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The role of the internet, and in particular e-health, in chronic illness is a burgeoning phenomenon but its use to date in cancer care is somewhat limited. In this study an iterative consultative process was undertaken with the aim to develop a cancer care website that was patient-led, facilitated cancer self-management and had the potential to improve communication between patients, family and friends and health care professionals. The process involved multiple demonstrations of an already established base platform (SeeCare©) to potential end users (patients, family members and friends and health professionals) to identify required functions of a cancer care specific platform. An exhaustive list of specifications was prioritised and operationalised resulting in a web platform for people affected by cancer that was ready for testing in the clinical setting: CanCare.

Health ICT is rapidly gaining popularity among policy makers and health consumers. Specific platforms for use in cancer care are missing.
The aim of this pilot study was to: 1) test the feasibility, functionality and usability of a patient-led cancer care web platform: CanCare, in a sample of people undergoing cancer treatment and 2) ascertain if CanCare could enhance communication between patients, family, friends and health professionals.
Cancer patients receiving chemotherapy were invited to participate. Data were collected via semi-structured interviews, online surveys and a website usage program.
Nine patients with four different types of cancer completed the study. All saw the potential of the website but many found it too complex to use, particularly when unwell post treatment. Many were frustrated by the lack of integration with existing hospital systems and the need to enter relevant data manually. The cancer-specific information tab rated highly and was used extensively. The website used alone did not promote interactions between family and/or health professionals.
A patient-led cancer care website has the potential to help patients manage their cancer care but needs to be intuitive to use, integrated into hospital systems and requires significant family/carer and health professional engagement.

The rapid increase in gene-disease discoveries offers real promise of clinical applications for people and families affected by genetic conditions but for which health professionals are not prepared because of lack of training. The availability of clinically relevant education resources is critical to enabling nurses to develop the appropriate genetics-genomics knowledge and skills to provide optimum care for individuals and families.
The Internet is a core resource to support teaching and learning in nurse education. Evaluating such resources is important to maximise the education experience, particularly for subjects traditionally perceived by nurses as being difficult.

The use of mobile devices for professional, business, educational, personal and social purposes has accelerated exponentially over the last decade. Staff working in healthcare organisations, and patients and visitors using healthcare settings, understandably want to use mobile technology. Concerns have been raised about safety in terms of interference with equipment, and threats to privacy and dignity, yet less policy attention has been paid to infection risks.
Healthcare professional students were supplied with smartphones as part of a larger educational project. Devices collected from a sub-sample of students working in operating theatre contexts were sampled to estimate the cross-contamination potential of the technology. A longitudinal multiple measures design was used. Under laboratory conditions, samples were taken from surfaces using swabbing techniques followed by contact plating. The devices were subsequently cleaned with 70% isopropyl alcohol and returned to the students.
All devices demonstrated microbial contamination and over three quarters (86%) polymicrobial contamination. The technique and sites used to sample for microbial contamination influenced the levels of contamination identified. Swabbing alone was less likely to isolate polymicrobial contamination than contact plating, and some microorganisms were isolated only by contact plates and not by swabbing of the same area.
The findings from this study demonstrate further research is urgently needed to inform evidence-based infection control policy on the use of personal equipment such as mobile devices in the healthcare settings where contamination may have adverse effects on patients, staff and visitors.

This theoretically focused and discursive paper explores the role that participatory media can play in the field of nursing research and subsequent knowledge dissemination. Being able to gather information, sieve through it, access the latest developments in the field, and produce new information is a core part of the academic researcher’s role. Moreover, it could even be argued that for centuries it has been knowledge workers’ main tangible work currency. Indeed, the information age is not exclusive of the networked society. Haigh (2010) has noted that the information gathering and sharing opportunities, referred to as participatory media, offered by the second generation of web design that allow for information sharing – known as web 2.0 – have expanded our horizons beyond academia to the whole of the global research and education community. If we accept the premise that the use of social networks in the development of ideas is one that has a long and distinguished pedigree, then it can be seen that the role of participatory media is the latest iteration in its evolution. What makes this development such a challenge for nursing research in particular is that whilst nursing academia generally remains suspicious of the advantages offered by technology, this paper argues that the next 10–15 years will see an increase in the chasm between the existing research community and the next generation of researchers. This has been attributed to the difference between the two groups in their approach and attitude to technology.
