Published in Health Policy on June 15, 2007
Patients' and clinicians' research priorities. Health Expect (2010) 1.73
Operationalising a model framework for consumer and community participation in health and medical research. Aust New Zealand Health Policy (2007) 1.24
Policies to increase the social value of science and the scientist satisfaction. An exploratory survey among Harvard bioscientists. F1000Res (2014) 1.23
Status, challenges and facilitators of consumer involvement in Australian health and medical research. Health Res Policy Syst (2010) 0.98
From inclusion to independence--training consumers to review research. Health Res Policy Syst (2008) 0.86
Increasing the public health potential of basic research and the scientist satisfaction. An international survey of bioscientists. F1000Res (2016) 0.84
Consumer input into research: the Australian Cancer Trials website. Health Res Policy Syst (2011) 0.81
As the bell tolls: a foundation study on pancreatic cancer consumer's research priorities. BMC Res Notes (2009) 0.80
Supporting cancer survivors' participation in peer review: perspectives from NCI's CARRA program. J Cancer Surviv (2013) 0.75
Developing a quality criteria framework for patient decision aids: online international Delphi consensus process. BMJ (2006) 9.04
A systematic review on communicating with patients about evidence. J Eval Clin Pract (2006) 2.91
Interventions before consultations to help patients address their information needs by encouraging question asking: systematic review. BMJ (2008) 2.33
Anxiety and depression among long-term survivors of cancer in Australia: results of a population-based survey. Med J Aust (2009) 2.20
Clinical practice guidelines for communicating prognosis and end-of-life issues with adults in the advanced stages of a life-limiting illness, and their caregivers. Med J Aust (2007) 1.99
Incidence of metastatic breast cancer in an Australian population-based cohort of women with non-metastatic breast cancer at diagnosis. Med J Aust (2012) 1.95
Assessing health-related quality of life in gynecologic oncology: a systematic review of questionnaires and their ability to detect clinically important differences and change. Int J Gynecol Cancer (2010) 1.72
What do cancer support groups provide which other supportive relationships do not? The experience of peer support groups for people with cancer. Soc Sci Med (2005) 1.69
Patient entry into randomized controlled trials of colorectal cancer treatment: factors influencing participation. Surgery (2003) 1.63
Clinical trials of palliative chemotherapy in platinum-resistant or -refractory ovarian cancer: time to think differently? J Clin Oncol (2013) 1.63
A randomised controlled trial of proactive telephone counselling on cold-called smokers' cessation rates. Tob Control (2010) 1.62
Communicating risk information: the influence of graphical display format on quantitative information perception-Accuracy, comprehension and preferences. Patient Educ Couns (2007) 1.56
Brief assessment of adult cancer patients' perceived needs: development and validation of the 34-item Supportive Care Needs Survey (SCNS-SF34). J Eval Clin Pract (2009) 1.55
Australian general practitioners' and oncology specialists' perceptions of barriers and facilitators of access to specialist palliative care services. J Palliat Med (2011) 1.51
Breast cancer survivors' supportive care needs 2-10 years after diagnosis. Support Care Cancer (2006) 1.45
Survivorship care after breast cancer treatment--experiences and preferences of Australian women. Breast (2011) 1.43
Survivorship care after breast cancer. Aust Fam Physician (2008) 1.40
Prevalence and correlates of cancer survivors' supportive care needs 6 months after diagnosis: a population-based cross-sectional study. BMC Cancer (2012) 1.32
Supportive care needs: are patients with lung cancer a neglected population? Psychooncology (2006) 1.27
Guidelines for the diagnosis and treatment of malignant pleural mesothelioma. J Thorac Dis (2013) 1.27
Long-term survival from gynecologic cancer: psychosocial outcomes, supportive care needs and positive outcomes. Gynecol Oncol (2006) 1.27
Operationalising a model framework for consumer and community participation in health and medical research. Aust New Zealand Health Policy (2007) 1.24
Response rates in GP surveys - trialling two recruitment strategies. Aust Fam Physician (2011) 1.21
The relationship between available support, unmet needs and caregiver burden in patients with advanced cancer and their carers. Psychooncology (2005) 1.19
Increasing oncologists' skills in eliciting and responding to emotional cues: evaluation of a communication skills training program. Psychooncology (2008) 1.18
Young adult cancer survivors' psychosocial well-being: a cross-sectional study assessing quality of life, unmet needs, and health behaviors. Support Care Cancer (2011) 1.17
Do couple-based interventions make a difference for couples affected by cancer? A systematic review. BMC Cancer (2012) 1.16
Psychological treatment outcomes for cancer patients: what do meta-analyses tell us about distress reduction? Psychooncology (2011) 1.13
Parental adjustment to the completion of their child's cancer treatment. Pediatr Blood Cancer (2010) 1.11
Do personal stories make patient decision aids more effective? A critical review of theory and evidence. BMC Med Inform Decis Mak (2013) 1.11
The shortage of medical oncologists: the Australian Medical Oncologist Workforce Study. Med J Aust (2012) 1.10
Efficacy of tailored-print interventions to promote physical activity: a systematic review of randomised trials. Int J Behav Nutr Phys Act (2011) 1.09
Anywhere, anytime: retail access to tobacco in New South Wales and its potential impact on consumption and quitting. Soc Sci Med (2010) 1.09
Walking a mile in their shoes: anxiety and depression among partners and caregivers of cancer survivors at 6 and 12 months post-diagnosis. Support Care Cancer (2012) 1.08
Interpreting differences in patterns of supportive care needs between patients with breast cancer and patients with colorectal cancer. Psychooncology (2012) 1.07
Has the investment in public cancer education delivered observable changes in knowledge over the past 10 years? Cancer (2003) 1.05
Identifying patient information needs about cancer clinical trials using a Question Prompt List. Patient Educ Couns (2010) 1.05
The use and perceived benefits resulting from the use of complementary and alternative medicine by cancer patients in Australia. Asia Pac J Clin Oncol (2010) 1.05
What do patients want? Patient preferences and surrogate decision making in the treatment of colorectal cancer. Dis Colon Rectum (2003) 1.05
Supportive care needs in Hong Kong Chinese women confronting advanced breast cancer. Psychooncology (2012) 1.03
Is it worth the risk? A systematic review of instruments that measure risk propensity for use in the health setting. Soc Sci Med (2005) 1.03
A bridge between cultures: interpreters' perspectives of consultations with migrant oncology patients. Support Care Cancer (2010) 1.03
Information about tests for breast cancer: what are we telling people? J Fam Pract (2002) 1.03
Meeting the decision-making preferences of patients with breast cancer in oncology consultations: impact on decision-related outcomes. J Clin Oncol (2012) 1.02
Telephone recruitment into a randomized controlled trial of quitline support. Am J Prev Med (2009) 1.02
From inside the bubble: migrants' perceptions of communication with the cancer team. Support Care Cancer (2010) 1.01
"I can't do this, it's too much": building social inclusion in cancer diagnosis and treatment experiences of Aboriginal people, their carers and health workers. Int J Public Health (2013) 1.01
Sharing vs. caring--the relative impact of sharing decisions versus managing emotions on patient outcomes. Patient Educ Couns (2011) 1.01
Medical Qigong for cancer patients: pilot study of impact on quality of life, side effects of treatment and inflammation. Am J Chin Med (2008) 1.00
Flourishing or floundering? Prevalence and correlates of anxiety and depression among a population-based sample of adult cancer survivors 6months after diagnosis. J Affect Disord (2011) 1.00
Pushing up daisies: implicit and explicit language in oncologist-patient communication about death. Support Care Cancer (2006) 0.99
Can a single question effectively screen for burnout in Australian cancer care workers? BMC Health Serv Res (2010) 0.99
The unmet needs of partners and caregivers of adults diagnosed with cancer: a systematic review. BMJ Support Palliat Care (2012) 0.99
Increasing hospital-wide delivery of smoking cessation care for nicotine-dependent in-patients: a multi-strategic intervention trial. Addiction (2009) 0.98
Status, challenges and facilitators of consumer involvement in Australian health and medical research. Health Res Policy Syst (2010) 0.98
Facilitating needs based cancer care for people with a chronic disease: Evaluation of an intervention using a multi-centre interrupted time series design. BMC Palliat Care (2010) 0.98
All's well that ends well? Quality of life and physical symptom clusters in long-term cancer survivors across cancer types. J Pain Symptom Manage (2012) 0.98
Prescribing sunshine: a cross-sectional survey of 500 Australian general practitioners' practices and attitudes about vitamin D. Int J Cancer (2011) 0.97
Survivorship care after breast cancer: follow-up practices of Australian health professionals and attitudes to a survivorship care plan. Asia Pac J Clin Oncol (2010) 0.97
Validity, reliability and clinical feasibility of a Needs Assessment Tool for people with progressive cancer. Psychooncology (2010) 0.97
Symptom control in patients with recurrent ovarian cancer: measuring the benefit of palliative chemotherapy in women with platinum refractory/resistant ovarian cancer. Int J Gynecol Cancer (2009) 0.97
Rapid assessment of psychosocial well-being: are computers the way forward in a clinical setting? Qual Life Res (2002) 0.96
A critical review of the effects of medical Qigong on quality of life, immune function, and survival in cancer patients. Integr Cancer Ther (2011) 0.96
Nicotine replacement therapy products over the counter: real-life use in the Australian community. Aust N Z J Public Health (2003) 0.95
Distressed partners and caregivers do not recover easily: adjustment trajectories among partners and caregivers of cancer survivors. Ann Behav Med (2012) 0.95
RCT of a client-centred, caseworker-delivered smoking cessation intervention for a socially disadvantaged population. BMC Public Health (2011) 0.94
Conquer fear: protocol of a randomised controlled trial of a psychological intervention to reduce fear of cancer recurrence. BMC Cancer (2013) 0.94
Prevalence and determinants of Australian adolescents' and adults' weekend sun protection and sunburn, summer 2003-2004. J Am Acad Dermatol (2008) 0.94
Shared decision making in oncology: assessing oncologist behaviour in consultations in which adjuvant therapy is considered after primary surgical treatment. Health Expect (2010) 0.93
Health literacy in relation to cancer: addressing the silence about and absence of cancer discussion among Aboriginal people, communities and health services. Health Soc Care Community (2013) 0.93
Adding value to clinical trial registries: insights from Australian Cancer Trials Online, a website for consumers. Clin Trials (2011) 0.93
Measuring patient preference and surgeon choice. Surgery (2008) 0.92
Changes in quality of life in patients with advanced cancer: evidence of response shift and response restriction. J Psychosom Res (2005) 0.92
Evaluating the utility of a patient decision aid for potential participants of a prostate cancer trial (RAVES-TROG 08.03). Radiother Oncol (2011) 0.92
Family information needs at childhood cancer treatment completion. Pediatr Blood Cancer (2011) 0.92
The motherhood choice: a decision aid for women with multiple sclerosis. Patient Educ Couns (2007) 0.92
A Rasch analysis of the Hospital Anxiety and Depression Scale (HADS) among cancer survivors. Psychol Assess (2013) 0.91
A comparison of data quality and practicality of online versus postal questionnaires in a sample of testicular cancer survivors. Psychooncology (2011) 0.91
Patient-doctor communication: use of complementary and alternative medicine by adult patients with cancer. J Soc Integr Oncol (2010) 0.91
Increasing smoking cessation care provision in hospitals: a meta-analysis of intervention effect. Nicotine Tob Res (2009) 0.91
Enhancing decision making about participation in cancer clinical trials: development of a question prompt list. Support Care Cancer (2010) 0.90
Cancer knowledge and skills of interns in Australia and New Zealand in 2001: comparison with 1990, and between course types. Med J Aust (2003) 0.90
Inferior health-related quality of life and psychological well-being in immigrant cancer survivors: a population-based study. Eur J Cancer (2013) 0.90
Australian breast cancer specialists' involvement in multidisciplinary treatment planning meetings. Breast (2008) 0.90
Rasch analysis of the Hospital Anxiety and Depression Scale among caregivers of cancer survivors: implications for its use in psycho-oncology. Psychooncology (2010) 0.90
The Cancode interaction analysis system in the oncological setting: reliability and validity of video and audio tape coding. Patient Educ Couns (2005) 0.90
Patient and physician preferences for surgical and adjuvant treatment options for rectal cancer. Arch Surg (2008) 0.90
Implementing patient decision support tools: moving beyond academia? Patient Educ Couns (2009) 0.89
A randomized controlled trial of a standardized educational intervention for patients with cancer pain. J Pain Symptom Manage (2010) 0.89
Testing the utility of a cancer clinical trial specific Question Prompt List (QPL-CT) during oncology consultations. Patient Educ Couns (2012) 0.89
Prevalence and predictors of the short-term trajectory of anxiety and depression in the first year after a cancer diagnosis: a population-based longitudinal study. J Clin Oncol (2013) 0.88
Exercise and nutrition routine improving cancer health (ENRICH): the protocol for a randomized efficacy trial of a nutrition and physical activity program for adult cancer survivors and carers. BMC Public Health (2011) 0.88
Identifying and prioritising gaps in colorectal cancer trials research in Australia. Med J Aust (2012) 0.88
The Quality of Life Questionnaire Core 30 (QLQ-C30) and Functional Assessment of Cancer-General (FACT-G) differ in responsiveness, relative efficiency, and therefore required sample size. J Clin Epidemiol (2013) 0.88
Travelling all over the countryside: travel-related burden and financial difficulties reported by cancer patients in New South Wales and Victoria. Aust J Rural Health (2011) 0.87
Cost of treating chronic hepatitis B: comparison of current treatment guidelines. World J Gastroenterol (2012) 0.87