The Effectiveness of a Virtual Reality-based Multisensory Intervention
- Conditions
- Gynecological Disease
- Registration Number
- NCT06922838
- Lead Sponsor
- Weifang Medical University
- Brief Summary
This study explores the effectiveness of a virtual reality-based multisensory intervention for postoperative recovery in patients receiving gynecological surgery.
- Detailed Description
This study explores the effectiveness of a virtual reality-based multisensory intervention for postoperative recovery in patients receiving gynecological surgery. The results of the study included postoperative pain response, comfort, and anxiety of the patients.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- Female
- Target Recruitment
- 100
- significant postoperative pain response (VAS score over 4); 2) age greater than 18 years and volunteered to participate in this study.
- patients with psychosomatic disorders such as delirium, schizophrenia, and bipolar disorder; 2) patients with epilepsy, motion sickness, lightsensitivity, or other neurological diseases may have difficulty wearing the VR headset; 3) patients have severe heart, liver, kidney, blood, digestive, and nervous diseases.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Pain response The pain response of patients was assessed at 0.5 hour, 3 hour, 6 hour, 12 hour, 24 hour postoperatively, and immediately after intervention. The Visual Analog Scale (VAS) scale was used to assess the pain response of patients.
Anxiety The anxiety level of patients was assessed immediately after the intervention. The Beck Anxiety Inventory (BAI) scale was used to assess the anxiety of patients.
Sleep quality The sleep quality of patients was assessed at 24 hour postoperatively. The Pittsburgh Sleep Quality Index (PSQI) scale was used to assess the postoperative sleep quality of patients.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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