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NCT06922838

The Effectiveness of a Virtual Reality-based Multisensory Intervention

Not yet recruiting NA Last updated 11 April 2025
What this trial tests

NA trial testing Virtual Reality intervention in Gynecological Disease in 100 participants. Not yet recruiting.

Timeline
6 April 2025
Primary endpoint
1 July 2025
1 August 2025

Quick facts

Lead sponsorWeifang Medical University
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposesupportive care
Enrollment100
Start date6 April 2025
Primary completion1 July 2025
Estimated completion1 August 2025

Drugs / interventions tested

Conditions studied

Sponsor

Weifang Medical University

Who can join

Adults 18 to 75, female only, with Gynecological Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Effects of multisensory stimulation based on immersive virtual reality in postoperative neuropsychiatric recovery after gynecological laparoscopy.
    Liu J, Liu Y, Bi L, Zhao L, et al · · 2026 · PMID 41872447 · DOI 10.1038/s41746-026-02515-7

Verify or expand the search:

Other trials of Virtual Reality intervention

Trials testing the same drug.

Other Weifang Medical University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06922838.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing