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Public Attitudes to Genomics: Vignette Studies, 2004
Abstract copyright UK Data Service and data collection copyright owner.These vignette studies form part of a wider project to provide a basic understanding of current attitudes among the public towards a range of new genetic technologies. Public attitudes and behaviour toward developments in this area of science are likely to be conditional, at least in part, upon...
Doing Embryo Ethics: Safety and Efficacy in Research and Practice, 2004-2007
Abstract copyright UK Data Service and data collection copyright owner.This qualitative project explored the social and discursive construction of ethics in research laboratories and clinics working with human embyros. The dataset contains semi-structured interviews with clinicians, scientists, and related professionals.
The study contributed towards understanding...
Human Embryonic Stem Cell Research in China and Japan, 2006-2007
Abstract copyright UK Data Service and data collection copyright owner.This is a qualitative data collection.
The bioethics of human embryonic stem cell research (HESR) is controversial, including in Asia. After the 2001 US-moratorium on the federal funding of HESR, some Asian countries jumped into the 'bioethical vacuum', claiming that Asian countries do not suffer from...
Social Dynamics of Public Engagement in Stem Cell Research, 2005-2007
Abstract copyright UK Data Service and data collection copyright owner.This is a qualitative data collection.
This project had two main aims: to investigate the range of views and concerns of people hold about stem cell research (SCR), and to explore critically the scope for increasing public engagement in SCR through a range of public engagement techniques. The research...
Medical Student Survey, University of Birmingham, 1974
Abstract copyright UK Data Service and data collection copyright owner.To collect a large amount of information about medical students, with particular emphasis upon details of their cultural activities and their political and ethical views. The intention was to discover any correlations between these activities. Data were collected about attitudes towards general practice...
Best practices in sharing individual level health research data in low and middle income settings: A qualitative study of views of stakeholders in India
Transcripts of in-depth interviews and group discussions with managers, researchers, ethics committee members, field data collectors and community members on the issues around ethical data sharing in the context of research involving women and children in urban India. We interviewed researchers, managers, and research participants associated with a Mumbai non-governmental...
State strategies of governance in global biomedical innovation: The impact of China and India 2012-2015
Interviews: Focusing on four case studies, the research interviews focus on:
1.Primary components and directions of China and India's innovation policies, strategies and actions.
2.How strategies align with or depart from those employed by the developed economies of the UK, EU, North America, and Japan.
3.The extent to which the Rising Powers strategies engage with,...
Interviews on Trials Transparency at Public Research Institutions in the UK, 2020-2021
Ensuring the reporting of clinical research is essential to informed evidence generation in medicine. The UK has seen politicians, funders, and other stakeholder focus on transparency which has translated to pressure on sponsors to ensure greater transparency of their research. This study aimed to collect the institutional perspective to transparency issues in clinical...
Non-invasive Prenatal Testing Study: Comparison England, France, Germany, 2021-2022
This project proposed a new approach to explore ethical issues arising from the clinical implementation of genomics in antenatal care in the twenty first century. Situated at the interface between sociology, bioethics and law/social policy this research seeks to gain in-depth understanding of the situations in which these questions emerge and are experienced by the...
Non-invasive Prenatal Testing Study: Comparison England, France, Germany, 2021-2022
This project proposed a new approach to explore ethical issues arising from the clinical implementation of genomics in antenatal care in the twenty first century. Situated at the interface between sociology, bioethics and law/social policy this research seeks to gain in-depth understanding of the situations in which these questions emerge and are experienced by the...
Secondary Use of Health and Social Care Data 2016
This survey charted Finnish citizens' as well as social and healthcare service professionals' attitudes and views concerning secondary use of health and social care data in research and development of services. The study contained two target groups: (1) persons who suffered or had a close relative or acquaintance who suffered from one or more chronic conditions, diseases or...
Biological and regenerative therapies in professional football and cycling in the UK
The data collection consists of: a list of technologies resulting from an online survey of 'bio' products available on the market and the companies marketing them (see Related resources); a collection of bibliographic references and abstracts of published scientific articles on biological therapy topics including Platelet Rich Plasma (PRP), stem cells, and others in trial or...
Military healthcare professionals experiences of ethical challenges whilst on Ebola humanitarian deployment
20 transcribed and anonymised interviews with military personnel returning from the military-run Ebola treatment centre , Kerry Town, Sierra Leone between March-July 2015. The sample included three broad groups: doctors (7), nurses and healthcare assistants (6), and others such as personal protective equipment monitors, lab technicians and mortuary attendants (7). Interviews...
Wellcome Trust Monitor Waves 1-3 Combined Adults Data, 2009-2015
Abstract copyright UK Data Service and data collection copyright owner.The Wellcome Trust Monitor is a unique survey of UK adults' (and in some waves, young people's) views around science and biomedical research. The findings are representative of the UK population and provide fresh and significant insights to inform science communication practice and how research priorities...