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临床试验/NCT03834870
NCT03834870已完成早期 1 期

Virtual cOaching in Making Informed Choices on Elder Mistreatment Self-Disclosure (VOICES)

Yale University2 个研究点 分布在 1 个国家目标入组 1,012 人开始时间: 2020年7月20日最近更新:
适应症

试验速览

阶段
早期 1 期
状态
已完成
入组人数
1,012
试验地点
2
主要终点
Implementation in Terms of Participation

研究概览

简要总结

To develop an interactive tool to screen for Elder Mistreatment (EM) in the Emergency Department (ED) to promote self-disclosure.

详细描述

To develop and refine the interactive VOICES tool, which will promote self-identification and self-disclosure to increase reporting of EM at point-of-care in the Emergency Department (ED) setting. Prior to conducting a feasibility study, focus groups will be conducted to inform the process and to develop a tool to evaluate the use of VOICES.

Feasibility Study: To conduct a feasibility study (N= 800) examining the use of VOICES in a busy ED.

Exploratory Aim: To perform a preliminary evaluation of the accuracy of VOICES as a screening tool in correctly classifying EM cases that were referred to Adult Protective Services (APS).

研究设计

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

入排标准

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

入选标准

  • Age 60 years or older
  • Non-full trauma track
  • Alert and oriented to person and place
  • AMT-4 score of 4
  • Able to consent and communicate in English
  • Agrees and able to use the iPad
  • Not in police custody

排除标准

  • subjects who live in nursing homes or other long-term care sitting and do not reside in community setting
  • patients will be excluded if they cannot safely undergo the studies required for participation
  • subjects with clear signs of EM
  • Patient or clinician refusal to participate
  • severe hearing and vision impairment
  • presenting with active psychotic symptoms
  • presenting with acute intoxication
  • COVID-19 positive

结局指标

主要结局

Implementation in Terms of Participation

时间窗: up to 16 months

Participation will be determined by the ratio of participants who are successfully enrolled to the total number of eligible patients. The numerator, denominator, frequencies and 95% confidence intervals will be reported.

Implementation in Terms of Usage

时间窗: up to 16 months

Usage will be determined by the number of consented participants enrolled in the study who used VOICES to completion.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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