Evidence map›Paper›PMID 20629767›Full record

ArticleHealth expectations : an international journal of public participation in health care and health policy2010

Critical appraisal guidelines for assessing the quality and impact of user involvement in research.

David Wright, Claire Foster, Ziv Amir, Jim Elliott, Roger Wilson

Registry-linked trialAbstract read
In one paragraph

Article in Health expectations : an international journal of public participation in health care and health policy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03432143 (Community Members as Reviewers of Medical Journal Manuscripts), which is not on this map. Cited by 44 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 7 pooled it
–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.

NCT03432143 nacompletednot on this mapstarted 2018, after this paper: background citation

Community Members as Reviewers of Medical Journal Manuscripts

TypeinterventionalSponsorMetroHealth Medical CenterRan2018 to 2021Enrolled568ConditionsPeer Review, ResearchArmsCommunity Reviewers
3 · Its place in the literature

Who cites it

44 citing papers in PubMed, 7 syntheses or guidelines pooled it.

  1. Participatory research with carers: A systematic review and narrative synthesis.Health expectations : an international journal of public participation in health care and health policy · 2024
    Pooled it
  2. Pooled it
  3. Frameworks for supporting patient and public involvement in research: Systematic review and co-design pilot.Health expectations : an international journal of public participation in health care and health policy · 2019
    Pooled it
  4. Current trends in patient and public involvement in cancer research: A systematic review.Health expectations : an international journal of public participation in health care and health policy · 2019
    Pooled it
  5. Black and minority ethnic group involvement in health and social care research: A systematic review.Health expectations : an international journal of public participation in health care and health policy · 2018
    Pooled it
  6. Extent, quality and impact of patient and public involvement in antimicrobial drug development research: A systematic review.Health expectations : an international journal of public participation in health care and health policy · 2018
    Pooled it
  7. Patient and service user engagement in research: a systematic review and synthesized framework.Health expectations : an international journal of public participation in health care and health policy · 2015
    Pooled it
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  16. The Youth Patient and Public Involvement Café-A youth-led model for meaningful involvement with children and young people.Health expectations : an international journal of public participation in health care and health policy · 2022
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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

5 authors.

David WrightMacmillan Cancer Support, London, UK.
Claire Foster
Ziv Amir
Jim Elliott
Roger Wilson

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe involvement of service users in the design and conduct of health research has developed significantly in the UK in recent years. Involving service users is now seen as a core component of good research practice for all forms of health research. Given the important role that users have in health research, it is necessary to develop guidelines for their effective involvement. Whilst guidelines are currently being formulated, there remain no criteria with which to assess user involvement in published studies and funding applications.

objectiveThis study offers guidelines for appraising the quality and impact of user involvement in published papers and grant applications.

methodsAppraisal guidelines for user involvement have been developed on the basis of available literature and experiences from studies involving cancer patients and carers in the design and conduct of research.

findingsNine appraisal criteria have been developed. Criteria include issues such as 'Is the rationale for involving users clearly demonstrated?', 'Is the level of user involvement appropriate?', 'Is the recruitment strategy appropriate?', and 'Is the nature of training appropriate?'

conclusionGenerating and applying guidelines is vital if the impact of user involvement agenda in health research is to be understood.

Indexed as

Biomedical ResearchCommunity ParticipationGuidelines as TopicQuality ControlHumansNeoplasmsResearch DesignReview Literature as TopicUnited Kingdom

Identifiers

PMID20629767
PMCPMC5060547

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.