此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Prevalence of Presbyopia (Near Vision Fatigue) and Related Factors Among Working Adults Aged 30 to 55 Years in Shanghai (FOCUS)

Prevalence and Associated Factors of Presbyopia Among Working Adults Aged 30-55 Years in Shanghai, China: A Cross-Sectional Study

This observational study aims to determine how common presbyopia is among working adults aged 30-55 years in Shanghai, China, and identify factors associated with it. Presbyopia is an age-related loss of the eye's ability to focus on nearby objects, which can make reading and other close-up activities difficult.

Participants will undergo eye examinations and complete questionnaires about their vision, work activities, use of digital screens, lifestyle, and need for vision correction. The study aims to obtain valid primary outcome data from at least 1,366 participants. It will also assess how closely the results of the NVC mini-program agree with a professional eye examination. No treatment will be assigned as part of the study.

研究概览

地位

尚未招聘

条件

详细说明

This cross-sectional observational study will investigate the prevalence of presbyopia (near fatigue) and associated factors among working adults aged 30-55 years in Shanghai, China. Eligible participants must have worked in their current position for at least one year and provide written informed consent.

Industry-stratified two-stage sampling will be used, with the ISIC Rev.5 classification as the industry stratification framework. At the first stage, workplaces are randomly selected from candidate workplace rosters within each industry stratum; the study plans to include at least 15 independent workplaces covering at least 5 ISIC Rev.5 sections. At the second stage, eligible employees are randomly sampled from complete, de-duplicated employee rosters of the selected workplaces; if the number of eligible employees in a workplace does not exceed the planned invitation quota, all eligible employees are invited. The target is at least 1,366 participants with valid primary outcome data. Allowing for an estimated combined nonresponse and unusable primary outcome data rate of 20%, at least 1,708 individuals will need to be invited.

Data collection will include questionnaires and standardized ophthalmic examinations. Questionnaires will assess demographic and occupational characteristics, near-work demands, screen exposure, sleep, outdoor activities, lifestyle, ocular symptoms, awareness of presbyopia, previous correction, and correction needs and preferences. The NAVQ-P and OSDI questionnaires will assess near-vision difficulties and ocular surface symptoms. Examinations will assess distance, intermediate, and near visual acuity, refraction, near addition power (ADD), accommodative function, and ocular health. NVC mini-program outputs, including presbyopia severity categories and recommended ADD ranges, will also be recorded.

The primary outcome is the prevalence of presbyopia. Presbyopia is defined as binocular near visual acuity worse than N8 at 40 cm under best distance correction, improving by at least one line to N8 or better with additional positive spherical lenses, after excluding other ocular diseases sufficient to explain the reduction in near vision.

Secondary assessments will describe visual function, the relationship between accommodative amplitude and age, awareness of presbyopia, and correction needs. Associations with demographic, occupational, refractive, behavioral, and dry-eye-related factors will be examined. Analyses will account for industry stratification, workplace clustering, and unequal sampling probabilities as appropriate.

Agreement between NVC outputs and subjective refraction ADD will be assessed using overall percent agreement, the proportions of classifications differing by one grade and by two or more grades, and Kendall's tau-b correlation between NVC grades and clinical grades. The proportion of reference ADD values falling within the NVC-recommended ranges will also be calculated. No treatment will be assigned as part of this observational study.

研究类型

观察性的

注册 (估计的)

1366

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Xiangui He MD, PhD
  • 电话号码:021-53555032
  • 邮箱:xianhezi@163.com

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

30年 至 55年 (成人)

接受健康志愿者

是的

有资格学习的性别

全部

取样方法

概率样本

研究人群

Working adults aged 30-55 years employed in their current position for at least one year, recruited from at least 15 independent workplaces in Shanghai covering at least 5 ISIC Rev.5 industry sectors (education; manufacturing; construction; human health and social work activities; financial and insurance activities; public administration; professional, scientific and technical activities; administrative and support service activities). Within each workplace, eligible employees are randomly sampled from complete, de-duplicated rosters; if eligible employees do not exceed the planned invitation quota, all are invited. Participants are examined regardless of presbyopia status; the target population includes people with and without presbyopia.

描述

Inclusion Criteria:

  • Aged 30 to 55 years inclusive, based on date of birth on the national identification card
  • Either sex
  • Employed in the current position for at least one year
  • Willing to participate and able to provide written informed consent
  • Able to complete the questionnaire and the ophthalmic examinations

Exclusion Criteria:

  • Active ocular inflammation, significant ocular trauma, or other acute ocular condition within the past 3 months that precludes visual function testing
  • Previous intraocular surgery that substantially affects refractive status or visual function assessment, such as cataract surgery or refractive lens surgery
  • Obvious cognitive impairment, severe psychiatric disease, or other condition preventing cooperation with the survey and examinations
  • Markedly reduced best-corrected distance visual acuity with ocular disease sufficient to explain the near vision abnormality, including but not limited to adult amblyopia, significant corneal scarring, keratoconus, severe corneal dystrophy, significant lens opacity, and severe macular or optic nerve disease
  • Severe fundus or optic nerve disease, including macular degeneration, significant maculopathy, retinal detachment, optic atrophy or advanced glaucoma
  • Any other condition judged by the investigators to make participation unsuitable

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 观测模型:COHORT
  • 时间观点:CROSS_SECTIONAL

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Prevalence of presbyopia among working adults aged 30 to 55 years in Shanghai
大体时间:Day 1 (At the single study visit (cross-sectional assessment))

Proportion of participants meeting the study definition of presbyopia: binocular near visual acuity worse than N8 (equivalent to 20/50) at 40 cm under standard illumination with full distance refractive correction, improving by at least one line to N8 or better after binocular addition of plus lenses, after exclusion of organic ocular disease that could independently explain reduced near vision. Reported as a percentage with 95 percent confidence interval, overall and stratified by 5-year age group, sex, occupation, education level, refractive status and screen exposure level.

Day 1 (At the single study visit (cross-sectional assessment))

次要结果测量

结果测量
措施说明
大体时间
Amplitude of accommodation by age group
大体时间:Day 1 (At the single study visit (cross-sectional assessment))

Amplitude of accommodation in diopters, measured by the push-up method under full distance correction, repeated three times per eye and averaged. Reported as mean and standard deviation or median and interquartile range by 5-year age group, and used to fit the accommodation-age curve.

Day 1 (At the single study visit (cross-sectional assessment))
Adjusted odds ratios for factors associated with presbyopia
大体时间:Day 1 (At the single study visit (cross-sectional assessment))

Association of presbyopia with age, sex, education level, occupation and job type, refractive status, near-work duration, screen exposure, sleep duration and quality, outdoor activity and dry eye measures, estimated by generalized estimating equations or mixed-effects logistic regression with workplace as a clustering variable or random effect. Reported as adjusted odds ratios with 95 percent confidence intervals.

Day 1 (At the single study visit (cross-sectional assessment))
Awareness of presbyopia and need for near vision correction
大体时间:Day 1 (At the single study visit (cross-sectional assessment))

Description: Questionnaire-based assessment of awareness and understanding of presbyopia, previous care-seeking, current correction methods and wearing time, acceptance of correction options, acceptable price range, and future intention to use correction. Near vision-related quality of life assessed with the Chinese version of the Near Activity Visual Questionnaire for Presbyopia (NAVQ-P). Reported as frequencies and percentages.

Day 1 (At the single study visit (cross-sectional assessment))
Correlation between presbyopia severity grade and dry eye severity grade
大体时间:Day 1 (At the single study visit (cross-sectional assessment))

Dry eye graded as mild, moderate or severe based on the Ocular Surface Disease Index (OSDI), non-invasive tear break-up time, tear meniscus height and slit-lamp findings. Correlation with presbyopia severity grade assessed by Spearman rank correlation and, where appropriate, ordinal logistic regression adjusted for age, sex, refractive status, screen exposure and near-work load.

Day 1 (At the single study visit (cross-sectional assessment))
Agreement between NVC mini-program outputs and subjective refraction
大体时间:Day 1 (At the single study visit (cross-sectional assessment))

The near-fatigue severity grade and recommended ADD range output by the NVC mini-program will be compared with the reference ADD obtained by subjective refraction. Agreement measures include overall percent agreement, the proportion of classifications differing by one grade, the proportion differing by two or more grades, and Kendall's tau-b correlation between NVC grades and clinical grades. The proportion of reference ADD values falling within the NVC-recommended ranges will also be calculated.

Day 1 (At the single study visit (cross-sectional assessment))

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年11月1日

初级完成 (估计的)

2027年1月1日

研究完成 (估计的)

2027年1月1日

研究注册日期

首次提交

2026年11月3日

首先提交符合 QC 标准的

2026年11月6日

首次发布 (实际的)

2026年11月9日

研究记录更新

最后更新发布 (实际的)

2026年11月9日

上次提交的符合 QC 标准的更新

2026年11月6日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • IIT2026-015

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅