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A multicenter clinical trial for visual training to improve visual function in patients with glaucoma

A multicenter clinical trial for visual training to improve visual function in patients with glaucoma

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027036
Enrollment
Unknown
Registered
2019-10-29
Start date
2019-12-01
Completion date
Unknown
Last updated
2019-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glaucoma

Interventions

Test group:Visual training
Control group:Comfort training

Sponsors

West China Hospital,Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with various types of binocular or monocular glaucoma:acute primary angle-closure glaucoma, chronic primary angle-closure glaucoma, primary open-angle glaucoma, secondary glaucoma, and normal intraocular pressure glaucoma. 2. Aged >= 18 years and <= 85 years. 3. Intraocular pressure was controlled at or below the target intraocular pressure by drugs, laser or surgery, and the condition was stable. 4. Can cooperate with visual field examination. 5. Can operate computer mouse. 6. Informed consent can be signed. 7. Can cooperate with long-term training and follow up according to the schedule.

Exclusion criteria

Exclusion criteria: 1. Serious systemic diseases such as cardiovascular and cerebrovascular diseases:cerebral infarction, acute myocardial infarction, malignant tumors,etc.. 2. Non-glaucomatous visual field damage:optic neuritis, ischemic optic neuropathy, papillary edema, craniocerebral diseases, etc.. 3. Fundus oculi disease that affect the results of visual field examination:age-related macular degeneration, retinal artery occlusion, retinal vein occlusion, retinal detachment, uveitis, endophthalmitis, etc.. 4. Severe cataracts make it impossible to obtain visual field test results. 5. Severe dry eye syndrome results in inability to complete computer training.

Design outcomes

Primary

MeasureTime frame
Binocular visual function;

Secondary

MeasureTime frame
Best corrected visual acuity;Contrast sensitivity;Visual field indices;Retinal nerve fiber layer;Ganglion cell complex;Score of life quality of glaucoma patients;Subjects' feelings;

Countries

China

Contacts

Public ContactLi Tang

West China Hospital, Sichuan University

tangli-1a@163.com+86 18980601748

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026