scholarly journals Beyond categorisation: refining the relationship between subjects and objects in health research regulation

Author(s):  
Catriona McMillan ◽  
Edward Dove ◽  
Graeme Laurie ◽  
Emily Postan ◽  
Nayha Sethi ◽  
...  
2020 ◽  
Author(s):  
Catriona McMillan ◽  
Edward Dove ◽  
Graeme Laurie ◽  
Emily Postan ◽  
Nayha Sethi ◽  
...  

2011 ◽  
Vol 16 (10) ◽  
pp. 4239-4255 ◽  
Author(s):  
Madeleine Kangsen Scammell

Qualitative research uses nonnumeric data to understand people's opinions, motives, understanding, and beliefs about events or phenomena. In this analysis, I report the use of qualitative methods and data in the study of the relationship between environmental exposures and human health. A primary search for peer-reviewed journal articles dated from 1991 through 2008 included the following three terms: qualitative, environ*, and health. Searches resulted in 3,155 records. Data were extracted and findings of articles analyzed to determine where and by whom qualitative environmental health research is conducted and published, the types of methods and analyses used in qualitative studies of environmental health, and the types of information qualitative data contribute to environmental health. The results highlight a diversity of disciplines and techniques among researchers who used qualitative methods to study environmental health. Nearly all of the studies identified increased scientific understanding of lay perceptions of environmental health exposures. This analysis demonstrates the potential of qualitative data to improve understanding of complex exposure pathways, including the influence of social factors on environmental health, and health outcomes.


1972 ◽  
Vol 31 (2) ◽  
pp. 127-136 ◽  
Author(s):  
Ralph Patrick ◽  
H. Tyroler

Recent research in epidemiology has focused upon the relationship between rapid culture change and the health status of the participants. Many studies disclose that these transitional individuals suffer deleterious effects which can be attributed to the stresses generated by modification of their environment. Inquiry into the health consequences of culture change requires an instrument which will permit us to discern the level of modernization achieved by a particular community within a transitional social system. The present study describes the development and testing of such an instrument among the Papago Indians of southern Arizona, a tribe representing the entire spectrum of modernization phenomena from subsistence villages to urban enclaves. With the assistance of eight judges, 51 Papago Indian communities were scaled according to degree of modernization. The ratings obtained were subjected to several reliability tests and validated against conventional criteria of modernization: occupational structure, educational level, and kinship association. The modernization ratings were shown to be associated with the size of the community, but could be reproduced independently of this aspect of developmental change.


2019 ◽  
Vol 28 (2) ◽  
pp. 99-120 ◽  
Author(s):  
Isabel Fletcher ◽  
Stanislav Birko ◽  
Edward S. Dove ◽  
Graeme T. Laurie ◽  
Catriona McMillan ◽  
...  

1995 ◽  
Vol 23 (1) ◽  
pp. 15-29 ◽  
Author(s):  
Michael E. Mccullough

The theoretical and empirical literature on the relationship between prayer and health is critically reviewed. Although empirical research partially confirms that prayer promotes a variety of health outcomes, the empirical literature is characterized by weak methodologies that may contribute to the inconsistency of some findings. Recommendations are made for improving the quality of prayer and health research. An agenda for further empirical investigation of the relationship between prayer and health is proposed.


2021 ◽  
pp. medethics-2020-106941
Author(s):  
Mackenzie Graham ◽  
Nina Hallowell ◽  
Berge Solberg ◽  
Ari Haukkala ◽  
Joanne Holliday ◽  
...  

A rapidly growing proportion of health research uses ‘secondary data’: data used for purposes other than those for which it was originally collected. Do researchers using secondary data have an obligation to disclose individual research findings to participants? While the importance of this question has been duly recognised in the context of primary research (ie, where data are collected from participants directly), it remains largely unexamined in the context of research using secondary data. In this paper, we critically examine the arguments for a moral obligation to disclose individual research findings in the context of primary research, to determine if they can be applied to secondary research. We conclude that they cannot. We then propose that the nature of the relationship between researchers and participants is what gives rise to particular moral obligations, including the obligation to disclose individual results. We argue that the relationship between researchers and participants in secondary research does not generate an obligation to disclose. However, we also argue that the biobanks or data archives which collect and provide access to secondary data may have such an obligation, depending on the nature of the relationship they establish with participants.


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