Actively Recruiting

Phase Not Applicable
All Genders
NCT06964867

Effectiveness of Multimedia Health Education to Reduce Anxiety in Patients With Vitreous Floaters

Led by Changzhou No.2 People's Hospital · Updated on 2025-05-14

300

Participants Needed

1

Research Sites

78 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The patients with vitreous floaters were randomly divided into to groups after excluding the possibility of coexisting ocular pathologies potentially confounding visual symptoms or vitreoretinal anatomy. The control group performed conventional oral education. The experimental group conducted multimedia health education activities on the basis of conventional oral education. Their VRQoL (Visual Function Questionnaire-25, VFQ-25) and anxiety status (State-Trait Anxiety Inventory, STAI) were evaluated before education and at the final follow-up. The demographic and clinical characteristics (gender, age, eduaction, duration of vitreous floaters, comorbidities and so on) were collected.

CONDITIONS

Official Title

Effectiveness of Multimedia Health Education to Reduce Anxiety in Patients With Vitreous Floaters

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinical diagnosis of vitreous floaters
  • Ability to complete questionnaires
Not Eligible

You will not qualify if you...

  • Secondary vitreous floaters requiring surgical intervention
  • Other eye diseases affecting vitreoretinal anatomy
  • History of vitreoretinal surgery

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

the Second People's Hospital of Changzhou

Changzhou, Jiangsu, China, 213100

Actively Recruiting

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Research Team

Q

Qing Feng

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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