2014
DOI: 10.1136/jfprhc-2014-101007
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A tool to improve patient and public engagement in commissioning sexual and reproductive health and HIV services

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Cited by 12 publications
(23 citation statements)
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“…Patient engagement can improve the relevance of research to patients, increase uptake of results, and facilitate knowledge translation in concerned communities. [48][49][50][51][52][53] As such, four MLWH living in Canada were engaged in this review as stakeholders. The MLWH included a refugee from Africa, an asylum seeker from Africa, an international student from Asia, and an international student from Western Europe.…”
Section: Patient Engagement In Researchmentioning
confidence: 99%
“…Patient engagement can improve the relevance of research to patients, increase uptake of results, and facilitate knowledge translation in concerned communities. [48][49][50][51][52][53] As such, four MLWH living in Canada were engaged in this review as stakeholders. The MLWH included a refugee from Africa, an asylum seeker from Africa, an international student from Asia, and an international student from Western Europe.…”
Section: Patient Engagement In Researchmentioning
confidence: 99%
“…10 In part, this may stem from limited advice about how to translate general PPI guidance into appropriate practices within SRH, where stigma and need for privacy may mitigate against visible involvement. [11][12][13] Particularly remarkable is lack of attention to the specific challenges of involving young people (hereafter referred to as YP) in SRH-related PPI -a surprising absence given that this age group continues to experience a high burden of poor sexual health outcomes, 14 15 and may be especially susceptible to power differentials within PPI. Opportunities to advance practice are further constrained by limited publication; despite initiatives to increase the visibility of SRH-related PPI, 16 the category for submission of articles focused on involvement often remains unclear, and likely only a fraction of PPI is "written up".…”
Section: How This Study Might Affect Research Practice or Policymentioning
confidence: 99%
“…To this end, standards have been developed on how patient and public involvement in research and clinical services have been developed, alongside efforts to audit the level of patient and public involvement in the delivery of clinical STIs services. [56][57][58][59] A series of audits on patient and public involvement plans in the United Kingdom had demonstrated how understandings of patient and public involvement varied across units, lacked goals, and were limited in their depth of soliciting participation. 60…”
Section: Wwwpublishcsiroau/shmentioning
confidence: 99%