2020
DOI: 10.1177/2054358120964119
|View full text |Cite
|
Sign up to set email alerts
|

Ethical Issues in the Design and Conduct of Pragmatic Cluster Randomized Trials in Hemodialysis Care: An Interview Study With Key Stakeholders

Abstract: Background: Pragmatic cluster randomized trials (CRTs) offer an opportunity to improve health care by answering important questions about the comparative effectiveness of treatments using a trial design that can be embedded in routine care. There is a lack of empirical research that addresses ethical issues generated by pragmatic CRTs in hemodialysis. Objective: To identify stakeholder perceptions of ethical issues in pragmatic CRTs conducted in hemodialysis. Design: Qualitative study using semi-structured int… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

1
3
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
5
1

Relationship

0
6

Authors

Journals

citations
Cited by 6 publications
(4 citation statements)
references
References 48 publications
1
3
0
Order By: Relevance
“…After analysis of the interview data, we identified five ethically relevant themes from the respondents’ experiences and opinions about the ethical challenges posed by CRTs in public health facilities. Our findings are consistent with what has been reported in literature (Chaudhry et al, 2013; GFBR, 2017; Goldstein et al, 2018; McRae et al, 2013; Nicholls et al, 2020). However, these ethical challenges manifest themselves differently in the unique environment of health facilities in Malawi.…”
Section: Findings and Discussionsupporting
confidence: 94%
“…After analysis of the interview data, we identified five ethically relevant themes from the respondents’ experiences and opinions about the ethical challenges posed by CRTs in public health facilities. Our findings are consistent with what has been reported in literature (Chaudhry et al, 2013; GFBR, 2017; Goldstein et al, 2018; McRae et al, 2013; Nicholls et al, 2020). However, these ethical challenges manifest themselves differently in the unique environment of health facilities in Malawi.…”
Section: Findings and Discussionsupporting
confidence: 94%
“…However, they made suggestions for integrating intervention delivery with other routine care activities while in hospital to help minimize identified burdens of clinical trial participation, such as need for additional testing and/or return visits, financial challenges, and concerns about safety. 35,36 Embedding trial processes within clinical workflows, such as timing cilastatin administration with other medications or coordinating laboratory tests with routine inpatient bloodwork, could further reduce the burden for healthcare team members and help to promote trial feasibility. 37 Important concerns raised by participants about allocation to a placebo arm when the cilastatin intervention might help prevent poor AKI-associated outcomes align with patients' perspectives on rare disease trial design from a qualitative study by Gaasterland et al 38 As patients view a novel intervention as a source of hope, the possibility of not receiving a potentially beneficial intervention may compromise this hope, the perceived benefits of trial participation, and ultimately patients' willingness to enrol in trials of this design.…”
Section: Discussionmentioning
confidence: 99%
“…Open label studies and shared control groups could help patient recruitment, provided the stringent criteria of study design outlined in the present paper are applied. Propensity score matching 103 and cluster randomized trials 104 are alternative means of making it easier to conduct trials in FSGS.…”
Section: Targeting Inflammation and Fibrosismentioning
confidence: 99%