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Researchers Attitudes to Public Involvement in Health Research

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Understanding health researchers' attitudes may help to ... Ticking boxes? ... that very often genuine attempts to, almost like ticking the box if you like. ... – PowerPoint PPT presentation

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Title: Researchers Attitudes to Public Involvement in Health Research


1
Researchers Attitudes to Public Involvement in
Health Research
  • Jill Thompson Jonathan Boote
  • Rosemary Barber Chris Armitage
  • Cindy Cooper Georgina Jones
  • Paul Ward

2
Why?
  • Difference between rhetoric and reality
  • Understanding health researchers attitudes may
    help to explain why policy is not more
    widespread.
  • Directions for the future.

3
How?
  • 15 semi-structured interviews
  • University Researchers
  • Health Research Clinical Trials, Health Services
    Research and Biomedical Science

4
Findings
5
Competing Constructions
  • Co-researchers
  • Public engagement
  • By proxy
  • Well, I mean Im a GP so I am sitting listening
    to what patients are telling me every day.
  • (Health Service Researcher 7)

6
Apprehension
  • Fear of the unknown
  • Its a different way of working. Its
    uncomfortable to move out of your set ways.
  • (Health Service Researcher 3)
  • youre not quite sure what the threat is, but
    suddenly you feel exposed, you were hiding behind
    your title or your authority
  • (Health Service Researcher 1)

7
  • Threat to professional skills and academic
    knowledge
  • I think there is definitely a thing about people
    feeling slightly threatened, researchers feeling
    threatened in terms of their own expertise and
    skills.
  • (Health Service Researcher 4)
  • and suddenly they are the experts and they have
    done no studying, no qualifications and I think
    that she feels a bit kind of like, thats not
    right.
  • (Health Service Researcher 8)

8
Belief Differences
  • there may be conflicting interests where the
    patient agenda differs very much from perhaps
    what the clinicians, in some senses may want to
    look at.
  • (Health Service Researcher 3)
  • patients will by definition often bring their
    own personalised agenda.
  • (Clinical Trials 1)

9
Appropriate People
  • Representativeness
  • I also think that it is very difficult to find a
    member of the public who are truly representative
    of their communities and the public.
  • (Health Service Researcher 10)
  • Professional Patient
  • theres an argument about when service users go
    from, become professionalised, thats the
    problem of losing your grass roots credibility.
  • (Health Service Researcher 2)

10
Value
  • Validation
  • It makes it better because they could get
    information that we couldnt nearly so easily.
  • (Health Service Researcher 3)
  • Transparency
  • Unique point of view

11
Ethical Obligation
  • Tax
  • ..its their money in terms of taxes
  • (Health Service Researcher 6)
  • Targeted towards need
  • I would hope that it would produce better
    resaerch, research that is more relevant and more
    pertinent to peoples real needs
  • (Health Service Researcher 4)

12
Political Imperative
  • Funding, governance and ethics applications
  • Ticking boxes?
  • there is a lot of lip service paid to this and
    erm, I dont think that very often genuine
    attempts to, almost like ticking the box if you
    like. Have you involved the public? Yes
  • (Health Service Researcher 9)

13
Concluding thoughts
  • Does service user involvement challenge our ideas
    about valid and acceptable knowledge?
  • Is research governance effective in promoting
    public involvement in research?
  • The way forward?
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