8 found
Order:
Disambiguations
Clement A. Adebamowo [5]Clement Adebamowo [3]
  1.  62
    Voluntary Participation and Comprehension of Informed Consent in a Genetic Epidemiological Study of Breast Cancer in Nigeria.Patricia A. Marshall, Clement A. Adebamowo, Adebowale A. Adeyemo, Temidayo O. Ogundiran, Teri Strenski, Jie Zhou & Charles N. Rotimi - 2014 - BMC Medical Ethics 15 (1):38.
    Studies on informed consent to medical research conducted in low or middle-income settings have increased, including empirical investigations of consent to genetic research. We investigated voluntary participation and comprehension of informed consent among women involved in a genetic epidemiological study on breast cancer in an urban setting of Nigeria comparing women in the case and control groups.
    Direct download (7 more)  
     
    Export citation  
     
    Bookmark   11 citations  
  2. Development and Pilot Testing of an Online Module for Ethics Education Based on the Nigerian National Code for Health Research Ethics.Olubunmi A. Ogunrin, Temidayo O. Ogundiran & Clement Adebamowo - 2013 - BMC Medical Ethics 14 (1):1-.
    Background: The formulation and implementation of national ethical regulations to protect research participants is fundamental to ethical conduct of research. Ethics education and capacity are inadequate in developing African countries. This study was designed to develop a module for online training in research ethics based on the Nigerian National Code of Health Research Ethics and assess its ease of use and reliability among biomedical researchers in Nigeria.MethodologyThis was a three-phased evaluation study. Phase one involved development of an online training module (...)
    Direct download (15 more)  
     
    Export citation  
     
    Bookmark   8 citations  
  3.  37
    Qualitative Study of Knowledge and Attitudes to Biobanking Among Lay Persons in Nigeria.Michael A. Igbe & Clement A. Adebamowo - 2012 - BMC Medical Ethics 13 (1):27-.
    Background Interest in biobanking for collection of specimens for non-communicable diseases research has grown in recent times. This paper explores the perspectives of Nigerians on donation of specimen for the biobanking research. Methods We conducted 16 Focus Group Discussions (FGD) with individuals from different ethnic, age and socio-economic groups in Kano (North), Enugu (Southeast), Oyo States (Southwest) and Abuja, the Federal Capital Territory (Central) of Nigeria. We used topic guides and prompt statements to explore the knowledge and understanding of interviewees (...)
    Direct download (10 more)  
     
    Export citation  
     
    Bookmark   11 citations  
  4.  36
    Paper: Surgeons' Opinions and Practice of Informed Consent in Nigeria.Temidayo O. Ogundiran & Clement A. Adebamowo - 2010 - Journal of Medical Ethics 36 (12):741-745.
    Background Informed consent is perhaps more relevant to surgical specialties than to other clinical disciplines. Fundamental to this concept is the provision of relevant information for the patient to make an informed choice about a surgical intervention. The opinions of surgeons in Nigeria about informed consent in their practice were surveyed. Methods A cross-sectional survey of surgeons in Nigeria was undertaken in 2004/5 using self-administered semistructured questionnaires. Results There were 102 respondents, 85.3% of whom were men and 58.8% were aged (...)
    Direct download (9 more)  
     
    Export citation  
     
    Bookmark   4 citations  
  5.  61
    Medical Ethics Education: A Survey of Opinion of Medical Students in a Nigerian University. [REVIEW]Clement A. Adebamowo - 2010 - Journal of Academic Ethics 8 (2):85-93.
    In Nigeria, medical education remains focused on the traditional clinical and basic medical science components, leaving students to develop moral attitudes passively through observation and intuition. In order to ascertain the adequacy of this method of moral formations, we studied the opinions of medical students in a Nigerian university towards medical ethics training. Self administered semi-structured questionnaires were completed by final year medical students of the College of Medicine, University of Ibadan, Nigeria. There were 82 (64.1%) male and 44 (34.4%) (...)
    Direct download (4 more)  
     
    Export citation  
     
    Bookmark   3 citations  
  6.  17
    Consensus Standards for Introductory E-Learning Courses in Human Participants Research Ethics.John Williams, Dominique Sprumont, Marie Hirtle, Clement Adebamowo & Paul Braunschweiger - 2014 - Journal of Medical Ethics 40 (6):426-428.
    This paper reports the results of a workshop held in January 2013 to begin the process of establishing standards for e-learning programmes in the ethics of research involving human participants that could serve as the basis of their evaluation by individuals and groups who want to use, recommend or accredit such programmes. The standards that were drafted at the workshop cover the following topics: designer/provider qualifications, learning goals, learning objectives, content, methods, assessment of participants and assessment of the course. The (...)
    Direct download (8 more)  
     
    Export citation  
     
    Bookmark   2 citations  
  7.  18
    Knowledge and Attitudes to Personal Genomics Testing for Complex Diseases Among Nigerians.Lawrence Fagbemiro & Clement Adebamowo - 2014 - BMC Medical Ethics 15 (1):34.
    The study examined the knowledge and attitudes to personal genomics testing for complex diseases among Nigerians and identified how the knowledge and attitudes vary with gender, age, religion, education and related factors.
    Direct download (6 more)  
     
    Export citation  
     
    Bookmark   1 citation  
  8.  5
    Qualitative Study of Comprehension of Heritability in Genomics Studies Among the Yoruba in Nigeria.Rasheed O. Taiwo, John Ipadeola, Temilola Yusuf, Faith Fagbohunlu, Gbemisola Jenfa, Sally N. Adebamowo & Clement A. Adebamowo - 2020 - BMC Medical Ethics 21 (1):1-8.
    Background With growth of genomics research in Africa, concern has arisen about comprehension and adequacy of informed consent given the highly technical terms used in this field. We therefore decided to study whether there are linguistic and cultural concepts used to communicate heritability of characters, traits and diseases in an indigenous African population. Methods We conducted Focus Group Discussions among 115 participants stratified by sex, age and socio-economic status and Key Informant Interviews among 25 stakeholders and Key Opinion Leaders among (...)
    Direct download (3 more)  
     
    Export citation  
     
    Bookmark