Clinical Trial

Effect of Video Viewing on Intravitreal Injection Experience

Recruiting
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Record status
This record was last updated June 3, 2025 (before its estimated August 5, 2025 completion). Its status may not reflect the trial's current state.
Summary
Study Objective The goal of this clinical trial is to evaluate whether viewing a procedural video can improve the patient experience and reduce the incidence and severity of subconjunctival hemorrhage in individuals undergoing intravitreal anti-VEGF injections. Key Research Questions 1. Can viewing the procedural video prior to treatment reduce the rate and/or area of subconjunctival hemorrhage? 2. Can the video improve the patient experience, specifically by reducing anxiety levels and increasing satisfaction with the treatment process? Study Design Participants will be randomly assigned to either an intervention group, who will watch an educational video explaining the injection procedure, or a control group, who will not view the video. All participants will complete the State-Trait Anxiety Inventory-State (STAI-S) questionnaire both before and after treatment to assess changes in anxiety levels.
Protocol Amendment History 1 change
notable Sponsor changed: Second Affiliated Hospital, School of Medicine, Zhejiang University -> Second Affiliated Hospital, Zhejiang University, School of Medicine 2026-08-09
Trial Details
NCT Number NCT07002372
Lead Sponsor Second Affiliated Hospital, School of Medicine, Zhejiang University
Conditions Age Related Macular Degeneration, Diabetic Retinopathy, Choroidal Neovascularization, Retinal Vein Occlusion, Cystoid Macular Edema
Enrollment 182 participants
Start Date 2025-05-05
Primary Completion 2025-08-05 (estimated)
Study Completion 2025-10-05 (estimated)
Updated on ClinicalTrials.gov 2025-06-03