Pilot label comprehension study for an over-the-counter combined oral contraceptive pill in the United States.

IF 3.4 2区 医学 Q1 DEMOGRAPHY
Kate Grindlay, Katherine Key, Russell D Bradford, Chiara Amato, Kelly Blanchard, Daniel Grossman
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引用次数: 1

Abstract

Context: A growing body of evidence supports over-the-counter access to oral contraceptives in the United States. An important consideration for over-the-counter approval is consumers' ability to understand key package label messages related to safety and effectiveness without clinician involvement. We developed a prototype over-the-counter Drug Facts Label for a combined oral contraceptive pill and conducted a pilot label comprehension study to evaluate consumer understanding of key messages for use.

Methods: In November-December 2020, we conducted interviews with 163 adults and teens in the United States who were aged 12-49 years and identified as female or another gender but had a uterus and the ability to become pregnant. We developed 11 primary endpoints based on assessment of clinical risks that could occur if consumers fail to heed them, including messages about contraindications and directions for use; 11 secondary endpoints represented additional important information but with lower potential for clinical consequences if not understood. We evaluated endpoint comprehension by computing frequencies, percentages, and 2-sided Exact (Clopper-Pearson) 95% confidence intervals for observed proportions.

Results: Ten of the 11 primary endpoints and 10 of the 11 secondary endpoints were each understood by ≥95% of participants. The remaining primary endpoint on use with prior blood clots was understood by 89% of participants. The remaining secondary endpoint on the product being designed for "people who have the ability to become pregnant" was understood by 83% of participants.

Conclusion: Participants understood the key label information required for safe and effective combined oral contraceptive use without clinician involvement.

美国一种非处方联合口服避孕药的试点标签理解研究。
背景:在美国,越来越多的证据支持非处方获得口服避孕药。非处方药批准的一个重要考虑因素是消费者在没有临床医生参与的情况下理解与安全性和有效性相关的关键包装标签信息的能力。我们为联合口服避孕药开发了一种非处方药事实标签原型,并进行了一项试点标签理解研究,以评估消费者对使用关键信息的理解。方法:在2020年11月至12月期间,我们对163名美国成年人和青少年进行了访谈,他们年龄在12-49岁之间,被确定为女性或其他性别,但有子宫和怀孕能力。我们根据临床风险评估制定了11个主要终点,这些风险可能发生在消费者不注意的情况下,包括关于禁忌症和使用说明的信息;11个次要终点代表了额外的重要信息,但如果不了解,临床后果的可能性较低。我们通过计算频率、百分比和观察到的比例的双侧精确(Clopper-Pearson) 95%置信区间来评估终点理解。结果:11个主要终点中的10个和11个次要终点中的10个均被≥95%的参与者理解。剩余的主要终点对于既往血凝块的使用,89%的参与者理解。该产品的其余次要终点是为“有能力怀孕的人”设计的,83%的参与者理解。结论:在没有临床医生参与的情况下,参与者了解安全有效地使用联合口服避孕药所需的关键标签信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.10
自引率
3.40%
发文量
24
期刊介绍: Perspectives on Sexual and Reproductive Health provides the latest peer-reviewed, policy-relevant research and analysis on sexual and reproductive health and rights in the United States and other developed countries. For more than four decades, Perspectives has offered unique insights into how reproductive health issues relate to one another; how they are affected by policies and programs; and their implications for individuals and societies. Published four times a year, Perspectives on Sexual and Reproductive Health includes original research, special reports and commentaries on the latest developments in the field of sexual and reproductive health, as well as staff-written summaries of recent findings in the field.
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