Exploring the inclusion of under-served groups in trials methodology research: an example from ethnic minority populations’ views on deferred consent

Effectiveness of participant recruitment strategies for critical care trials: A systematic review and narrative synthesis

(2021) Timia Raven-Gregg et al.   Clinical Trials

The Reporting of Race and Ethnicity in Medical and Science Journals

(2021) Annette Flanagin et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Examining the Inclusivity of US Trials of COVID-19 Treatment

(2021) Sukarn Chokkara et al.   JOURNAL OF GENERAL INTERNAL MEDICINE

Assessment of the Inclusion of Racial/Ethnic Minority, Female, and Older Individuals in Vaccine Clinical Trials

(2021) Laura E. Flores et al.   JAMA Network Open

Patient and Surrogate Postenrollment Perspectives on Research Using the Exception From Informed Consent: An Integrated Survey

(2020) Victoria M. Scicluna et al.   ANNALS OF EMERGENCY MEDICINE

The ethics of deferred consent in times of pandemics

(2020) Rieke van der Graaf et al.   NATURE MEDICINE

Developing a roadmap to improve trial delivery for under-served groups: results from a UK multi-stakeholder process

(2020) Miles D. Witham et al.   Trials

Addressing Health Disparities Among Minority Populations

(2020) Consuelo H. Wilkins et al.   JAMA Neurology

Informed consent procedures for emergency interventional research in patients with traumatic brain injury and ischaemic stroke

(2020) Erwin J O Kompanje et al.   LANCET NEUROLOGY

Protection by exclusion? The (lack of) inclusion of adults who lack capacity to consent to research in clinical trials in the UK

(2019) Victoria Shepherd et al.   Trials

Healthcare professionals’ understanding of the legislation governing research involving adults lacking mental capacity in England and Wales: a national survey

(2018) Victoria Shepherd et al.   JOURNAL OF MEDICAL ETHICS

Barriers to Clinical Trial Enrollment in Racial and Ethnic Minority Patients with Cancer

(2016) Lauren M. Hamel et al.   Cancer Control

Participant exclusion criteria in treatment research on neurological disorders: Are unrepresentative study samples problematic?

(2015) Ranak B. Trivedi et al.   Contemporary Clinical Trials

Patients’ Perspectives of Enrollment in Research Without Consent

(2015) Neal W. Dickert et al.   CRITICAL CARE MEDICINE

Key stakeholder perceptions about consent to participate in acute illness research: a rapid, systematic review to inform epi/pandemic research preparedness

(2015) Nina H. Gobat et al.   Trials

Research Recruitment Practices and Critically Ill Patients. A Multicenter, Cross-Sectional Study (The Consent Study)

(2013) Karen E. A. Burns et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Enrollment in research under exception from informed consent: The Patients’ Experiences in Emergency Research (PEER) study

(2013) Neal W. Dickert et al.   RESUSCITATION

Obtaining surrogate consent for a minimal-risk research study in the intensive care unit setting

(2012) Mary E Larkin et al.   Clinical Trials

Protecting Participants of Clinical Trials Conducted in the Intensive Care Unit

(2011) Brigid M. Flanagan et al.   JOURNAL OF INTENSIVE CARE MEDICINE

Challenges to Effective Research in Acute Trauma Resuscitation

(2010) John B. Holcomb et al.   SHOCK

Patients’ preferences for enrolment into critical-care trials

(2009) Damon C. Scales et al.   INTENSIVE CARE MEDICINE

Is the enrollment of racial and ethnic minorities in research in the emergency setting equitable?

(2009) Jeremy Sugarman et al.   RESUSCITATION

Patients' Views on Identifiability of Samples and Informed Consent for Genetic Research

(2008) Sara Chandros Hull et al.   AMERICAN JOURNAL OF BIOETHICS

Deferred proxy consent in emergency critical care research: Ethically valid and practically feasible

(2008) Tim C. Jansen et al.   CRITICAL CARE MEDICINE