The Role of Inclusion Benefits in Ethics Committee Assessment of Research Studies
Year: 2019
Type: article
Abstract: The relationship between risks and benefits is central to the ethics of research involving human participants. Traditionally, to be ethically justifiable, risks should be reasonable in relation to anticipated benefits (if any) to subjects and to the potential social benefits resulting from research. This calculus is being further complicated by findings from an increasing number of social science studies that reveal that prospective and actual research participants frequently describe various types of inclusion benefits (for example, personal benefits such as access to or improved health care, increased knowledge about their disease or condition, and greater solidarity with the local community) as important to them. What is the ethical significance of such inclusion benefits, particularly those nonmedical in nature, for research ethics committees' risk-benefit assessment of research studies? We argue that, unless participants are clearly mistaken in their perceptions, ethics committees should take these types of inclusion benefits into account, and we suggest a few ways this might look in practice.
Source: Ethics & Human Research
DOI: 10.1002/eahr.500015
Language: English
Topic: Ethics in Clinical Research
Field: Medicine
Domain: Health Sciences
Open Access status: green
Awards: G2720746427, Ethics of HIV-Related Research Involving Adolescents in Kenya, Unintended and Intended Implications of HIV Cure: A Social and Ethical Analysis, Acute Infection: Lived Experiences and Ethical Challenges in HIV Research, Integrating Decision Making Studies into HIV Cure Trials: A real-time longitudinal assessment
OpenAlex ID: W2945688055
