Informed Consent Monitoring
Informed Consent Monitoring is a methodological framework within trial monitoring that systematically verifies the authenticity, comprehension, and voluntariness of participants' consent in clinical or research trials to ensure ethical and regulatory compliance.
30
Publications
876
Citations
144
Authors
96
Institutions
Publications per year
2017–2026
5
Parents
30
Evaluating the quality of informed consent
Jeremy Sugarman, Philip W. Lavori, Maryann Boeger et al. · Clinical Trials · 2005 · 144 citations
Monitoring clinical research: an obligation unfulfilled.
Charles Weijer, Stan Shapiro, A Fuks et al. · PubMed · 1995 · 55 citations
Public Health, Health Policy, Clinical Research Regulation +16
Adil E. Bharucha, Cathi T. Rhodes, Christine M Boos et al. · Mayo Clinic Proceedings · 2021 · 42 citations · Full text
Conversion Disorder- Mind versus Body: A Review.
PubMed · 2015 · 38 citations
Pharmacy, Neurology, Medical Ethics +16
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96

Johns Hopkins University
Baltimore, United States
4 h-index
20 publications
545 citations
Stanford University
Stanford, United States
3 h-index
3 publications
178 citations
The University of Texas Southwestern Medical Center
Dallas, United States
2 h-index
2 publications
36 citations
Johns Hopkins Berman Institute of Bioethics
Baltimore, United States
2 h-index
2 publications
157 citations

University of Toronto
Toronto, Canada
2 h-index
4 publications
92 citations
Assistance Publique – Hôpitaux de Paris
Paris, France
1 h-index
7 publications
70 citations

Nantes Université
Nantes, France
1 h-index
1 publications
10 citations
Post Graduate Institute of Medical Education and Research
Chandigarh, India
1 h-index
8 publications
96 citations
1–8 of 96
Repository · 2 publications · 93 citations
2
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2 publications · 157 citations
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2 publications · 64 citations
2
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2 publications · 32 citations
2
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1 publications · 15 citations
1
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1–5