Imagen de Portada

Participant Misrepresentation in Online Focus Groups: Red Flags and Proactive Measures

Fuente: Wiley Open Access

Guardado en:

Detalles Bibliográficos
Autores principales:	Lesley Andrew, Emily Gizzarelli, Mohamed Estai, Ruth Wallace
Formato:	Artículo Open Access
Publicado:	Wiley 2024
Materias:	Ethics & Human Research
Acceso en línea:	Acceder al recurso
Etiquetas:	Agregar Etiqueta Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares

Mandating Evidence‐Based Informed Consent Practices: A Critical Engagement with IRB Leader Focus Group Findings
por: Meredith V. Parsons, et al.
Publicado: (2025)

Research Participant Bill of Rights: Clarifying the Role of Research Physicians
por: Mark A. Rothstein
Publicado: (2025)

Positive and Negative Social Consequences of Participating in a Sexual‐Network Study
por: Morgan Spahnie, et al.
Publicado: (2024)

Acceptability and Feasibility of Using Educational Incentives for Research Participation to Advance Antiracism
por: Barbara Green‐Ajufo, et al.
Publicado: (2025)

Perspectives of Information Access in the Informed Consent Process for Clinical Research Participation in Australia
por: Fleur O'Hare, et al.
Publicado: (2026)

Human Research Protection Training Requirements: Alternatives for Community Researchers at CTSA‐Funded Research Institutions
por: Emily E. Anderson, et al.
Publicado: (2025)

(Epistemic) Injustice and Resistance in Canadian Research Ethics Governance
por: Sarah Clairmont, et al.
Publicado: (2025)

Brain Organoid Research in a Post‐Dobbs World
por: Christine N. Coughlin, et al.
Publicado: (2025)

Bioethicists’ Perspectives on Ethical Research: Results of the “Views in Bioethics Survey”
por: Leah Pierson, et al.
Publicado: (2026)

Ethical Considerations for Enrolling “Invested Parties” in Large‐Scale Clinical Studies: Insights from the RECOVER Initiative
por: Kellie Owens, et al.
Publicado: (2024)

Human Research Protections during Emergencies: An Integrative Review
por: Lauren M. Sauer, et al.
Publicado: (2026)

Research with Refugee Populations in North America: Applying the NIH Guiding Principles for Ethical Research
por: Julie M. Aultman, et al.
Publicado: (2024)

The Ethical Case for Decentralized Clinical Trials
por: Kathryn Muyskens, et al.
Publicado: (2024)

Should Researchers Destroy Audio or Video Recordings?
por: David B. Resnik, et al.
Publicado: (2024)

Single IRB Review and Local Context Considerations: A Scoping Review
por: Stephanie R. Morain, et al.
Publicado: (2024)

Ethical Issues Faced by Data Monitoring Committees: Results from an Exploratory Qualitative Study
por: Seema K. Shah, et al.
Publicado: (2024)

Navigating University Openness in Research Policy Inconsistent with Indigenous Data Sovereignty: A Case Analysis
por: Molly Wick, et al.
Publicado: (2024)

Moving to the Middle Ground: Redefining Genomic Utility to Expand Understanding of Familial Benefit
por: Kyle B. Brothers, et al.
Publicado: (2024)

Rapid Review of Therapy Protocols for Public Health Emergencies
por: Bruce G. Gordon, et al.
Publicado: (2024)

Should Children Be Included in Human Challenge Studies?
por: Ariella Binik
Publicado: (2024)

The European Health Data Space as a Case Study
por: Edward S. Dove
Publicado: (2024)

Ethics in Mental Health Research with Haitian Migrants: Lessons from a Community‐Based Study in Santiago, Chile
por: Francesca McLaren, et al.
Publicado: (2024)

Translational Bioethical Decision‐Making: Human Brain Organoids as a Case Study
por: John H. Evans
Publicado: (2024)

Translational Bioethics in China: Brain‐Computer Interface Research as a Case Study
por: Haidan Chen
Publicado: (2024)

Issue Information
Publicado: (2024)

The First‐ and Second‐Order Ethical Reasons Approach: The Case of Human Challenge Trials
por: Davide Battisti, et al.
Publicado: (2024)

The Prospect of Artificial Intelligence‐Supported Ethics Review
por: Philip J. Nickel
Publicado: (2024)

Exception from Informed Consent in Emergency Care Research: Reports from a Workshop Addressing “Edge Cases”
por: Jeremy Brown, et al.
Publicado: (2025)

Emergency Care Research and Exception from Informed Consent: Addressing the Spectrum of Capacity for Consent
por: Neal W. Dickert, et al.
Publicado: (2026)

Expectations, Tensions, and Brokerage: A Discourse Analysis of Community Engagement with Health Research in South Africa
por: Sonja Klingberg, et al.
Publicado: (2025)

Issue Information
Publicado: (2025)

Issue Information
Publicado: (2025)

Navigating Challenges with IRB Review for Community‐Engaged Research with Transgender Youth in the United States
por: Alic G. Shook, et al.
Publicado: (2025)

Stakeholder Views on Novel Consent Forms for an Acute Stroke Trial
por: Candace D. Speight, et al.
Publicado: (2025)

Our Theater of Anonymity
por: Sara Meeder, et al.
Publicado: (2025)

What's in a Lie? How Researchers Judge the Justifiability of Deception
por: Kamiel Verbeke, et al.
Publicado: (2025)

Engaging Sub‐Saharan African Migrants in Social and Health Studies in Australia: Research and Ethical Challenges
por: Andre M. N. Renzaho, et al.
Publicado: (2025)

Digital Twins in Translational Research and Health Care: An Anthropological Perspective
por: Jennifer K. Wagner
Publicado: (2026)

Equitable Data Sharing in Collaborative Health Research in Sub‐Saharan Africa: A Translational Bioethics Perspective
por: Pamela Andanda, et al.
Publicado: (2025)

Natural Language Processing in Clinical Research Recruitment: A Scoping Review Enriched with Stakeholder Insights
por: Lara Bernasconi, et al.
Publicado: (2025)