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  1.  8
    When Low Leisure-Time Physical Activity Meets Unsatisfied Psychological Needs: Insights From a Stress-Buffer Perspective.Markus Gerber, Sandrine Isoard-Gautheur, René Schilling, Sebastian Ludyga, Serge Brand & Flora Colledge - 2018 - Frontiers in Psychology 9.
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  2.  6
    Consent Requirements for Research with Human Tissue: Swiss Ethics Committee Members Disagree.Flora Colledge, Sophie De Massougnes & Bernice Elger - 2018 - BMC Medical Ethics 19 (1):93.
    In Switzerland, research with identifiable human tissue samples, and/or its accompanying data, must be approved by a research ethics committee before it can be allowed to take place. However, as the demand for such tissue has rapidly increased in recent years, and biobanks have been created to meet these needs, committees have had to deal with a growing number of such demands. Detailed instructions for evaluating every kind of tissue request are scarce. Committees charged with evaluating research protocols therefore sometimes (...)
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  3.  26
    Getting a Fair Share: Attitudes and Perceptions of Biobank Stakeholders Concerning the Fairness of Sample Sharing.Flora Colledge & Bernice Elger - 2015 - Bioethics 29 (6):424-430.
    Biobanks are essential tools for furthering a broad range of medical research areas. However, despite the plethora of national and international laws and guidelines which apply to them, the access and sharing policies of biobanks are only sparsely addressed by regulatory bodies. The ‘give and take’ process of biosample sharing is largely left up to biobank stakeholders themselves to oversee; it is therefore both in stakeholders' power, and in their interest, to ensure that sample accessibility is fair. This is an (...)
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  4.  10
    Sample and Data Sharing Barriers in Biobanking: Consent, Committees, and Compromises.Flora Colledge, Kirsten Persson, Bernice Elger & David Shaw - 2014 - Annals of Diagnostic Pathology 18 (2):78-81.
    The ability to exchange samples and data is crucial for the rapidly growth of biobanking. However, sharing is based on the assumption that the donor has given consent to a given use of her or his sample. Biobanking stakeholders, therefore, must choose 1 of 3 options: obtain general consent enabling multiple future uses before taking a sample from the donor, try to obtain consent again before sharing a previously obtained sample, or look for a legally endorsed way to share a (...)
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  5. What is a Biobank? Differing Definitions Among Biobank Stakeholders.David Shaw, Bernice Elger & Flora Colledge - 2014 - Clinical Genetics 85 (3):223-7.
    Aim: While there is widespread agreement on the broad aspects of what constitutes a biobank, there is much disagreement regarding the precise definition. This research aimed to describe and analyse the definitions of the term biobank offered by various stakeholders in biobanking. Methods: Interviews were conducted with 36 biobanking stakeholders with international experience currently working in Switzerland. Results: The results show that, in addition to the core concepts of biological samples and linked data, the planned use of samples (including sharing) (...)
     
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  6. “Conferring Authorship”: Biobank Stakeholders’ Experiences with Publication Credit in Collaborative Research.Flora Colledge, Bernice Elger & David Shaw - 2013 - PLoS ONE 8:e76686.
    Background: Multi-collaborator research is increasingly becoming the norm in the field of biomedicine. With this trend comes the imperative to award recognition to all those who contribute to a study; however, there is a gap in the current “gold standard” in authorship guidelines with regards to the efforts of those who provide high quality biosamples and data, yet do not play a role in the intellectual development of the final publication. -/- Methods and findings: We carried out interviews with 36 (...)
     
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  7.  6
    Correction To: Consent Requirements for Research with Human Tissue: Swiss Ethics Committee Members Disagree.Flora Colledge, Sophie De Massougnes & Bernice Elger - 2019 - BMC Medical Ethics 20 (1):24.
    It has come to our attention that in the original article [1] information regarding dates was omitted. The data in this study were obtained in Switzerland four years before the entering into force of the new Swiss Human Research Act in 2014, when the guidelines of the Swiss Academy of Medical Sciences ceased to apply. It is important for readers to know that at the time of the study there was no binding law in Switzerland, only the more open SAMS (...)
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  8.  7
    Acute Bouts of Exercising Improved Mood, Rumination and Social Interaction in Inpatients With Mental Disorders.Serge Brand, Flora Colledge, Sebastian Ludyga, Raphael Emmenegger, Nadeem Kalak, Dena Sadeghi Bahmani, Edith Holsboer-Trachsler, Uwe Pühse & Markus Gerber - 2018 - Frontiers in Psychology 9.
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  9.  6
    Obstacles to Widening Biosample Research.Flora Colledge, Jakob Passweg & Bernice Elger - 2019 - Science and Engineering Ethics 25 (1):113-128.
    Switzerland has an excellent culture of medical research and is a melting pot for medical experts with international expertise. Nevertheless, as in other countries, the resources available to medical researchers are not being fully used. Biological samples, which enable a host of medical research studies to be carried out without invasive methods involving patients, are frequently left unused or forgotten. The aim of this study is to examine the experiences of biobank stakeholders regarding the use or underuse of biosamples, in (...)
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