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The Effectiveness of a Virtual Reality-based Multisensory Intervention

Effectiveness of a Virtual Reality-based Multisensory Intervention for Postoperative Recovery in Patients Receiving Gynecological Surgery

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06922838
Enrollment
100
Registered
2025-04-11
Start date
2025-04-06
Completion date
2025-08-01
Last updated
2025-04-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gynecological Disease

Keywords

Pain management, Virtual reality, Gynecology, Postoperative recovery

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.

Interventions

The head-mounted virtual reality device is used to provide patients with relaxing videos of nature scenes accompanied by calming music and guided meditations.

OTHERAromatherapy

The cotton ball soaked in lavender essential oil is placed near the patient's pillow.

Sponsors

Weifang Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 75 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
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.

Contacts

Primary ContactShirong Fang, M.D
fsr0536@163.com15094947165

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 25, 2026