Journal of Empirical Research on Human Research Ethics

Linking Survey and Twitter Data: Informed Consent, Disclosure, Security, and Archiving

The Psychological Risk of Minimal Risk Activities: A Pre- and Posttest Study Using the Self-Assessment Manikin

Inclusion of Marginalized Groups and Communities in Global Health Research Priority-Setting

Ethical Consistency and Experience: An Attempt to Influence Researcher Attitudes Toward Questionable Research Practices Through Reading Prompts

Concise Consent Forms Appreciated—Still Not Comprehended: Applying Revised Common Rule Guidelines in Online Studies

Dynamic Consent: An Evaluation and Reporting Framework

Researching Experiences of Cancer Risk Through Online Blogs: A Reflexive Account of Working Toward Ethical Practice

Reasoning “Uncharted Territory”: Notions of Expertise Within Ethics Review Panels Assessing Research Use of Social Media

Parents’ Perspectives on Decisions to Participate in Pediatric Clinical Research: Results From a Focus Group Study With Laypeople

Ethical Considerations in Using Social Media to Engage Research Participants: Perspectives of Australian Researchers and Ethics Committee Members

Measuring IRB Regulatory Compliance: Development, Testing, and Use of the National Cancer Institute StART Tool

A Decade of Empirical Research on Research Integrity: What Have We (Not) Looked At?

“Stop Talking to People; Talk with Them”: A Qualitative Study of Information Needs and Experiences Among Genetic Research Participants in Pakistan and Denmark

Trust in Centralized Large-Scale Data Repository: A Qualitative Analysis

Children in Social Research: Do Higher Payments Encourage Participation in Riskier Studies?

What Is “Publicly Available Data”? Exploring Blurred Public–Private Boundaries and Ethical Practices Through a Case Study on Instagram

The Contribution of Ethics Review to Protection of Human Participants: Comment on “Measuring the Quality and Performance of Institutional Review Boards”

Looking, But Not Listening? Theorizing the Practice and Ethics of Online Ethnography

Genomic Literacy and Awareness of Ethical Guidance for Genomic Research in Sub-Saharan Africa: How Prepared Are Biomedical Researchers?

Decades of Doing: Indigenous Women Academics Reflect on the Practices of Community-Based Health Research

Knowledge, Attitudes, and Practice Regarding Research Ethics Committees Among Health Care Faculty at Two Public Universities in Jordan

Interviewing a Person with Bipolar Disorder Under Involuntary Commitment: A Case Report

Commentary 2: Qualitative Research with Vulnerable Persons—How to Ensure that Burdens and Benefits are Proportional and Fairly Distributed

Commentary on “Measuring the Quality and Performance of Institutional Review Boards”

Commentary 1: Research with Persons Under Involuntary Commitment—Ethical Issues Surrounding Competence and Voluntariness

Attitudes Toward Genetics and Genetic Testing Among Participants in the Jackson and Framingham Heart Studies

From Moving Beyond Compliance to Quality to Moving Beyond Quality to Effectiveness: Realities and Challenges

Australian Mental Health Consumer and Carer Perspectives on Ethics in Adult Mental Health Research

Factors Associated With Payments to Research Participants: A Review of Sociobehavioral Studies at a Large Southern California Research University

Commentary 1: Weksler-Derri et al.’s “Ethical Challenges in Participatory Research with Autistic Adults in Israel”

Commentary 2: Empirical Interviews and Moral Engagement—Commentary on “Interviewers as Intruders? Ethical Explorations of Joint Family Interviews”

Do Researchers in Empirical Ethics Studies Have a Duty to Act Upon their Findings? Case Study in End-of-Life Decision Making

Commentary 1: The Role of Ethical Reflexivity in Conducting Ethically Challenging Qualitative Research

Commentary 1: Whose Voice Matters? Questioning Power Relations through the Lens of Feminist Ethics

Commentary 2: Therapeutic Mis-Estimation and Fulfilling the Obligation to Treat Research Subjects with Respect

“You Really Do Have to Know the Local Context”: IRB Administrators and Researchers on the Implications of the NIH Single IRB Mandate for Multisite Genomic Studies

Providing Incentives to Youth Participants in Research: A Literature Review

Interviewers as Intruders? Ethical Explorations of Joint Family Interviews

Commentary 1: Informed Consent of Research Participants: The Gap between Regulations and Reality

Commentary 2: Neither Ill will Nor a Deliberate Intention: What Focus Groups Say about Professional Practices in Hospitals

Commentary 1: Sharing and Responding to Day-to-Day Ethics Challenges in Health Research

Barriers and Facilitators to Obtaining Informed Consent in a Critical Care Pediatric Research Ward in Southern Malawi

The Issue of “Context”: Data, Culture, and Commercial Context in Social Media Ethics

Automating Dynamic Consent Decisions for the Processing of Social Media Data in Health Research

Stakeholder Requirements for an Ethical Framework to Sustain Multiple Research Projects in an Emerging Living Lab Involving Older Adults

Special Issue: Why Ethically Reflect on Empirical Studies in Empirical Ethics? Case Studies and Commentaries

A Formative Qualitative Study on the Acceptability of Deferred Consent in Adult Emergency Care Research in Malawi