TY - CHAP
T1 - Challenges and solutions for collecting data in health research
T2 - experiences of Australian doctoral and early career researchers
AU - Hamiduzzaman, Mohammad
AU - Taylor, Alan
AU - Lunnay, Belinda
AU - Kuot, Abraham
AU - Weckunanukul, Kannikar
AU - Smadi, Omar
AU - Pillen, Heath
AU - Shifaza, Fathimath
PY - 2021
Y1 - 2021
N2 - Inappropriate or poorly conducted data collection methods can reduce the validity or trustworthiness of research findings, which has implications for early career researchers trying to disseminate their work and for participants who have volunteered their time and personal information. In Australia, the National Health and Medical Research Council stipulates a governance process that covers standards of ethical practice and the legal responsibilities of researchers in respecting privacy and maintaining confidentiality and dignity of participants. However, data collection in clinical and community settings remains challenging for doctoral and early career researchers due to the complexities of research governance systems and issues with the involvement of participants in research activities. This chapter aims to report on the governance and fieldwork challenges encountered by the Australian doctoral and early career researchers during data collection. The content for this chapter comes from three doctoral and five early career researchers who each provided a summary of their data collection experiences and participated in virtual group discussions. A thematic analytical framework was used to synthesize and interpret the identified challenges and how researchers addressed them. The major challenges were related to the processes involved in research governance, expertise of researchers, health literacy of participants, fieldwork settings, approaching and designing questions, and research fatigue. In addressing the challenges, researchers drew upon personal qualities of persistence and resilience, a clear understanding of the study’s scope and duration, contextual knowledge about the research setting and study participants, piloting of data collection instruments, and relationships with participants. These findings have implications for how future doctoral researchers might anticipate and address challenges in the data collection, and for Australian supervisors in mentoring national and international doctoral researchers.
AB - Inappropriate or poorly conducted data collection methods can reduce the validity or trustworthiness of research findings, which has implications for early career researchers trying to disseminate their work and for participants who have volunteered their time and personal information. In Australia, the National Health and Medical Research Council stipulates a governance process that covers standards of ethical practice and the legal responsibilities of researchers in respecting privacy and maintaining confidentiality and dignity of participants. However, data collection in clinical and community settings remains challenging for doctoral and early career researchers due to the complexities of research governance systems and issues with the involvement of participants in research activities. This chapter aims to report on the governance and fieldwork challenges encountered by the Australian doctoral and early career researchers during data collection. The content for this chapter comes from three doctoral and five early career researchers who each provided a summary of their data collection experiences and participated in virtual group discussions. A thematic analytical framework was used to synthesize and interpret the identified challenges and how researchers addressed them. The major challenges were related to the processes involved in research governance, expertise of researchers, health literacy of participants, fieldwork settings, approaching and designing questions, and research fatigue. In addressing the challenges, researchers drew upon personal qualities of persistence and resilience, a clear understanding of the study’s scope and duration, contextual knowledge about the research setting and study participants, piloting of data collection instruments, and relationships with participants. These findings have implications for how future doctoral researchers might anticipate and address challenges in the data collection, and for Australian supervisors in mentoring national and international doctoral researchers.
KW - validity or trustworthiness of research findings
KW - National Health and Medical Research Council (NHMRC)
KW - standards of ethical practice
KW - legal responsibilities of researchers
KW - data collection in clinical and community settings
KW - doctoral and early career researchers
U2 - 10.4337/9781800376328.00008
DO - 10.4337/9781800376328.00008
M3 - Chapter
SN - 9781800376311
T3 - Elgar Field Guides
SP - 11
EP - 24
BT - Field Guide for Research in Community Settings
A2 - Islam, M.Rezaul
A2 - Khan, Niaz Ahmed
A2 - Ah, Siti Hajar Abu Bakar
A2 - Wahab, Haris Abd
A2 - Hamidi, Mashitah Binti
PB - Edward Elgar Publishing
CY - United Kingdom
ER -