ClinicalTrials.Veeva

Menu

The Effectiveness of a Virtual Reality-based Multisensory Intervention

W

Weifang Medical University

Status

Not yet enrolling

Conditions

Gynecological Disease

Treatments

Other: Aromatherapy
Other: Virtual Reality intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT06922838
2025YX406

Details and patient eligibility

About

This study explores the effectiveness of a virtual reality-based multisensory intervention for postoperative recovery in patients receiving gynecological surgery.

Full 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.

Enrollment

100 estimated patients

Sex

Female

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

100 participants in 3 patient groups

VR-Aromatherapy group
Other group
Description:
The VR-Aromatherapy group received virtual reality intervention combined with aromatherapy for 20 minutes postoperatively. The intervention was started by an investigator from the return of the patient to the ward.
Treatment:
Other: Virtual Reality intervention
Other: Aromatherapy
Aromatherapy group
Other group
Description:
The Aromatherapy group received lavender aromatherapy for 20 minutes postoperatively. The intervention was started by an investigator from the return of the patient to the ward.
Treatment:
Other: Aromatherapy
VR group
Other group
Description:
The VR group received virtual reality intervention for 20 minutes postoperatively. The intervention was started by an investigator from the return of the patient to the ward.
Treatment:
Other: Virtual Reality intervention

Trial contacts and locations

0

Loading...

Central trial contact

Shirong Fang, M.D

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems