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The Effectiveness of a Virtual Reality-based Multisensory Intervention

Not Applicable
Not yet recruiting
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
Inclusion Criteria
  1. significant postoperative pain response (VAS score over 4); 2) age greater than 18 years and volunteered to participate in this study.
Exclusion Criteria
  1. 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
NameTimeMethod
Pain responseThe 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.

AnxietyThe 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 qualityThe 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
NameTimeMethod

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