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Glaucoma is the leading cause of irreversible blindness worldwide. The visual function of patients with advanced glaucoma is severely impaired, and the vision-related activities (e.g. movement, reading) are obviously restricted, which may have a negative impact on the patients' quality of life (QOL) and increase the burden on individuals and families. Low vision aids (LVAs) and other devices for vision rehabilitation (VR) are useful for patients with advanced glaucoma to maximize the function of residual vision and improve the QOL. OXSIGHT smart glasses are the latest LVAs eyeglasses that are expected to improve the QOL for patients with low vision (LV), such as those with glaucoma. Clinical data were collected to evaluate the efficacy and its influencing factors of OXSIGHT smart glasses in patients with advanced glaucoma, in providing theoretical basis for subsequent clinical studies.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| OXSIGHT smart glasses | Experimental | Wearing OXSIGHT smart glasses |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| OXSIGHT smart glasses | Device | OXSIGHT smart glasses are head-mounted electronic LVAs designed for LV patients with visual field loss. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Changes from baseline CLVQOL scores at different time points | The Low vision Quality of Life Questionnaire (LVQOL) specifically investigates the QOL of visually impaired patients. The questionnaire consists of 25 closed items and examines four dimensions: distance vision, mobility and lighting; adjustment; reading and fine work; daily activities. As a convenient tool, LVQOL is widely used in clinical settings to evaluate effects of clinical treatment and corresponding strategies of low-vision rehabilitation. CLVQOL is the Chinese version of LVQOL. | The examination was performed at 1 day, 1 week, 2 weeks, 4 weeks and 8 weeks after intervention. |
| Measure | Description | Time Frame |
|---|---|---|
| Changes from baseline visual acuity at different time points | ETDRS visual acuity chart was used. | The examination was performed at 1 day, 1 week, 2 weeks, 4 weeks and 8 weeks after intervention. |
| Changes from baseline contrast sensitivity at different time points |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Yiqing Li, doctor | Contact | 13302235127 | liyiqing@gzzoc.com | |
| Zhidong Li, doctor | Contact | 15521059530 | aiyou1989@163.com |
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| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 11673287 | Background | Foster PJ, Johnson GJ. Glaucoma in China: how big is the problem? Br J Ophthalmol. 2001 Nov;85(11):1277-82. doi: 10.1136/bjo.85.11.1277. | |
| 16488940 | Result | Quigley HA, Broman AT. The number of people with glaucoma worldwide in 2010 and 2020. Br J Ophthalmol. 2006 Mar;90(3):262-7. doi: 10.1136/bjo.2005.081224. |
| Label | URL |
|---|---|
| The Number of People With Glaucoma Worldwide in 2010 and 2020 | View source |
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Pelli-Robson Contrast Sensitivity Charts were used. |
| The examination was performed at 1 day, 1 week, 2 weeks, 4 weeks and 8 weeks after intervention. |
| Changes from baseline visual field at different time points | Visual field was measured by the kinetic perimetry test of Humphrey field analyzer. | The examination was performed at 1 day, 1 week, 2 weeks, 4 weeks and 8 weeks after intervention. |
| Changes from baseline scores of mobility test at different time points | A mobility test was performed to evaluate patients' functionality in 2 scenarios: using their best-corrected visual acuity with no LVAs and using the OXSIGHT Smart Glasses. A loop-shaped obstacle course consisting of stationary obstacles from floor to head level was designed for this test. | The examination was performed at 1 day, 1 week, 2 weeks, 4 weeks and 8 weeks after intervention. |
| Glaucoma in China: How Big Is the Problem? | View source |