for a long time, or have symptoms of alcohol dependence; 9. Current or recent participation (within 1 week) in any analgesic interventional study; 10. Are pregnant or plan to become pregnant during the study; 11. Other situations that the investigator considers unsuitable for participating in clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Virtual reality technology used in scar laser treatment for analgesi; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of adverse events and serious adverse events; | — |
Countries
China
Contacts
Public Contactshiyan
Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Outcome results
None listed