Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.584907
Title: After genetics : Huntington's disease, local data, global neuroscience
Author: Hughes, Jacqueline
Awarding Body: Cardiff University
Current Institution: Cardiff University
Date of Award: 2010
Availability of Full Text:
Access through EThOS:
Access through Institution:
Abstract:
A 36 month ethnographic study of a research clinic with a combined role of disease management, included non participant observation of clinic routines, neurological consultations, motor and cognitive research testing of patients, plus interviews with patients, carers, clinicians, researchers and others associated with the clinic. A 'shift' of Huntington's disease into neurology was observed plus standardisation of research activities on an international scale. The clinic acts as a recruitment site for other experimental research. Research questions were - does a neurological instead of genetic framework make a difference to how the disease is regarded, and, what does research participation mean for patients and clinicians A neurological framework appeared to encourage research participation because patients and carers considered it an opportunity for experimental treatment, including stem cell transplantation to the brain. Three analytic themes revealed: 'blurring' in operation of research and care, performances by all clinic actors linked to social and research expectations, plus the neurology framework increased patients' hopes in research aims. Sub themes included biomedicalisation, research translation, emotional work, research limitations, social benefits and transplant hope. Clinic researchers noticed tension in their dual research/care role, patients and carers noticed they were given time but little practical care.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.584907  DOI: Not available
Share: