Exploring the early experiences of assisted dying in Aotearoa New Zealand : a qualitative study protocol

Article indépendant

YOUNG, Jessica | DEHKHODA, Aida | AHURIRI-DRISCOLL, Annabel | CHEUNG, Gary | DIESFELD, Kate | EGAN, Richard | KARAKA-CLARKE, Te Hurinui | MOEKE-MAXWELL, Tess | REID, Kate | ROBINSON, Jackie | SNELLING, Jeanne | WHITE, Ben | WINTERS, Janine

INTRODUCTION: Increasing numbers of jurisdictions are legalising assisted dying (AD). Developing research protocols to study the experiences and outcomes of legislation is imperative. AD is a topic that, by nature of its complexity and inherent ethical issues, lends itself to qualitative research. Using the objectives of the statutory framework, this qualitative study aims to provide a robust review of the newly formed AD service in New Zealand and the extent to which it is safe, people-centred, dignity-enhancing, accessible and available equitably to all eligible people. METHODS AND ANALYSIS: The research uses an appreciative inquiry design to focus on what is working well, what could be improved, what constitutes the ‘ideal’ and how to enable people to achieve that ideal. We are using online semi-structured interviews and face-to-face focus groups to explore the experiences of key stakeholders: eligible/ineligible service users; eligible/ineligible service users with impairments; families of service users; AD providers; non-providers (providers who object to AD and others who are not directly involved in providing AD but are not opposed in principle); health service leaders; and Maori community members. An estimated 110 participants will be interviewed. We will conduct thematic and regulatory analyses of data. ETHICS AND DISSEMINATION: The ethical aspects of this study have been approved by the Northern A Health and Disability Ethics Committee through the full review pathway (2023 EXP 18493). To disseminate the findings, we will draft resources to support interviewee groups, to be developed with feedback from stakeholder meetings. We will submit evidence-based recommendations to inform the government review of the End of Life Choice Act 2019. Findings will be disseminated in peer-reviewed publications, conferences, webinars, media, stakeholder feedback sessions and accessible research briefings.

http://dx.doi.org/10.1136/bmjopen-2024-090118

Voir la revue «BMJ Open, 14»

Autres numéros de la revue «BMJ Open»

Consulter en ligne

Suggestions

Du même auteur

Exploring the early experiences of assisted d...

Article indépendant | YOUNG, Jessica | BMJ Open | n°10 | vol.14

INTRODUCTION: Increasing numbers of jurisdictions are legalising assisted dying (AD). Developing research protocols to study the experiences and outcomes of legislation is imperative. AD is a topic that, by nature of its complexit...

What do health care professionals want to kno...

Article | YOUNG, Jessica | BMC palliative care | n°1 | vol.22

BACKGROUND: New Zealand recently introduced law permitting terminally ill people to request and receive assisted dying (AD) in specified circumstances. Given the nature and complexity of this new health service, research is vital ...

What do health care professionals want to kno...

Article indépendant | YOUNG, Jessica | BMC palliative care | n°1 | vol.22

BACKGROUND: New Zealand recently introduced law permitting terminally ill people to request and receive assisted dying (AD) in specified circumstances. Given the nature and complexity of this new health service, research is vital ...

De la même série

Identifying specific subgroups of older patie...

Article indépendant | VISADE, Fabien | BMJ Open | n°1 | vol.15

OBJECTIVE: To identify specific subgroups of older patients at risk of repeated hospital readmissions and death. DESIGN: Prospective, multicentre, DAMAGE (Patient Outcomes After Hospitalization in Acute Geriatric Unit) cohort of a...

Top 10 palliative care research priorities in...

Article indépendant | BARBARET, Cécile | BMJ Open | n°1 | vol.15

INTRODUCTION: As one means to avoid waste in research investment, involving patients as full partners in research has become increasingly frequent. There is clearly a low level of investment in palliative care research. Following ...

Evaluation of electronic palliative care coor...

Article indépendant | ALIED, Marcel | BMJ Open | n°3 | vol.15

INTRODUCTION: Electronic Palliative Care Coordination Systems (EPaCCS) are electronic registers that aim to facilitate documentation and sharing of up-to-date information about patients' end-of-life preferences and plans for care ...

Support needs and preferences for people with...

Article indépendant | CUBIS, Lee | BMJ Open | n°4 | vol.15

INTRODUCTION: People with multiple sclerosis (MS) live with a progressive condition that can result in complex disability support needs. Consequently, they may require specialised care and assistive technology to maintain independ...

Understanding aims, successes and challenges ...

Article indépendant | CROOKS, Jodie | BMJ Open | n°1 | vol.14

BACKGROUND: Due to the recognition that people experiencing homelessness (PEH) often die young and unsupported, a growing number of initiatives focusing on palliative care and homelessness are emerging across the UK. However, ther...

Chargement des enrichissements...