Evidence map›Paper›PMID 23286245›Full record

ArticleTrials2013

Researchers' perceptions of ethical challenges in cluster randomized trials: a qualitative analysis.

Andrew D McRae, Carol Bennett, Judith Belle Brown, Charles Weijer, Robert Boruch, Jamie Brehaut, Shazia Chaudhry, Allan Donner, Martin Eccles, Jeremy Grimshaw and 2 more

Abstract read
In one paragraph

Article in Trials, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Trial
  2. Article
  3. Financial impact of the hospital pharmacy's participation in clinical trials.European journal of hospital pharmacy : science and practice · 2021
    Observational
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Andrew D McRaeDivision of Emergency Medicine, University of Calgary, Foothills Medical Centre, Rm C231, 1403 - 29 Street NW, Calgary, Alberta T2N 2T9, Canada. andrew.mcrae@albertahealthservices.ca
Carol Bennett
Judith Belle Brown
Charles Weijer
Robert Boruch
Jamie Brehaut
Shazia Chaudhry
Allan Donner
Martin Eccles
Jeremy Grimshaw
Merrick Zwarenstein
Monica Taljaard

Funding

Canadian Institutes of Health Research MOP85066Canadian Institutes of Health Research MOP89790
6 · The paper itself

Abstract

backgroundCluster randomized trials (CRTs) pose ethical challenges for investigators and ethics committees. This study describes the views and experiences of CRT researchers with respect to: (1) ethical challenges in CRTs; (2) the ethics review process for CRTs; and (3) the need for comprehensive ethics guidelines for CRTs.

methodsDescriptive qualitative analysis of interviews conducted with a purposive sample of 20 experienced CRT researchers.

resultsInformants expressed concern over the potential for bias that may result from requirements to obtain informed consent from research participants in CRTs. Informants suggested that the need for informed consent ought to be related to the type of intervention under study in a CRT. Informants rarely expressed concern regarding risks to research participants in CRTs, other than risks to privacy. Important issues identified in the research ethics literature, including fair subject selection and other justice issues, were not mentioned by informants. The ethics review process has had positive and negative impacts on CRT conduct. Informants stated that variability in ethics review between jurisdictions, and increasingly stringent ethics review in recent years, have hampered their ability to conduct CRTs. Many informants said that comprehensive ethics guidelines for CRTs would be helpful to researchers and research ethics committees.

conclusionsInformants identified key ethical challenges in the conduct of CRTs, specifically relating to identifying subjects, seeking informed consent, and the use of gatekeepers. These data have since been used to identify topics for in-depth ethical analysis and to guide the development of comprehensive ethics guidelines for CRTs.

Indexed as

PerceptionCluster AnalysisEthics Committees, ResearchEthics, ResearchHumansQualitative ResearchRandomized Controlled Trials as TopicResearch DesignResearcher-Subject RelationsResearch Personnel

Identifiers

PMID23286245
PMCPMC3561139

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.