跳至主要内容
临床试验/NCT07122960
NCT07122960进行中(未招募)不适用

Strengthening Informed Consent for Authentic Participation in Perinatal HIV Research

Columbia University1 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2024年9月2日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
58
试验地点
1
主要终点
Summed score from the validated Quality of Informed Consent (QUIC) instrument.

研究概览

简要总结

This study evaluates a visual Informed Consent Form (ICF) compared to a standard, text-only ICF as an approach to achieving meaningful consent into a clinical trial. The visual ICF uses cartoon characters, graphics and easy-to-understand text to cover the full content of a standard, text-only ICF. In this study, women who are considering enrollment into a clinical trial of a nutrition intervention for their infants will be randomized to either the visual ICF or to the text-only ICF. Qualitative and quantitative data will be collected immediately after the consent process and 8 weeks later. In addition, women not eligible for enrollment into the infant nutrition trial will be asked questions about their opinions regarding the visual ICF. The overall goal of the sub-study is to inform efforts to improve meaningful consent into clinical trials by evaluating whether the visual ICF improves understanding of the trial.

详细描述

The overall goal of the study is to inform efforts to improve meaningful consent into clinical trials. The investigators are evaluating whether substituting a visual informed consent form (ICF) for the usual text-only ICF will increase potential participants' understanding of the risks and benefits of research and contribute to more informed participation.

This study is nested within a larger clinical trial of a nutrition intervention for infants underway in South Africa. For this larger trial, a visual ICF was developed that covers the identical content of a standard text-only ICF. For this sub-study (n=40), women who are considering enrollment into this larger study who agree to enroll in the sub-study, will be randomized to either receive the visual ICF or to receive the text-only ICF. Following the decision to either participate or not in the larger trial, women will be interviewed about their knowledge recall of the content of the ICF including concerning the trial goal, the voluntary nature of participation, potential benefits, potential risks, and randomization measured using a mix of true/false/uncertain and likert-type response options. Questions will also be asked about decision conflict, self-rated understanding, self-efficacy, and satisfaction with the informed consent process. Eight weeks later, at one of the follow-up visits in the larger trial, these questions will be repeated to determine knowledge retention and decision regret and trust in the study team. The evaluation includes both quantitative and qualitative data which will be analyzed using standard mixed methods analysis techniques.

In addition, an independent population of women from the same area with infants of the same age but who are not eligible for the larger trial will be enrolled (n=20). For this population, participating in the trial is a hypothetical situation and thus respondents have no direct connection with the study team and thus are less prone to positive bias in responses. Questions will be asked concerning opinions about the visual ICF using a semi-structured, qualitative, think-aloud approach.

研究设计

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

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Women ages 18-45 years of age
  • •Pregnant women or women that have recently given birth within the past 2-6 weeks

排除标准

  • •Unwilling to provide consent
  • •Severe maternal or infant illness (e.g. tuberculosis, major psychiatric or neurological conditions)
  • •Inability to communicate in one of the three languages (English, isiXhosa, or Afrikaans)

研究组 & 干预措施

Visual Informed Consent Form (ICF)

Experimental

干预措施: Visual ICF (Other)

Text-only Informed Consent Form

Active Comparator

干预措施: Text-only ICF (Other)

结局指标

主要结局

Summed score from the validated Quality of Informed Consent (QUIC) instrument.

时间窗: Immediately after the consent process (Day 0) and 8 weeks later

The QUIC measures knowledge recall. The summed score of 10 knowledge items comprising key concepts of informed consent will be calculated. The scores range between 0 and 22 with higher scores indicating higher knowledge.

次要结局

  • Decision Regret Scale(8 weeks after consent process)
  • Self-rated Understanding(Immediately after consent process (Day 0))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Louise Kuhn

Professor of Epidemiology

Columbia University

研究点 (1)

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