Cargando…

The serious mental illness health improvement profile [HIP]: study protocol for a cluster randomised controlled trial

BACKGROUND: The serious mental illness Health Improvement Profile [HIP] is a brief pragmatic tool, which enables mental health nurses to work together with patients to screen physical health and take evidence-based action when variables are identified to be at risk. Piloting has demonstrated clinica...

Descripción completa

Detalles Bibliográficos
Autores principales: White, Jacquie, Gray, Richard J, Swift, Louise, Barton, Garry R, Jones, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3148991/
https://www.ncbi.nlm.nih.gov/pubmed/21726440
http://dx.doi.org/10.1186/1745-6215-12-167
_version_ 1782209400365121536
author White, Jacquie
Gray, Richard J
Swift, Louise
Barton, Garry R
Jones, Martin
author_facet White, Jacquie
Gray, Richard J
Swift, Louise
Barton, Garry R
Jones, Martin
author_sort White, Jacquie
collection PubMed
description BACKGROUND: The serious mental illness Health Improvement Profile [HIP] is a brief pragmatic tool, which enables mental health nurses to work together with patients to screen physical health and take evidence-based action when variables are identified to be at risk. Piloting has demonstrated clinical utility and acceptability. METHODS/DESIGN: A single blind parallel group cluster randomised controlled trial with secondary economic analysis and process observation. Unit of randomisation: mental health nurses [MHNs] working in adult community mental health teams across two NHS Trusts. Subjects: Patients over 18 years with a diagnosis of schizophrenia, schizoaffective or bipolar disorder on the caseload of participating MHNs. Primary objective: To determine the effects of the HIP programme on patients' physical wellbeing assessed by the physical component score of the Medical Outcome Study (MOS) 36 Item Short Form Health Survey version 2 [SF-36v2]. Secondary objectives: To determine the effects of the HIP programme on: cost effectiveness, mental wellbeing, cardiovascular risk, physical health care attitudes and knowledge of MHNs and to determine the acceptability of the HIP Programme in the NHS. Consented nurses (and patients) will be randomised to receive the HIP Programme or treatment as usual. Outcomes will be measured at baseline and 12 months with a process observation after 12 months to include evaluation of patients' and professionals' experience and observation of any effect on care plans and primary-secondary care interface communication. Outcomes will be analysed on an intention-to-treat (ITT) basis. DISCUSSION: The results of the trial and process observation will provide information about the effectiveness of the HIP Programme in supporting MHNs to address physical comorbidity in serious mental illness. Given the current unacceptable prevalence of physical comorbidity and mortality in the serious mental illness population, it is hoped the HIP trial will provide a timely contribution to evidence on organisation and delivery of care for patients, clinicians and policy makers. TRIAL REGISTRATION: ISRCTN: ISRCTN41137900
format Online
Article
Text
id pubmed-3148991
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-31489912011-08-03 The serious mental illness health improvement profile [HIP]: study protocol for a cluster randomised controlled trial White, Jacquie Gray, Richard J Swift, Louise Barton, Garry R Jones, Martin Trials Study Protocol BACKGROUND: The serious mental illness Health Improvement Profile [HIP] is a brief pragmatic tool, which enables mental health nurses to work together with patients to screen physical health and take evidence-based action when variables are identified to be at risk. Piloting has demonstrated clinical utility and acceptability. METHODS/DESIGN: A single blind parallel group cluster randomised controlled trial with secondary economic analysis and process observation. Unit of randomisation: mental health nurses [MHNs] working in adult community mental health teams across two NHS Trusts. Subjects: Patients over 18 years with a diagnosis of schizophrenia, schizoaffective or bipolar disorder on the caseload of participating MHNs. Primary objective: To determine the effects of the HIP programme on patients' physical wellbeing assessed by the physical component score of the Medical Outcome Study (MOS) 36 Item Short Form Health Survey version 2 [SF-36v2]. Secondary objectives: To determine the effects of the HIP programme on: cost effectiveness, mental wellbeing, cardiovascular risk, physical health care attitudes and knowledge of MHNs and to determine the acceptability of the HIP Programme in the NHS. Consented nurses (and patients) will be randomised to receive the HIP Programme or treatment as usual. Outcomes will be measured at baseline and 12 months with a process observation after 12 months to include evaluation of patients' and professionals' experience and observation of any effect on care plans and primary-secondary care interface communication. Outcomes will be analysed on an intention-to-treat (ITT) basis. DISCUSSION: The results of the trial and process observation will provide information about the effectiveness of the HIP Programme in supporting MHNs to address physical comorbidity in serious mental illness. Given the current unacceptable prevalence of physical comorbidity and mortality in the serious mental illness population, it is hoped the HIP trial will provide a timely contribution to evidence on organisation and delivery of care for patients, clinicians and policy makers. TRIAL REGISTRATION: ISRCTN: ISRCTN41137900 BioMed Central 2011-07-04 /pmc/articles/PMC3148991/ /pubmed/21726440 http://dx.doi.org/10.1186/1745-6215-12-167 Text en Copyright ©2011 White et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Study Protocol
White, Jacquie
Gray, Richard J
Swift, Louise
Barton, Garry R
Jones, Martin
The serious mental illness health improvement profile [HIP]: study protocol for a cluster randomised controlled trial
title The serious mental illness health improvement profile [HIP]: study protocol for a cluster randomised controlled trial
title_full The serious mental illness health improvement profile [HIP]: study protocol for a cluster randomised controlled trial
title_fullStr The serious mental illness health improvement profile [HIP]: study protocol for a cluster randomised controlled trial
title_full_unstemmed The serious mental illness health improvement profile [HIP]: study protocol for a cluster randomised controlled trial
title_short The serious mental illness health improvement profile [HIP]: study protocol for a cluster randomised controlled trial
title_sort serious mental illness health improvement profile [hip]: study protocol for a cluster randomised controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3148991/
https://www.ncbi.nlm.nih.gov/pubmed/21726440
http://dx.doi.org/10.1186/1745-6215-12-167
work_keys_str_mv AT whitejacquie theseriousmentalillnesshealthimprovementprofilehipstudyprotocolforaclusterrandomisedcontrolledtrial
AT grayrichardj theseriousmentalillnesshealthimprovementprofilehipstudyprotocolforaclusterrandomisedcontrolledtrial
AT swiftlouise theseriousmentalillnesshealthimprovementprofilehipstudyprotocolforaclusterrandomisedcontrolledtrial
AT bartongarryr theseriousmentalillnesshealthimprovementprofilehipstudyprotocolforaclusterrandomisedcontrolledtrial
AT jonesmartin theseriousmentalillnesshealthimprovementprofilehipstudyprotocolforaclusterrandomisedcontrolledtrial
AT whitejacquie seriousmentalillnesshealthimprovementprofilehipstudyprotocolforaclusterrandomisedcontrolledtrial
AT grayrichardj seriousmentalillnesshealthimprovementprofilehipstudyprotocolforaclusterrandomisedcontrolledtrial
AT swiftlouise seriousmentalillnesshealthimprovementprofilehipstudyprotocolforaclusterrandomisedcontrolledtrial
AT bartongarryr seriousmentalillnesshealthimprovementprofilehipstudyprotocolforaclusterrandomisedcontrolledtrial
AT jonesmartin seriousmentalillnesshealthimprovementprofilehipstudyprotocolforaclusterrandomisedcontrolledtrial