Actively Recruiting

Phase Not Applicable
Age: 45Years +
All Genders
NCT06443554

Evaluation of the Effectiveness of a Community Health Management Program for Dry Eye Disease in Middle-Aged and Elderly Individuals

Led by Fujian University of Traditional Chinese Medicine · Updated on 2024-06-05

182

Participants Needed

1

Research Sites

47 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study evaluates the effectiveness of a community health management program for middle-aged and elderly patients with dry eye disease (DED). By comparing the community-based health management plan with conventional treatment, the study aims to determine the impact on eye health and quality of life.

CONDITIONS

Official Title

Evaluation of the Effectiveness of a Community Health Management Program for Dry Eye Disease in Middle-Aged and Elderly Individuals

Who Can Participate

Age: 45Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients meeting the diagnostic criteria for dry eye disease.
  • Middle-aged and elderly individuals aged 45 years and above.
  • Normal cognitive and expressive abilities.
  • Informed consent and ability to complete the survey.
  • Voluntary participation in the study.
Not Eligible

You will not qualify if you...

  • Patients with other ocular surface diseases, including stye, trachoma, allergic conjunctivitis, etc.
  • Patients with severe cataracts, glaucoma, uveitis, retinal detachment, optic nerve diseases, high myopia, or other conditions.
  • Patients who have undergone eye surgery or have a history of eye trauma in the past three months.
  • Patients who did not sign the informed consent form.

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 Third People's Hospital Affiliated to Fujian University of Traditional Chinese Medicine

Fuzhou, Fujian, China, 350000

Actively Recruiting

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Research Team

Z

Zhang Shiyan

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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