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Bridie Fitzpatrick

Biographic Data

ID6164587
NAMEBridie Fitzpatrick
GIVEN NAMESBridie
FAMILY NAMEFitzpatrick
SIGNATUREFITZPATRICK B
AFFILIATIONSUniversity of Glasgow
ORCID0000-0002-1806-8738
VERIFIEDYes
TOTAL WORKS3
TOTAL CITATIONS4
WORKS AS AUTHOR3
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2005
LATEST PUBLICATION YEAR2018
H-INDEX1
  • Partnership approaches to the evaluation of complex policy initiatives

    Open Access•Fiona Turner‐halliday, Vicki Welch et al.•ARTICLE•International Journal of Social…•2018•Cited by: 1•References: 4

    We argue that major health and social care policy initiatives are not too complex for randomised controlled trial (RCT) methodology and illustrate this using the example of the Best Services Trial (BeST ? ): a RCT of an infant mental health intervention for maltreated children. We suggest that qualitative research, as a core part of the trial process from conception and development through to implementation and evaluation, is crucial in building,…

  • Randomisation before consent

    Vicki Welch, Fiona Turner-Halliday et al.•ARTICLE•International Journal of Social…•2016•Cited by: 3•References: 9

    Obtaining informed consent can be challenging in stressful and urgent circumstances. One example is when potential participants have recently had their child removed into care; intervention is urgent and mandatory whereas participation in associated research is voluntary. Using a nested qualitative study, we examined experiences of consent processes in a randomised controlled trial of a family assessment and intervention service for maltreated yo…

  • Can we evaluate population screening strategies in UK general practice? A pilot randomised controlled trial comparing postal and opportunistic screening for genital chlamydial infection

    Abiola Senok, Philip Wilson et al.•ARTICLE•Journal of Epidemiology and…•2005•References: 17

    Study objective: To assess whether opportunistic and postal screening strategies for Chlamydia trachomatis can be compared with usual care in a randomised trial in general practice. Design: Feasibility study for a randomised controlled trial. Setting: Three West of Scotland general medical practices: one rural, one urban/deprived, and one urban/affluent. Participants: 600 women aged 16–30 years, 200 from each of three participating practices sele…

  • Randomisation before consent

    Vicki Welch, Fiona Turner-Halliday et al.•ARTICLE•International Journal of Social…•2016•Cited by: 3•References: 9

    Obtaining informed consent can be challenging in stressful and urgent circumstances. One example is when potential participants have recently had their child removed into care; intervention is urgent and mandatory whereas participation in associated research is voluntary. Using a nested qualitative study, we examined experiences of consent processes in a randomised controlled trial of a family assessment and intervention service for maltreated yo…

  • Partnership approaches to the evaluation of complex policy initiatives

    Open Access•Fiona Turner‐halliday, Vicki Welch et al.•ARTICLE•International Journal of Social…•2018•Cited by: 1•References: 4

    We argue that major health and social care policy initiatives are not too complex for randomised controlled trial (RCT) methodology and illustrate this using the example of the Best Services Trial (BeST ? ): a RCT of an infant mental health intervention for maltreated children. We suggest that qualitative research, as a core part of the trial process from conception and development through to implementation and evaluation, is crucial in building,…

  • Can we evaluate population screening strategies in UK general practice? A pilot randomised controlled trial comparing postal and opportunistic screening for genital chlamydial infection

    Abiola Senok, Philip Wilson et al.•ARTICLE•Journal of Epidemiology and…•2005•References: 17

    Study objective: To assess whether opportunistic and postal screening strategies for Chlamydia trachomatis can be compared with usual care in a randomised trial in general practice. Design: Feasibility study for a randomised controlled trial. Setting: Three West of Scotland general medical practices: one rural, one urban/deprived, and one urban/affluent. Participants: 600 women aged 16–30 years, 200 from each of three participating practices sele…

  • Randomisation before consent

    Vicki Welch, Fiona Turner-Halliday et al.•ARTICLE•International Journal of Social…•2016•Cited by: 3•References: 9

    Obtaining informed consent can be challenging in stressful and urgent circumstances. One example is when potential participants have recently had their child removed into care; intervention is urgent and mandatory whereas participation in associated research is voluntary. Using a nested qualitative study, we examined experiences of consent processes in a randomised controlled trial of a family assessment and intervention service for maltreated yo…

  • Partnership approaches to the evaluation of complex policy initiatives

    Open Access•Fiona Turner‐halliday, Vicki Welch et al.•ARTICLE•International Journal of Social…•2018•Cited by: 1•References: 4

    We argue that major health and social care policy initiatives are not too complex for randomised controlled trial (RCT) methodology and illustrate this using the example of the Best Services Trial (BeST ? ): a RCT of an infant mental health intervention for maltreated children. We suggest that qualitative research, as a core part of the trial process from conception and development through to implementation and evaluation, is crucial in building,…

Medicine (3 works) · Randomized controlled trial (3 works) · Child Abuse and Trauma (2 works) · Family medicine (2 works) · Mental Health and Patient Involvement (2 works) · Nursing (2 works) · Psychological intervention (2 works) · Psychology (2 works) · Qualitative research (2 works) · Alternative medicine (1 work)

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