Developing registries of volunteers: key principles to manage issues regarding personal information protection

Much biomedical research cannot be performed without recruiting human subjects. Increasingly, volunteer registries are being developed to assist researchers with this challenging task. Yet, volunteer registries raise confidentiality issues. Having recently developed a registry of volunteers, the authors searched for normative guidance on how to implement the principle of confidentiality. The authors found that the protection of confidentiality in registries are based on the 10 key elements which are elaborated in detail in the Canadian Standards Association Model Code. This paper describes how these 10 detailed key principles can be used during the developmental stages of volunteer registries.

[1]  Jeffrey P. Krischer,et al.  An automated communication system in a contact registry for persons with rare diseases: scalable tools for identifying and recruiting clinical research participants. , 2009, Contemporary clinical trials.

[2]  R. Weintraub,et al.  Establishment of an Australian National Genetic Heart Disease Registry. , 2008, Heart, lung & circulation.

[3]  W. Katon,et al.  Implementing a clinical and research registry in obstetrics: overcoming the barriers. , 2007, General hospital psychiatry.

[4]  R. Sandler,et al.  Research recruitment through US central cancer registries: balancing privacy and scientific issues. , 2006, American journal of public health.

[5]  John Whyte,et al.  A patient registry for cognitive rehabilitation research: a strategy for balancing patients' privacy rights with researchers' need for access. , 2005, Archives of physical medicine and rehabilitation.

[6]  Protecting Medical Record Information: Start Your Research Registries Today , 2005, The Laryngoscope.

[7]  J. Schildkraut,et al.  Ethical ramifications of alternative means of recruiting research participants from cancer registries , 1999, Cancer.

[8]  Ahmad Husseini,et al.  Canadian standards association , 1993 .

[9]  Z. Bankowski,et al.  Council for International Organizations of Medical Sciences , 1991 .

[10]  Joan E Sieber,et al.  A census of subject pool characteristics and policies. , 1989, The American psychologist.

[11]  D. Istance Organization for Economic Co-operation and Development , 1966, Nature.