Complementary and alternative medicine practitioner consultations among those who have or have had cancer in a Norwegian total population (Nord-Trondelag Health Study): prevalence, socio-demographics and health perceptions

- Steinsbekk, A., Adams, J., Sibbritt, D., Johnsen, R.

Multidisciplinary care in cancer: do the current research outputs help?

- Carey, M., Sanson-Fisher, R., Lotfi-Jam, K., Schofield, P., Aranda, S.

Quality of life research: is there a difference in output between the major cancer types?

- Sanson-Fisher, R., Bailey, L. J., Aranda, S., D'Este, C., Stojanovski, E., Sharkey, K., Schofield, P.

Quality of life research: types of publication output over time for cancer patients, a systematic review

- Bailey, L. J., Sanson-Fisher, R., Aranda, S., D'Este, C., Sharkey, K., Schofield, P.

Cutting the research pie: a value-weighting approach to explore perceptions about psychosocial research priorities for adults with haematological cancers

- Paul, C. L., Sanson-Fisher, R., Douglas, H. E., Clinton-McHarg, T., Williamson, A., Barker, D.

Patient or treatment centre?: Where are efforts invested to improve cancer patients' psychosocial outcomes?

- Carey, M. L., Clinton-McHarg, T., Sanson-Fisher, R. W., Campbell, S., Douglas, H. E.

Cancer patients' concerns regarding access to cancer care: perceived impact of waiting times along the diagnosis and treatment journey

- Paul, C., Carey, M., Anderson, A., Mackenzie, L., Sanson-Fisher, R., Courtney, R., Clinton-McHarg, T.

Do cancer patients' psychosocial outcomes and perceptions of quality of care vary across radiation oncology treatment centres?

- Carey, M., Paul, C., Mackenzie, L., Sanson-Fisher, R., Cameron, E.

Financial and social impact of supporting a haematological cancer survivor

- Carey, M., Paul, C., Cameron, E., Lynagh, M., Hall, A., Tzelepis, F.

Psychological distress and unmet supportive care needs in cancer patients and carers who contact cancer helplines

- Chambers, S. K., Girgis, A., Occhipinti, S., Hutchison, S., Turner, J., Morris, B., Dunn, J.

Lymphoedema following treatment for head and neck cancer: impact on patients, and beliefs of health professionals

- McGarvey, A. C., Osmotherly, P. G., Hoffman, G. R., Chiarelli, P. E.

Measuring the unmet supportive care needs of cancer support persons: the development of the support person's unmet needs survey - short form

- Campbell, S. H., Carey, M., Sanson-Fisher, R., Barker, D., Turner, D., Taylor-Brown, J., Hall, A.

Cancer-related trauma, stigma and growth: the 'lived' experience of head and neck cancer

- Threader, J., Mccormack, L.

Health professional's perspectives of the barriers and enablers to cancer care for Indigenous Australians

- Meiklejohn, J. A., Adams, J., Valery, P. C., Walpole, E. T., Martin, J. H., Williams, H. M., Garvey, G.

Heads Up: a pilot trial of a psychological intervention to improve nutrition in head and neck cancer patients undergoing radiotherapy

- Britton, B., Baker, A., Clover, K., McElduff, P., Wratten, C., Carter, G.

Reduced prevalence of pain and distress during 4 years of screening with QUICATOUCH in Australian oncology patients

- Clover, K. A., Rogers, K. M., Britton, B., Oldmeadow, C., Attia, J., Carter, G. L.

The first step in ensuring patient-centred quality of care: ask the patient

- Zucca, A., Sanson-Fisher, R., Waller, A., Carey, M., Boadle, D.

Total depression and subtypes in prostate cancer survivors 10 years after treatment

- Sharpley, C. F., Bitsika, V., Christie, D. R. H., Bradford, R., Steigler, A., Denham, J. W.

A rapid review of needs assessment tools for post-treatment cancer survivors

- Jiao, M., Hall, A. E., Nolte, L., Piper, A., Lisy, K., Jefford, M.

Health care experiences among women diagnosed with gestational breast cancer

- Hammarberg, K, Sullivan, E, Javid, N, Duncombe, G, Halliday, L, Boyle, F, Saunders, C, Ives, A, Dickinson, J. E., Fisher, J