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不同健康素养水平女性对参与临床试验的看法。

Perceptions of Clinical Trial Participation Among Women of Varying Health Literacy Levels.

机构信息

Duke University Health System.

University of Virginia.

出版信息

Oncol Nurs Forum. 2020 May 1;47(3):273-280. doi: 10.1188/20.ONF.273-280.

Abstract

PURPOSE

To understand the perceptions of risk, benefit, and the informed consent process after enrolling in and completing a phase 2 clinical trial using intraoperative radiation therapy (IORT) for early-stage breast cancer, and to determine how perceptions varied based on women's health literacy levels.

PARTICIPANTS & SETTING: 20 participants who had already completed a phase 2 IORT clinical trial for early-stage breast cancer at an academic medical center.

METHODOLOGIC APPROACH

A qualitative descriptive study was conducted using structured interviews consisting of questions aimed to elicit responses from participants regarding experiences of informed consent and the research process. A validated brief health literacy questionnaire was used to determine health literacy levels of participants. The authors analyzed themes using inductive thematic analysis.

FINDINGS

Women with lower levels of health literacy reported feeling confident enough in the provider to make the decision to enroll in the clinical trial during the initial consultation, and, in general, women reported relying heavily on provider recommendation for enrolling in the clinical trial.

IMPLICATIONS FOR NURSING

Tailored approaches for patients with limited health literacy are needed during the clinical trial consent process. Additional longitudinal research with a larger sample size can extend study results and provide insight into the most effective way to modify the informed consent process for patients with limited health literacy.

摘要

目的

了解参与并完成使用术中放射治疗(IORT)治疗早期乳腺癌的 2 期临床试验后,对风险、获益和知情同意过程的认知,并确定这些认知如何因女性健康素养水平的不同而有所差异。

参与者和设置

20 名参与者已在学术医疗中心完成了早期乳腺癌的 2 期 IORT 临床试验。

方法学方法

采用结构访谈进行定性描述性研究,访谈包含旨在从参与者那里获得有关知情同意和研究过程体验的回答的问题。使用经过验证的简短健康素养问卷来确定参与者的健康素养水平。作者使用归纳主题分析来分析主题。

发现

健康素养水平较低的女性在最初的咨询中表示对提供者有足够的信心来做出参与临床试验的决定,并且总体而言,女性报告在很大程度上依赖提供者的建议来参与临床试验。

对护理的启示

在临床试验同意过程中,需要为健康素养有限的患者提供量身定制的方法。对更大样本量的患者进行更多的纵向研究可以扩展研究结果,并深入了解如何为健康素养有限的患者修改知情同意过程的最有效方法。

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