Community health management program for dry eye disease in older adults
Evaluation of the Effectiveness of a Community Health Management Program for Dry Eye Disease in Middle-Aged and Elderly Individuals
This study tests a community health program for older adults with dry eye disease to see if it helps them feel better compared to regular treatments.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 182 (estimated) |
| Ages | 45 Years and up |
| Sex | All |
| Sponsor | Fujian University of Traditional Chinese Medicine Academic / other |
| Locations | 1 site (Fuzhou, Fujian) |
| Trial ID | NCT06443554 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of a community health management program specifically designed for middle-aged and elderly patients suffering from dry eye disease (DED). It compares the outcomes of this community-based approach with conventional treatment methods to assess improvements in eye health and overall quality of life. The program aims to provide tailored support and management strategies to enhance patient care and engagement.
Who should consider this trial
Good fit: Ideal candidates for this study are middle-aged and elderly individuals aged 45 years and above who have been diagnosed with dry eye disease.
Not a fit: Patients with other ocular surface diseases or severe eye conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly improve the quality of life for patients with dry eye disease by providing more effective management strategies.
How similar studies have performed: While there may be limited data on community health management programs specifically for dry eye disease, similar approaches in other chronic conditions have shown promising results.
Eligibility criteria
Show full inclusion / exclusion criteria
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.
Where this trial is running
Fuzhou, Fujian
- The Third People's Hospital Affiliated to Fujian University of Traditional Chinese Medicine — Fuzhou, Fujian, China (Recruiting)
Study contacts
- Study coordinator: Zhang Shiyan
- Email: 2020011012006@stu.hznu.edu.cn
- Phone: 15159718855
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.