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Community-Based Eye Screening With Structured Referral Tracking for Preventing Avoidable Blindness in Adults in Rawalpindi, Pakistan (SIGHT)

2026年6月2日 更新者:Khizar Nabeel、Health Services Academy, Islamabad, Pakistan

Community-Based Eye Screening With a Structured Referral Tracking Intervention for the Prevention of Avoidable Blindness Among Adults in Rawalpindi District, Pakistan

This cluster randomized controlled trial aims to evaluate the effectiveness of a Structured Referral Tracking (SRT) intervention in improving referral completion among adults identified with avoidable blindness during community-based eye screening camps in Rawalpindi District, Pakistan. Ten community clusters will be randomized into intervention and control groups. Participants in the intervention group will receive structured referral counseling, weekly reminder calls or messages, and customized referral guidance for eight weeks, while the control group will receive standard referral procedures. The primary outcome is referral completion at a tertiary eye hospital within eight weeks after screening. Secondary outcomes include knowledge regarding avoidable blindness, treatment satisfaction, feasibility, acceptability, and barriers influencing referral completion.

研究概览

详细说明

Avoidable blindness remains a major public health challenge in low- and middle-income countries, including Pakistan. Community-based eye screening camps are commonly used to identify individuals with visual impairment and eye diseases requiring treatment; however, referral completion to tertiary eye care facilities remains poor. Many patients fail to attend referral hospitals because of limited awareness, lack of follow-up, transportation barriers, and uncertainty regarding treatment procedures.

This study aims to evaluate the effectiveness and implementation of a Structured Referral Tracking (SRT) intervention in improving referral completion among adults identified with avoidable blindness during community-based eye screening camps in Rawalpindi District, Pakistan.

The study will use a cluster randomized controlled trial design. Ten community clusters (union councils) from five tehsils of Rawalpindi District will be selected using multistage random sampling. Clusters will be randomized into intervention and control arms. Participants attending eye screening camps who are diagnosed with eye conditions requiring referral to a tertiary eye hospital will be enrolled after informed consent.

Participants in the intervention arm will receive a multi-component Structured Referral Tracking intervention consisting of referral counseling, weekly reminder calls or mobile messages, visual educational material, and customized referral guidance regarding hospital location, estimated costs, and required documents. Participants in the control arm will receive standard referral procedures consisting of routine counseling and referral slips without structured follow-up.

The primary outcome will be referral completion at the tertiary eye hospital within eight weeks after screening, verified through hospital attendance records. Secondary outcomes will include knowledge regarding avoidable blindness, treatment satisfaction, feasibility and acceptability of the intervention, and barriers influencing referral completion.

The findings of this study are expected to provide evidence regarding the effectiveness and feasibility of structured referral tracking systems for improving eye care service utilization and reducing avoidable blindness in Pakistan.

研究类型

介入性

注册 (估计的)

500

阶段

  • 不适用

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:Khizar Nabeel, PHD (In progress)
  • 电话号码:+923455096776
  • 邮箱:khizar@hsa.edu.pk

学习地点

    • Punjab Province
      • Rawalpindi、Punjab Province、巴基斯坦、46600
        • ACCO Department, Al-Shifa Trust Eye Hospital, Rawalpindi

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

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  • Adults aged 18 years or above
  • Individuals diagnosed with visual impairment or eye conditions requiring referral to a tertiary eye care facility
  • Permanent residents of Rawalpindi District, Pakistan
  • Willing and able to provide informed consent

Exclusion Criteria:

  • Individuals already undergoing treatment for the identified eye condition
  • Individuals requiring emergency ophthalmic care
  • Severe systemic or physical illness limiting follow-up
  • Individuals unable to provide informed consent

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

  • 主要用途:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Structured Referral Tracking (SRT)
Participants will receive structured referral counseling, weekly reminder calls or messages, visual educational material, and customized referral guidance for eight weeks following community-based eye screening.
A multi-component referral tracking intervention including referral counseling, weekly reminder calls or mobile messages, visual educational material, and customized referral guidance to improve referral completion after community eye screening.
无干预:Standard Referral Procedure
Participants will receive routine referral slips and standard counseling without structured follow-up or reminder communication.

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
Referral Completion Rate Verified Through Hospital Records
大体时间:Within 8 weeks after community eye screening
Proportion of referred participants who complete referral visits at the tertiary eye hospital, verified through hospital attendance records.
Within 8 weeks after community eye screening

次要结果测量

结果测量
措施说明
大体时间
Knowledge Score on Avoidable Blindness Questionnaire
大体时间:Baseline and 8 weeks after screening
Participant knowledge regarding avoidable blindness and eye health assessed using a structured questionnaire developed for the study.
Baseline and 8 weeks after screening
Participant Acceptability of Structured Referral Tracking Assessed Using Structured Feedback Questionnaire
大体时间:Within 8 weeks after screening
Participant acceptability of the Structured Referral Tracking intervention assessed using a structured feedback questionnaire regarding usefulness and satisfaction with reminder communication.
Within 8 weeks after screening
Barriers Influencing Referral Completion Assessed Using Structured Barrier Assessment Questionnaire
大体时间:Within 8 weeks after screening
Barriers and facilitators influencing referral completion assessed using a structured questionnaire among referred participants.
Within 8 weeks after screening

其他结果措施

结果测量
措施说明
大体时间
Participant Treatment Satisfaction Score Using Structured Satisfaction Questionnaire
大体时间:Within 8 weeks after screening
Participant-reported satisfaction regarding referral services and treatment received at the tertiary eye hospital assessed using a structured satisfaction questionnaire.
Within 8 weeks after screening
Feasibility of Structured Referral Tracking Assessed by Reminder Delivery and Follow-up Completion Rates
大体时间:Within 8 weeks after screening
Feasibility of the intervention assessed through successful delivery of reminder messages/calls and completion of scheduled follow-up procedures.
Within 8 weeks after screening

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。

调查人员

  • 研究主任:Dr. Ahmad Abdullah, PHD、Shifa International Hospital, Islamabad

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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6月1日

初级完成 (估计的)

2026年6月1日

研究完成 (估计的)

2026年11月30日

研究注册日期

首次提交

2026年5月13日

首先提交符合 QC 标准的

2026年5月20日

首次发布 (实际的)

2026年5月28日

研究记录更新

最后更新发布 (实际的)

2026年6月4日

上次提交的符合 QC 标准的更新

2026年6月2日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

IPD 计划说明

De-identified individual participant data underlying the published results may be shared upon reasonable request after publication of the primary study findings.

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.

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