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

F

Fujian University of Traditional Chinese Medicine

Status

Enrolling

Conditions

Dry Eye Disease

Treatments

Procedure: Health Management Intervention Program
Procedure: Standard Treatment

Study type

Interventional

Funder types

Other

Identifiers

NCT06443554
2023ks-61-1

Details and patient eligibility

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.

Enrollment

182 estimated patients

Sex

All

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients meeting the diagnostic criteria for dry eye disease.
  2. Middle-aged and elderly individuals aged 45 years and above.
  3. Normal cognitive and expressive abilities.
  4. Informed consent and ability to complete the survey.
  5. Voluntary participation in the study.

Exclusion criteria

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

182 participants in 2 patient groups, including a placebo group

Intervention group
Experimental group
Treatment:
Procedure: Health Management Intervention Program
Control group
Placebo Comparator group
Treatment:
Procedure: Standard Treatment

Trial contacts and locations

1

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Central trial contact

Zhang Shiyan

Data sourced from clinicaltrials.gov

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