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临床试验/NCT06124521
NCT06124521招募中不适用

Increasing Eye Care Utilization in Black Americans At High Risk For Glaucoma Using A Community-Engaged and Faith-Based Intervention

University of Michigan2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年10月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
2
主要终点
Eye care utilization

研究概览

简要总结

The purpose of this research is to evaluate if intervention and education can change the behavior of someone's willingness to see an eye care provider to prevent blindness and glaucoma. The researchers are investigating if adding additional resources improves participant access to care.

详细描述

Outcome measures related to acceptability and feasibility are exploratory. They will not be registered or results reported.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Black or African American
  • Participated in the screening examination portion of the study

排除标准

  • Current eye pain (> 8 out of 10)
  • Sudden decrease in vision (within 1 week)
  • Double vision that doesn't stop when you blink and stops no matter what eye you cover (not blurred, but seeing 2 objects)
  • Pregnant women
  • Prisoners
  • Cognitive impairment- unable to give an ocular and social history
  • Moving outside of Michigan or driving distance to the church within 6 months

研究组 & 干预措施

Eye concern

Experimental

Those with a diagnosis of glaucoma or glaucoma suspect (or other concerning eye disease, such as diabetic retinopathy or macular degeneration) will be invited to participate in the ComBaT Glaucoma.

干预措施: ComBaT Glaucoma (Behavioral)

结局指标

主要结局

Eye care utilization

时间窗: Up to 14 months

Participants who have not seen an eye care provider for an initial clinical evaluation within 6 months of entering the program or a follow-up evaluation at 12 months will be considered underutilizers. Those who have received evaluation at 6 and 12 months will be considered normal utilizers.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Angela Elam

Assistant Professor of Ophthalmology and Visual Sciences

University of Michigan

研究点 (2)

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