hysteromyoma
Conditions
Interventions
Routine oral education group:Routine oral education for preoperative visit
VR+ routine oral education group:Application of virtual reality technology + routine oral education for preoperative visit
Sponsors
Affiliated Hospital of Guangdong Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1. Patients diagnosed with uterine fibroids and scheduled for elective laparoscopic surgery; 2. ASA grading ?~?; 3. Aged 18-75 years; 4. Did not participate in other clinical trials; 5. Patients who can understand and comply with the study and sign the informed consent to participate in the study.
Exclusion criteria
Exclusion criteria: 1. Patients with sleep disorder or chronic insomnia before surgery (preoperative PSQI score > 7 points); 2. Long-term use of sedative and analgesic drugs or sleeping pills and other psychotropic drugs; 3. Patients with poorly controlled or untreated hypertension (resting blood pressure >=180/100mg); 4. Active coronary heart disease, acute cerebrovascular disease or congestive heart disease; 5. Suffering from central nervous system diseases, mental disorders or cognitive dysfunction, and suffering from neurological diseases such as Alzheimer's disease, Parkinson's disease or epilepsy; 6. Moderate and severe hepatic and renal insufficiency; 7. Patients with hearing impairment and/or visual impairment; 8. Patients who cannot wear VR.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| scores of Richard Campbell sleep scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| wearable device record sleep at night;self-rating anxiety scale, SAS;PIttsburgh sleep quality index scale;visual analog pain score,VAS;patient satisfaction; | — |
Countries
China
Contacts
Public ContactZhang Liangqing
Affiliated Hospital of Guangdong Medical University
Outcome results
None listed