Sage Journals: Discover world-class research

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Research article

First published 2018-7

Assessment of Parents’/Guardians’ Initial Comprehension and 1-Day Recall of Elements of Informed Consent Within a Mozambican Study of Pediatric Bacteremia

Ezequiel B. Ossemane, Troy D. Moon, Jahit Sacarlal [...]

Journal of Empirical Research on Human Research Ethics

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Research article

First published 2022-10

Understanding of Critical Elements of Informed Consent in Genomic Research: A Case of a Paediatric HIV-TB Research Project in Uganda

Francis Anyaka Amayoa, Frederick Nelson Nakwagala, John Barugahare [...]

Journal of Empirical Research on Human Research Ethics

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Research article

First published 2025-7

Content and Readability of Informed Consent Documents Approved by Research Ethics Committees of Health Institutions in South-East Nigeria

Onyinye Chime, Emmanuel Ezeome

Journal of Empirical Research on Human Research Ethics

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Research article

First published 2016-6

Informed Consent Should Be a Required Element for Newborn Screening,Even for Disorders with High Benefit-Risk Ratios

Norman Fost

The Journal of Law,Medicine & Ethics

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Research article

First published 2011-1

Interventions to Improve Patient Comprehension in Informed Consent for Medical and Surgical Procedures

Yael Schenker, Alicia Fernandez, Rebecca Sudore [...]

Medical Decision Making

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Research article

First published 2021-7

Informed Consent for Online Research—Is Anybody Reading?: Assessing Comprehension and Individual Differences in Readings of Digital Consent Forms

Caitlin Geier, Robyn B. Adams, Katharine M. Mitchell [...]

Journal of Empirical Research on Human Research Ethics

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Research article

First published 2020-10

Informing Informed Consent for HIV Research

Laura M. Campbell, Emily W. Paolillo, Robert Bryan [...]

Journal of Empirical Research on Human Research Ethics

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Research article

First published 2023-10

Regulatory compliance and readability of informed consent forms in industry-sponsored drug development clinical trials

Nahathai Dukaew, Mingkwan Na Takuathung, Wannachai Sakuludomkan [...]

Clinical Trials

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Other

First published 2004-10

The Problem of Readability of Informed Consent Documents for Clinical Trials of Investigational Drugs and Devices: United States Considerations

S. Michael Sharp

Therapeutic Innovation & Regulatory Science

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Research article

First published 1980-1

Legal and Ethical Issues in Clinical Pharmacy Research — Informed Consent,Part I

Dev S. Pathak, Thomas S. Foster, Cynthia L. Raehl

Annals of Pharmacotherapy

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