Quality of informed consent in cancer clinical trials
A cross-sectional survey
Bibliographic Data
| ID | 23319009 |
|---|---|
| Authors | Steven Joffe (0000-0002-0667-7384, Boston Children's Hospital), E Francis Cook (Brigham and Women's Hospital), Paul D Cleary (0000-0001-7527-4354, Harvard University), Jeffrey W Clark (0000-0001-9524-3600, Massachusetts General Hospital), Jane C Weeks (Brigham and Women's Hospital, corresponding author) |
| Year | 2001 |
| Volume | 358 |
| Issue | 9295 |
| Pages | 1772-1777 |
| Publication date | 2001-11-01 |
| Peer Reviewed | Yes |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | The Lancet (JOURNAL) |
| Journal identifiers | ISSN: 0099-5355 • E-ISSN: 0140-6736 |
| Publisher | Elsevier BV (PUBLISHER) |
| DOI | 10.1016/s0140-6736(01)06805-2 |
| PMID | 11734235 |
| OpenAlex | W1964708144 |
| Language | EN |
| Citations received | 65 |
| References cited | 21 |
Alternative medicine · Clinical trial · Cross-sectional study · Family medicine · Informed consent · MEDLINE · Pathology · Ethics in Clinical Research · Medicine · Mental Health and Patient Involvement · Patient-Provider Communication in Healthcare
‘A No‐Brainer, but Not a Simple Decision’
Competency of legal subjects in informed consent as a standard agreement
Filling in informed consent in the c-section operations section of Subang Regional General Hospital
Is Informed Consent for Extracorporeal Life Support Even Possible
Is Informed Consent for Extracorporeal Life Support Even Possible
How Should a Research Ethicist Combat False Beliefs and Therapeutic Misconception Risk in Biomedical Research
Views of the Process and Content of Ethical Reviews of Hiv Vaccine Trials Among Members of Us Institutional Review Boards and South African Research Ethics Committees
Consent for participating in clinical trials ‐ Is it really informed
Motivations, Understanding, and Voluntariness in International Randomized Trials
The Quality of Informed Consent in a Clinical Research Study in Thailand
Misunderstanding in Clinical Research
Interventions to Improve Research Participants' Understanding in Informed Consent for Research
Parental and professional perceptions of informed consent and participation in a time-critical neonatal trial
Reshaping the review of consent so we might improve participant choice
Reshaping consent so we might improve participant choice (III) – How is the research participant’s understanding currently checked and how might we improve this process
Dynamic consent
Informed Consent, Biobank Research, and Locality
Methods and Practices of Investigators for Determining Participants' Decisional Capacity and Comprehension of Protocols
Participants’ Understanding of Informed Consent in a Randomized Controlled Trial for Chronic Knee Pain
Understanding the Use of Optimal Formatting and Plain Language When Presenting Key Information in Clinical Trials
Participants' Recall and Understanding of Genomic Research and Large-Scale Data Sharing
Purpose and Benefits of Early Phase Cancer Trials
Phase 3 Oncology Clinical Trials in South Africa
A Randomized Controlled Trial of an Electronic Informed Consent Process
Parents' Online Portrayals of Pediatric Treatment and Research Options
Benefits and Burdens of Participation in a Longitudinal Clinical Trial
Education Level, Primary Language, and Comprehension of the Informed Consent Process
Informed Consent and Genomic Incidental Findings
An Analysis of Informed Consent Form Readability of Oncology Research Protocols
Readability of Informed Consent Documents (1987–2007) for Clinical Trials
Are Well-Informed Potential Trial Participants More Likely to Participate
Perspectives on Human Microbiome Research Ethics
Using Formative Research to Develop a Context-Specific Approach to Informed Consent for Clinical Trials
Analysis of the Status of Subject Recruitment in Clinical Trials in Shandong, China
Improving Informed Consent with Minority Participants
Participants’ Accounts on Their Decision to Join a Cohort Study With an Attached Biobank
Towarda Construct Definition of Informed Consent Comprehension
Reflexivity and the clinician-researcher
Randomisation before consent
Random Assignment and Informed Consent
Perfil e vozes dos participantes de pesquisas clínicas no Brasil
Relational Autonomy as a Theoretical Lens for Qualitative Health Research
Do High-Risk Young Adults Use the HIV Self-Test Appropriately? Observations from a Think-Aloud Study
Improving Participant Understanding of Informed Consent in an HIV-Prevention Clinical Trial
The many meanings of care in clinical research
Perceived Quality of Informed Refusal Process
Opinions of Researchers Based in the Uk on Recruiting Subjects From Developing Countries Into Randomized Controlled Trials
Improving informed consent
Development and evaluation of a web-based assent for adolescents considering an HIV vaccine trial
Pilot study demonstrating effectiveness of targeted education to improve informed consent understanding in Aids clinical trials
Ethical Issues in Conducting Research With Deaf Populations
Quality of Parental Consent in a Ugandan Malaria Study
Teatro na educação de crianças e adolescentes participantes de ensaio clínico
Enrolling Decisionally Impaired Adults in Clinical Research
L'individu dans un essai thérapeutique
Ignorance as an under-identified social problem1
Conhecimento e voluntariedade para participação em pesquisas
Clinical trials as treatment option
Enquête sur les pratiques d'information et de recueil du consentement dans la recherche biomédicale
Understanding of informed consent in a low-income setting
Therapeutic misconception and the appreciation of risks in clinical trials
Conflicting notions of research ethics
Therapeutic misconception in early phase gene transfer trials
Trust and informed consent
Toward Personalized Informed Consent in Cancer Care
| Unique citing works | 65 |
|---|---|
| Citations per year | 2,71 |
| Citation span | 2002 - 2026 (25) |
| Citation velocity | current |
| Highly cited | No |
| Citation types | Neutral: 54 |