Show simple item record

dc.contributor.authorBjornstad, G
dc.contributor.authorWilkinson, K
dc.contributor.authorCuffe-Fuller, B
dc.contributor.authorFitzpatrick, K
dc.contributor.authorBorek, A
dc.contributor.authorUkoumunne, OC
dc.contributor.authorHawton, A
dc.contributor.authorTarrant, M
dc.contributor.authorBerry, V
dc.contributor.authorLloyd, J
dc.contributor.authorMcDonald, A
dc.contributor.authorFredlund, M
dc.contributor.authorRhodes, S
dc.contributor.authorLogan, S
dc.contributor.authorMorris, C
dc.date.accessioned2019-11-25T10:19:35Z
dc.date.issued2019-11-23
dc.description.abstractParent carers of disabled children are at increased risk of mental and physical health problems. They often experience challenges to maintaining good health which have implications for their well-being and their ability to care for their children. In response to these needs, researchers and parent carers developed the Healthy Parent Carers (HPC) programme. It is a peer-led, group-based intervention that promotes behaviours associated with health and well-being. The aims of this trial are to assess the acceptability of the HPC programme and the feasibility of its delivery in the community and to assess the feasibility and acceptability of the design of the definitive trial to evaluate the programme’s effectiveness and cost-effectiveness. Methods We will establish six research sites and train facilitators to deliver the manualised intervention. Parent carers of children with special educational needs and disabilities will be individually randomised, stratified by group delivery site, to either take part in a group programme and online resources (intervention) or to receive access to the online resources only (control). Measures of mental health; well-being; health-related quality of life; health behaviours; patient activation; protective factors such as resilience, social connections, and practical support; and use of health care, social care, and wider societal resources will be collected before randomisation (baseline), immediately post-intervention, and 6 months later. Recruitment of participants, adherence to the programme, and the dose received will be assessed. Group sessions will be audio-recorded to evaluate the fidelity of delivery and participant engagement. Participants’ and facilitators’ feedback on the programme content and delivery, their experience, and the acceptability of the outcome measures and trial design will be collected through feedback forms, interviews, and focus groups. Discussion This trial will assess whether the programme delivery and evaluative trial design are feasible, to inform whether to progress to a definitive randomised controlled trial to test the effectiveness and cost-effectiveness of the Healthy Parent Carers programme.en_GB
dc.description.sponsorshipNational Institute for Health Research (NIHR)en_GB
dc.identifier.citationVol. 5, 137en_GB
dc.identifier.doi10.1186/s40814-019-0517-3
dc.identifier.grantnumberPB-PG-0317-20044en_GB
dc.identifier.urihttp://hdl.handle.net/10871/39765
dc.language.isoenen_GB
dc.publisherBMCen_GB
dc.rightsOpen Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.en_GB
dc.subjectBehaviour changeen_GB
dc.subjectwell-beingen_GB
dc.subjectresilienceen_GB
dc.subjectpeer supporten_GB
dc.subjectpatoemt amd public involvementen_GB
dc.subjectdisabled childrenen_GB
dc.subjectparentsen_GB
dc.subjectcarersen_GB
dc.titleHealthy Parent Carers peer-led group-based health promotion intervention for parent carers of disabled children: protocol for a feasibility study using a parallel group randomised controlled trial designen_GB
dc.typeArticleen_GB
dc.date.available2019-11-25T10:19:35Z
exeter.article-number137en_GB
dc.descriptionThis is the final version. Available from BMC via the DOI in this record. en_GB
dc.identifier.eissn2055-5784
dc.identifier.journalPilot and Feasibility Studiesen_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2019-10-15
exeter.funder::National Institute for Health Research (NIHR)en_GB
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2019-11-23
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2019-11-25T10:14:28Z
refterms.versionFCDVoR
refterms.dateFOA2019-11-25T10:19:38Z
refterms.panelAen_GB


Files in this item

This item appears in the following Collection(s)

Show simple item record

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Except where otherwise noted, this item's licence is described as Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.