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Paying Research Participants: Regulatory Uncertainty, Conceptual Confusion, and a Path Forward.

TLDR
It is argued that the default should be changed to favor, rather than encourage suspicion of, offers of payment to research participants, and that rejection of research exceptionalism with respect to payment helps settle open debates about how best to define coercion and undue influence.
Abstract
The practice of offering payment to individuals in exchange for their participation in clinical research is widespread and longstanding. Nevertheless, such payment remains the source of substantial debate, in particular about whether or the extent to which offers of payment coerce and/or unduly induce individuals to participate. Yet, the various laws, regulations, and ethical guidelines that govern the conduct of human subjects research offer relatively little in the way of specific guidance regarding what makes a payment offer ethically acceptable-or not. Moreover, there is a lack of definitional agreement regarding what the terms coercion and undue inducement mean in the human subjects research context. It is, therefore, unsurprising that investigators and Institutional Review Boards (IRBs) experience confusion about how to evaluate offers of payment, and lean toward conservative approaches. These trends are exemplified by our pilot data regarding the ways in which some IRB members and investigators (mis)understand the concepts of coercion and undue inducement, as well as the ways in which certain research institutions oversee offers of payment at a local level. This article systematically examines the legal and ethical dimensions of offering payment to research participants. It argues that many concerns about offers of payment to research participants can be attributed to the misguided view that such offers ought to be treated differently than offers of payment in other contexts, a form of "research exceptionalism." We show that rejection of research exceptionalism with respect to payment helps settle open debates about both how best to define coercion and undue influence, and how to understand the relation between these concepts and offers of payment. We argue for adoption of our preferred definitions, ideally by regulatory authorities, and against the conventional conservatism toward payment of research participants. Instead, we draw attention to the rarely asked, even radical, question: are research participants paid enough? We conclude by arguing that we ought to change the default to favor, rather than encourage suspicion of, offers of payment to research participants.

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Citations
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The Gift Relationship: From Human Blood to Social Policy

Frances K. Widmann
- 07 Jun 1971 - 
TL;DR: Professor Titmuss, an eminent English social theorist, believes that man is inherently altruistic and that the duty of government is to create that social and economic climate which best channels man's drive to work together for the common good.
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A Framework for Ethical Payment to Research Participants

TL;DR: Ethical Payment to Research Participants The authors propose a framework for evaluating the appropriateness of payments to research participants and distinguish three acceptable rationales for these payments.
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TL;DR: Key ethical and methodological considerations in the design and implementation of qualitative research in the COVID-19 era and in pivoting to virtual methods are discussed, including internet-based archival research and netnography, including social media; participatory video methods, including photo elicitation and digital storytelling.
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Recruitment of caregivers into health services research: lessons from a user-centred design study

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References
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Book ChapterDOI

World Medical Association Declaration of Helsinki: Ethical Principles for Medical Research Involving Human Subjects

TL;DR: Comparing the socialist nature of many European counties, there is a requirement that provision be made for patients to be made whole regardless of the outcomes of the trial or if they happened to have been randomized to a control group that did not enjoy the benefits of a successful experimental intervention.
Journal ArticleDOI

What Makes Clinical Research Ethical

TL;DR: 7 requirements are proposed that systematically elucidate a coherent framework for evaluating the ethics of clinical research studies and are universal, although they must be adapted to the health, economic, cultural, and technological conditions in which clinical research is conducted.
Journal ArticleDOI

The Gift Relationship: From Human Blood to Social Policy

Frances K. Widmann
- 07 Jun 1971 - 
TL;DR: Professor Titmuss, an eminent English social theorist, believes that man is inherently altruistic and that the duty of government is to create that social and economic climate which best channels man's drive to work together for the common good.
Journal ArticleDOI

Eligibility criteria of randomized controlled trials published in high-impact general medical journals: a systematic sampling review.

TL;DR: The RCTs published in major medical journals do not always clearly report exclusion criteria and justification for exclusions related to concomitant medication use, medical comorbidities, female sex, and socioeconomic status were more likely to be poorly justified.
Journal ArticleDOI

Quality of informed consent in cancer clinical trials: a cross-sectional survey

TL;DR: In multivariate analysis, increased knowledge was associated with college education, speaking only English at home, use of the US National Cancer Institute consent form template, not signing the consent form at initial discussion, presence of a nurse, and careful reading of the consent forms.
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