跳至主要内容
临床试验/NCT03419832
NCT03419832已完成不适用

The NEAT Study: An Examination of a Novel Consent Form Design in a Real-world Setting

Wake Forest University Health Sciences2 个研究点 分布在 1 个国家目标入组 101 人开始时间: 2017年4月4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
101
试验地点
2
主要终点
Comprehension of the NEAT Form

研究概览

简要总结

There is evidence that the current design and content provided by most biomedical research informed consent documents do not consistently meet the expectations researchers place on them to effectively inform research participants of information thought to be most important in facilitating their ability to make informed decisions about participation. The need for revisions to the informed consent document design is supported by empirical research.This pilot study will examine the effectiveness of the New Executive and Appendix Template (NEAT) form when used in the consent process for individuals participating in the Atherosclerosis Risk in Communities (ARIC) Neurocognitive Study.

详细描述

The importance of informed consent is to ensure that participants in clinical research are provided the opportunity to make autonomous choices is a paramount ethical premise in human research. The effectiveness of consent document design and consent process to accurately and fully convey the elements of informed consent is critical and deserves further study. Development of an improved informed consent document design for clinical studies would be a valuable contribution to human research. Chunking sentences or phrases in text into related groupings resulted in a positive significant improvement in reading comprehension among students with poor reading skills. Because the information contained in consent documents can be complex, detailed, and novel for potential research participants, the use of a modified form of chunking may be an effective and a low cost way of improving comprehension of the elements of consent. Specifically, the primary objective of the study is to determine if participants who receive the NEAT form report greater comprehension at the end of the consent process, than participants who receive a standard form.

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
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Individuals who are eligible for the ARIC study, with which this pilot study is cooperating.

排除标准

  • Any individuals not eligible for the ARIC study.

结局指标

主要结局

Comprehension of the NEAT Form

时间窗: at visit one, up to 24 hours

Following the consent process, participants will be administered the Comprehension tool to measure their comprehension. The summary scores will be used to address the primary aim of whether or not the NEAT consent form improves participant comprehension. There are 7 questions, each question is rated 0-2 with a total scale of 0-14. Higher values denotes better outcomes.

次要结局

  • Qualitative Analysis of the Readability and Understandability of the Consent Form by Participants(at visit one, up to 24 hours)
  • Qualitative Analysis of the Format and Design of the Consent Form by Participants(at visit one, up to 24 hours)
  • Qualitative Analysis of the Time of Discussion of the Consent Form by Participants(at visit one, up to 24 hours)
  • Qualitative Analysis of the Format and Design of the Consent Form by Study Team(at visit one, up to 24 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验

The New Executive and Appendix Template (NEAT) Study | 临床试验