Evidence map›Paper›PMID 17524010›Full record

ArticleHealth expectations : an international journal of public participation in health care and health policy2007

User involvement in the development of a research bid: barriers, enablers and impacts.

Sophie Staniszewska, Nicola Jones, Mary Newburn, Shanit Marshall

Abstract read
In one paragraph

Article in Health expectations : an international journal of public participation in health care and health policy, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 6 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.

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

54 citing papers in PubMed, 6 syntheses or guidelines pooled it.

  1. Meaningful patient and public involvement in digital health innovation, implementation and evaluation: A systematic review.Health expectations : an international journal of public participation in health care and health policy · 2022
    Pooled it
  2. Pooled it
  3. 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
  4. Mapping the impact of patient and public involvement on health and social care research: a systematic review.Health expectations : an international journal of public participation in health care and health policy · 2014
    Pooled it
  5. Quality and acceptability of patient-reported outcome measures used in chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME): a systematic review.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2012
    Pooled it
  6. Getting ready for user involvement in a systematic review.Health expectations : an international journal of public participation in health care and health policy · 2009
    Pooled it
  7. Article
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  11. Developing a research community within an online healthcare feedback platform.Health expectations : an international journal of public participation in health care and health policy · 2023
    Article
  12. Article
  13. A qualitative evaluation of coproduction of research: 'If you do it properly, you will get turbulence'.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

4 authors.

Sophie StaniszewskaRCN Institute, Radcliffe Infirmary, Oxford, UK. sophie.staniszewska@rcn.org.uk
Nicola Jones
Mary Newburn
Shanit Marshall

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo involve users in the development of a research bid to examine parents' experiences of having a pre-term baby, and to examine the barriers, enablers and impacts of user involvement.

designA mainly collaborative approach to user involvement was adopted, although different types of involvement were evident at different stages of the project. Users' experiences and perspectives provided the focus for the regular meetings which underpinned the writing of the research bid. The researcher acted as a facilitator in the development of the bid, with input from users and the wider advisory group. MAIN OUTCOMES: User involvement had an important impact on the development of the research aims, methods and on ethical aspects. Through careful collaboration a research bid was produced which was rooted in users' experiences, whilst also addressing key research questions. Key enablers for involvement included good working relationships, funding for the lead researchers time. Barriers included lack of financial support for users, the time-consuming nature of involvement and the language of research.

conclusionsIf user involvement remains an international policy imperative with little if any support at the vital stage of bid development, policy-makers, service user organizations, researchers, health service providers and commissioners will need to recognize the limited nature of involvement that may result and the impact this would have on the evidence base. Researchers will need to recognize the resource implications of involvement at this point, and user groups will need to decide whether to participate when there is the greatest chance of influencing research but little or no funding.

Indexed as

Cooperative BehaviorPatient SelectionPremature BirthResearch DesignResearch Support as TopicAdvisory CommitteesBiomedical ResearchFemaleHealth Services AccessibilityHumansInfant, NewbornInterprofessional RelationsMotivationParentsPregnancyProfessional-Patient Relations

Identifiers

PMID17524010
PMCPMC5060394

What OpenQuestion holds

Textmetadata
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.