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临床试验/NCT02702284
NCT02702284已完成不适用

Advance Directives Completion Rates and an Intervention to Address Health Literacy in a Clinic Population

University of Florida4 个研究点 分布在 1 个国家目标入组 529 人开始时间: 2017年6月5日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
529
试验地点
4
主要终点
Presence of advance directive scanned into electronic medical record

研究概览

简要总结

The ability to communicate with patients is profoundly impacted by their health literacy - the ability to interpret documents, read and write prose, use quantitative information and speak and listen effectively. Limited health literacy is commonplace and associated with multiple poor health outcomes including frequent readmission's and high mortality. Advance directives are an important tool in respecting patient autonomy in health care interventions. Advance directives can also reduce health care costs by avoiding unwanted, unnecessary care at the end of life. At the University of Florida (UF) Health currently an initiative is underway to improve the delivery of advance directives to patients in the hospital as well as the outpatient clinics.

The aim of this research study is to enhance completion rates of advance directives by taking into consideration a patient's health literacy level. Specifically, the investigators plan to assess the impact of an ambulatory intervention on the completion rate of advance directives for patients with adequate and limited health literacy. The hypothesis is that both groups (adequate and limited health literacy) will benefit from the intervention, but patients with limited health literacy will show a greater improvement in the advance directives completion rate.

详细描述

The purpose of this research study is to improve completion of Advance Directives. These are documents that patients use to let doctors know what their wishes for treatment are and who they would want to make decisions for them if they could not make decisions for themselves.

At the time of the clinic visit to the Internal Medicine at Medical Plaza (IMMP) or the Internal Medicine at Tower Hill (IMTH) subjects will be invited to participate in the study.

Research Assistant(s) RA Responsibilities:

All Potential Study Subjects:

  1. RA will interview study subject in a private area (exam room or empty office).
  2. RA will assess eligibility criteria.
  3. RA will obtain informed consent.
  4. RA will randomize the subjects to either intervention or control.
  5. RA will explain to the subjects how to return the advance directive (AD)

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

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

入选标准

  • No advance directive in electronic medical record,
  • speaks English,
  • has intact cognitive function

排除标准

  • Age 50 or under,
  • already has an advance directive in electronic medical record,
  • does not speak English,
  • cognitive dysfunction

结局指标

主要结局

Presence of advance directive scanned into electronic medical record

时间窗: 6 months from enrollment

The research assistant will review the subject's electronic medical record for a copy of a signed advance directive.

次要结局

  • Number of reminder phone calls needed(6 months)
  • Client Evaluation of Services Questionnaire(day of study)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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