preoperative anxiety
Conditions
Interventions
Experimental group:Watch VR video before surgery
Control group:no intervention
Sponsors
Fuxing Hospital Affiliated to Capital Medical University
Eligibility
Sex/Gender
Female
Age
30 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Patients undergoing gynecological laparoscopic surgery; 2. To be operated under general anesthesia; 3. Age 30-60 years old; 4. BMI 18.5-30 kg/m2 5. ASA I-II level; 6. The preoperative pain score is 0; 7. Understand the informed consent form and agree to sign the informed consent form before this study.
Exclusion criteria
Exclusion criteria: 1. ASA >= III level; 2. Patients with severe mental disorders; 3. Patients with chronic pain before operation; 4. Patients with severe lung, heart, liver, and cerebrovascular diseases; 5. Patients who are allergic to the drugs used in the experiment; 6. Abnormal vision, suffering from motion sickness, unable to watch VR patients; 7. Patients who cannot understand the informed consent form; 8. Patients using sedative drugs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| postoperative acute pain visual analogue scale score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Hospital Anxiety and Depression Scale (HADS) score changes before and after intervention; | — |
Countries
China
Contacts
Public ContactLi Tianzuo
Fuxing Hospital Affiliated to Capital Medical University
Outcome results
None listed