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Impact of Automated Calls on Pediatric Patient Attendance in Chile (Health Call)

Health Call: A Randomized Control Trial of Interactive Automated Reminder Calls to Reduce Failure to Attend Rates at an Urban Referral Hospital in Chile

Missed health care appointments present a serious challenge to patient care. Especially in government funded health systems like that of Chile, missed appointments can lead to delayed care, wasted resources, and escalating costs.

This private-public-research collaboration seeks to provide a rigorous, practical evaluation of a new patient reminder system, evaluate how health beliefs impact patient attendance, and capture the potential for scaling up this or other health technology systems. Using a mixed-methods approach this study will provide contextualized, triangulated analysis of pediatric patient attendance in Chile.

研究概览

地位

完全的

条件

详细说明

The Health Call study is divided into two phases. The first phase is a randomized controlled trial and side-by- side cost-benefit analysis. Enrolled guardians of pediatric patients will complete a questionnaire at the point of referral and then be randomized to intervention, the automated reminder system, or no reminder. The investigators will then monitor attendance status at their subsequent appointment and evaluate whether the appointment reminders affected attendance as well as the cost-benefit ratio of using the reminder system.

The second phase will involve interviewing guardians and healthcare professionals. These interviews have two foci. First, combined with patient, guardian, and/or household data from the randomized trial, these results will be used to develop a more comprehensive understanding of why pediatric patients attend appointments. The second focus is on improving the reminder system and developing new health technology interventions that can increase patient attendance.

研究类型

介入性

注册 (实际的)

263

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。

学习地点

      • Santiago、智利
        • Hospital Luis Calvo Mackenna

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

不超过 18年 (孩子、成人)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Guardian with a phone number (land-line or mobile) who is able to receive and answer voice calls
  • Guardian who is willing to take part in the study and complete the consent form
  • Guardian who is sufficiently proficient in Spanish so as to complete the questionnaire
  • Guardian's patient who has a referral appointment at Hospital Luis Calvo Mackenna who is 18 years of age or younger

Exclusion Criteria:

  • Guardian or child who do not meet the inclusion criteria
  • Anyone that lives in the same household as an enrolled study participant.

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:卫生服务研究
  • 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
无干预:No Intervention
The intervention arm subjects will not receive the automated interactive voice reminder before their appointment.
实验性的:Intervention
The intervention arm subjects will receive the automated interactive voice reminder before their appointment.
Health Call is an automated interactive voice reminder system that can contact guardians of patients ahead of their child's appointment, asks then confirms a security question about the patient, then, if the call recipient passes the security screen, provides a reminder about upcoming appointment.

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
Intervention impact
大体时间:9 months
Evaluate whether a patient reminder system, Health Call, can decrease the overall failure to attend appointment rate as a percentage of overall appointments
9 months
Key attendance factors
大体时间:9 months
Examine what demographic or health belief factors are significantly related to appointment attendance as measured by a psychometric questionnaire
9 months
Develop new interventions
大体时间:9 months
Investigate staff and recipient opinions of patient attendance, the Health Call system, and ideas for future interventions to reduce failure to attend as measured through in-depth interviews
9 months

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

  • 首席研究员:William Weiss, DrPH, MA、Johns Hopkins Bloomberg School of Public Health

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

2013年12月1日

初级完成 (实际的)

2016年1月1日

研究完成 (实际的)

2016年6月1日

研究注册日期

首次提交

2015年4月6日

首先提交符合 QC 标准的

2015年5月8日

首次发布 (估计)

2015年5月13日

研究记录更新

最后更新发布 (估计)

2016年6月14日

上次提交的符合 QC 标准的更新

2016年6月10日

最后验证

2015年5月1日

更多信息

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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