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Survey of Sensory Impairment Indicators Among Adults Aged 65 Years and Older in Xinxing County

A Cross-Sectional Survey of Global Priority Sensory Impairment Indicators Among People Aged 65 Years and Older in Xinxing County

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07694505
Enrollment
2854
Registered
2026-07-10
Start date
2026-07-06
Completion date
2026-12-31
Last updated
2026-07-10

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

Conditions

Cataract, Dual Sensory Impairment, Hearing Loss, Refractive Error, Visual Impairment

Keywords

Effective refractive error coverage, Effective cataract surgical coverage, Effective hearing technology coverage, Older adults, Population-based survey, Cross-sectional study, SENSIIS, WHOears, Xinxing County

Brief summary

This cross-sectional population-based survey will be conducted among residents aged 65 years and older in Xinxing County, Yunfu, Guangdong Province, China. The study will use standardized eye examinations, visual acuity and refractive assessment, anterior segment examination, hearing screening and questionnaires to estimate effective refractive error coverage, effective cataract surgical coverage, effective hearing technology coverage, common eye disease status, and dual sensory impairment among older adults. The findings are intended to provide evidence for primary-level eye and hearing health services.

Detailed description

The study addresses visual impairment, hearing impairment, and dual sensory impairment among older adults in a county-level population. Participants will be recruited from older adults aged 65 years and above covered by the national basic public health service system in Xinxing County. A probability proportional to size cluster sampling method will be used, with village or residential committees as the sampling frame. Study procedures include distance and near visual acuity testing, assessment with habitual correction where applicable, pinhole testing when visual acuity is worse than 6/12, corresponding to decimal visual acuity less than 0.5, slit-lamp examination of the anterior segment, bilateral ear examination, hearing screening using the WHOears app, and relevant questionnaires. Data will be entered and managed electronically and analyzed using descriptive and inferential statistical methods.

Interventions

None listed

Sponsors

Zhongshan Ophthalmic Center, Sun Yat-sen University
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Aged 65 years or older. 2. Voluntarily participates in the study and provides signed informed consent.

Exclusion criteria

1. Unable to cooperate with study-related examinations, including because of disability, communication barriers, or other reasons. 2. Has severe systemic disease that may affect study examinations or make participation potentially hazardous to health. 3. Considered by the investigator to be unsuitable for participation in the study.

Design outcomes

Primary

MeasureTime frameDescription
Effective Refractive Error CoverageAt the cross-sectional survey visit during the 2026-06 to 2026-12 data collection period.Effective refractive error coverage among the surveyed population, calculated at the person level as the proportion of participants with met refractive correction need among all participants with met, under-met, or unmet refractive correction need. The primary threshold will be worse than 6/12 in the better eye, corresponding to decimal visual acuity less than 0.5, with improvement to 6/12 or better through habitual correction, pinhole, or refraction used to classify met, under-met, and unmet need.
Effective Cataract Surgical CoverageAt the cross-sectional survey visit during the 2026-06 to 2026-12 data collection period.Effective cataract surgical coverage among the surveyed population, calculated at the person level as the proportion of participants with operated cataract and a good visual outcome among all participants with operated or operable cataract. Good visual outcome is defined as presenting visual acuity of 6/12 or better; the final operable cataract threshold should be confirmed before release.
Effective Hearing Technology CoverageAt the cross-sectional survey visit during the 2026-06 to 2026-12 data collection period.Effective hearing technology coverage among the surveyed population, calculated as the proportion of participants with moderate or greater hearing loss who regularly use hearing technology and report perceived benefit from its use. Hearing loss classification will be based on WHOears app screening and study questionnaire data.

Secondary

MeasureTime frameDescription
Prevalence and Correction Status of Common Eye DiseasesAt the cross-sectional survey visit during the 2026-06 to 2026-12 data collection period.Prevalence and correction or treatment status of common eye diseases, including refractive error and cataract, based on standardized eye examinations and questionnaire data.
Prevalence of Dual Sensory ImpairmentAt the cross-sectional survey visit during the 2026-06 to 2026-12 data collection period.Prevalence of dual sensory impairment, defined as the proportion of participants who meet both the study visual impairment criterion and the study hearing impairment criterion. The visual impairment criterion will use worse than 6/12 in the better eye, corresponding to decimal visual acuity less than 0.5; the hearing impairment criterion will be based on WHOears app screening and study questionnaire data.
Feasibility and Satisfaction of the SENSIIS System for Primary-Level Vision and Hearing ScreeningAt or after the cross-sectional survey visit during the 2026-06 to 2026-12 data collection period.Feasibility and satisfaction of the SENSIIS system for primary-level vision and hearing screening, assessed through questionnaires and interviews.

Countries

China

Contacts

CONTACTXiaotong Han
hanxiaotong@gzzoc.com086-15999975559
PRINCIPAL_INVESTIGATORLingyi Liang, MD

Zhongshan Ophthalmic Center, Sun Yat-sen University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 11, 2026