Research priority setting as a tool for justice and fairness in climate and health knowledge ecosystem
BackgroundResearch priority setting (RPS) exercises are a collective activity, used to determine which research topics or questions should be prioritised. This process helps allocate resources effectively and ensures that research efforts address the most pressing and relevant issues. However currently RPS exercises are conceptualised as a tool to reach consensus on what research should be prioritised, but in a justice blind manner. AimWe aim to bring a paradigm shift in how RPS is conceptualised and conducted by developing a conceptual framework to use RPS as a tool to enable justice and fairness in the climate and health knowledge ecosystemResearch MethodologyWe will use a multitude of methods, in an iterative manner to allow for effective integration of methods from different knowledge systems. The methods we will use are in-depth interviews, yarning (an Indigenous methodology), nominal group technique meetings, and a systematic review of existing RPS on climate change and health with a justice and eq
Submission to the Australian Government consultation on Australia’s draft ninth periodic report under Article 18 of the Convention on the Elimination of All Forms of Discrimination against Women (CEDAW)
Policy & Practice Report
Review of the Food Standards Australia New Zealand Act 1991 (the Act) submission on the impact analysis
Policy & Practice Report
COHESION-I: Implementation of the COmmunity HEalth System InnovatiON project in low- and middle-income countries
BackgroundCOHESION-I, a unique collaborative research initiative, is being implemented across Peru, Mozambique, Nepal, and India. Its primary focus is on understanding and enhancing the responsiveness of health systems. In India, the project takes a distinct approach, targeting the rural communities in the states of Telangana and Chhattisgarh. It will engage local communities in co-designing and implementing strategies to improve access to and utilisation of primary health care services provided by the public health system.The COHESION-I project aims to comprehensively understand primary healthcare responses for tracer conditions such as hypertension and diabetes mellitus for non-communicable diseases (NCDs) and lymphatic filariasis for neglected tropical diseases (NTDs). This research is crucial as it addresses pressing health challenges in low-resource settings, emphasising community engagement and participatory approaches. By focusing on national priorities such as improving primary health care and address
Feasibility study on options to limit unhealthy food marketing to children
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Submission to inquiry into Australia’s response to the priorities of Pacific Island countries and the Pacific region
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Food and Water for Life: working with indigenous communities to improve food and water security
BackgroundFood and water insecurity are critical factors contributing to poor nutrition and impacting planetary health. When communities lack access to an adequate and diverse food supply or clean water, they often resort to consuming nutritionally deficient options, leading to malnutrition and its associated health issues.By tackling these interconnected challenges, we can improve nutrition outcomes and safeguard the health of both people and the planet.AimThe overall goal of this five-year program is to mobilise communities and support them to transform local food systems.With a focus on remote communities in Australia, the Pacific Islands and India, this program will support communities to measure the impact of community-led initiatives to strengthen food and water security.Research Methodology:The program will the Household Food Insecurity Access Index Scale (HFIAS) and the Household Water Security Index Scale (HWISE) which are internationally recognised tools, to measure food and water security in commun
Submission to the House of Lords Committee on Food, Diet and Obesity Call for Evidence on Food, Diet and Obesity
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Submission to the Horizon Scan to Support Strategic Planning for the Australia New Zealand Food Regulatory System for 2023-2026
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Evaluating digoxin treatment in patients with rheumatic heart disease - A randomised placebo-controlled trial
Background
Digoxin is widely used in the medical management of patients with rheumatic heart disease (RHD), atrial fibrillation (AF), and for the treatment of heart failure (HF). Observational data from older patients with non-valvular AF suggest a higher mortality risk among those who received digoxin. However, patients with RHD are younger, without associated comorbidity, and it is unclear if digoxin will have similar adverse effects in these patients.
Extrapolating the results of studies in patients without valve disease, to patients with RHD may result in the underuse of an inexpensive treatment which has proven benefit in reducing hospitalisation for worsening HF. Therefore, there is a clear need for an adequately powered randomized controlled trial to answer: How does digoxin use affect mortality in patients with RHD? Does digoxin use reduce the incidence of worsening heart failure in patients with RHD?
Aim
To determine whether the use of digoxin in symptomatic patients with RHD af
New Zealanders’ support for alcohol control policies
Policy & Practice Report
Consent Study: Exploring the experiences of the consent process for Aboriginal and Torres Strait Islander people having cardiac surgery and participating in medical research
Background Gaining informed consent is a critical step before any medical procedures, or before taking part in medical research that requires effective communication. Cultural differences in concepts of health and healing, miscommunication, language barriers, and racism, hinder an appropriate informed consent process for Aboriginal and Torres Strait Islander peoples. Inappropriate informed consent processes worsen historical distrust and poor communication with health professionals widening health disparities for Aboriginal and Torres Strait Islander peoples.
Aims To explore Aboriginal and Torres Strait Islander people’s experience of informed consent process in relation to cardiac surgery and participation in medical research To explore clinician’s and researchers’ experience obtaining informed consent from Aboriginal and Torres Strait Islander people. Results will inform the development of strategies to ensure informed consent processes are culturally safe and assist Aborigina