Measuring Māori Health, Wellbeing, and Disability in Aotearoa Using a Web-Based Survey Methodology

• Published in: International journal of environmental research and public health Vol. 20; no. 18; p. 6797
• Main Authors: Ingham, Tristram R., Jones, Bernadette, Perry, Meredith, von Randow, Martin, Milne, Barry, King, Paula T., Nikora, Linda W., Sporle, Andrew
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 21.09.2023; MDPI
• Subjects: Biomedicine; Culture; Data collection; Disability; Health; Health disparities; Indigenous peoples; Inequality; Internet; Interviews; Maoris; Medical model; Native peoples; Polls & surveys; Qualitative research; Questionnaires; Racism; Research methodology; Weighting; Well being
• ISSN: 1660-4601; 1661-7827; 1660-4601
• DOI: 10.3390/ijerph20186797

High-quality evidence on the prevalence and impact of health, wellbeing, and disability among Māori, and other Indigenous peoples, is crucial for mitigating health inequities. Current surveys are predominantly centred within a biomedical paradigm, with the constructs mismatched with Indigenous worldviews. We aimed to develop and deploy an accessible and culturally grounded survey exploring Māori health, wellbeing, and disability using a Kaupapa Māori Research methodology. An extensive codesign process with Māori community partners interrogated all aspects of the design to ensure the process and outcomes met the needs of Māori. A large-scale, nationally representative survey of people of Māori descent was conducted. We used a multi-modal deployment approach that included online and alternate methods of completion. Our analysis included a novel dual-weighting system to ensure generalisability of results to the national Māori population. This achieved a survey of 7230 participants, a sample size comparable with government-administered surveys. The response rate was 11.1%, with 7.3% opting for alternate methods. A high completion rate of 93.4% was observed. This approach demonstrated a high level of engagement, resulting in an unprecedented collection of Māori health, wellbeing, and disability data. This highlights the importance of Indigenous codesign for ensuring accessible and culturally appropriate survey methods.