Study Protocol: Phase III single-blinded fast-track pragmatic randomised controlled trial of a complex intervention for breathlessness in advanced disease

<p>Abstract</p> <p>Background</p> <p>Breathlessness in advanced disease causes significant distress to patients and carers and presents management challenges to health care professionals. The Breathlessness Intervention Service (BIS) seeks to improve the care of breathl...

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Main Authors: Brafman-Kennedy Barbara, Gray Jennifer, Higginson Irene J, McCrone Paul, Prevost A Toby, Farquhar Morag C, Booth Sara
Format: Article
Language:English
Published: BMC 2011-05-01
Series:Trials
Online Access:http://www.trialsjournal.com/content/12/1/130
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author Brafman-Kennedy Barbara
Gray Jennifer
Higginson Irene J
McCrone Paul
Prevost A Toby
Farquhar Morag C
Booth Sara
author_facet Brafman-Kennedy Barbara
Gray Jennifer
Higginson Irene J
McCrone Paul
Prevost A Toby
Farquhar Morag C
Booth Sara
author_sort Brafman-Kennedy Barbara
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Breathlessness in advanced disease causes significant distress to patients and carers and presents management challenges to health care professionals. The Breathlessness Intervention Service (BIS) seeks to improve the care of breathless patients with advanced disease (regardless of cause) through the use of evidence-based practice and working with other healthcare providers. BIS delivers a complex intervention (of non-pharmacological and pharmacological treatments) via a multi-professional team. BIS is being continuously developed and its impact evaluated using the MRC's framework for complex interventions (PreClinical, Phase I and Phase II completed). This paper presents the protocol for Phase III.</p> <p>Methods/Design</p> <p>Phase III comprises a pragmatic, fast-track, single-blind randomised controlled trial of BIS versus standard care. Due to differing disease trajectories, the service uses two broad service models: one for patients with malignant disease (intervention delivered over two weeks) and one for patients with non-malignant disease (intervention delivered over four weeks). The Phase III trial therefore consists of two sub-protocols: one for patients with malignant conditions (four week protocol) and one for patients with non-malignant conditions (eight week protocol). Mixed method interviews are conducted with patients and their lay carers at three to five measurement points depending on randomisation and sub-protocol. Qualitative interviews are conducted with referring and non-referring health care professionals (malignant disease protocol only). The primary outcome measure is 'patient distress due to breathlessness' measured on a numerical rating scale (0-10). The trial includes economic evaluation. Analysis will be on an intention to treat basis.</p> <p>Discussion</p> <p>This is the first evaluation of a breathlessness intervention for advanced disease to have followed the MRC framework and one of the first palliative care trials to use fast track methodology and single-blinding. The results will provide evidence of the clinical and cost-effectiveness of the service, informing its longer term development and implementation of the model in other centres nationally and internationally. It adds to methodological developments in palliative care research where complex interventions are common but evidence sparse.</p> <p>Trial Registration</p> <p>ClinicalTrials.gov: <a href="http://www.clinicaltrials.gov/ct2/show/NCT00678405">NCT00678405</a></p> <p>ISRCTN: <a href="http://www.controlled-trials.com/ISRCTN04119516">ISRCTN04119516</a></p>
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spelling doaj.art-94acd030c1454bba813a196d228a98952022-12-22T01:02:30ZengBMCTrials1745-62152011-05-0112113010.1186/1745-6215-12-130Study Protocol: Phase III single-blinded fast-track pragmatic randomised controlled trial of a complex intervention for breathlessness in advanced diseaseBrafman-Kennedy BarbaraGray JenniferHigginson Irene JMcCrone PaulPrevost A TobyFarquhar Morag CBooth Sara<p>Abstract</p> <p>Background</p> <p>Breathlessness in advanced disease causes significant distress to patients and carers and presents management challenges to health care professionals. The Breathlessness Intervention Service (BIS) seeks to improve the care of breathless patients with advanced disease (regardless of cause) through the use of evidence-based practice and working with other healthcare providers. BIS delivers a complex intervention (of non-pharmacological and pharmacological treatments) via a multi-professional team. BIS is being continuously developed and its impact evaluated using the MRC's framework for complex interventions (PreClinical, Phase I and Phase II completed). This paper presents the protocol for Phase III.</p> <p>Methods/Design</p> <p>Phase III comprises a pragmatic, fast-track, single-blind randomised controlled trial of BIS versus standard care. Due to differing disease trajectories, the service uses two broad service models: one for patients with malignant disease (intervention delivered over two weeks) and one for patients with non-malignant disease (intervention delivered over four weeks). The Phase III trial therefore consists of two sub-protocols: one for patients with malignant conditions (four week protocol) and one for patients with non-malignant conditions (eight week protocol). Mixed method interviews are conducted with patients and their lay carers at three to five measurement points depending on randomisation and sub-protocol. Qualitative interviews are conducted with referring and non-referring health care professionals (malignant disease protocol only). The primary outcome measure is 'patient distress due to breathlessness' measured on a numerical rating scale (0-10). The trial includes economic evaluation. Analysis will be on an intention to treat basis.</p> <p>Discussion</p> <p>This is the first evaluation of a breathlessness intervention for advanced disease to have followed the MRC framework and one of the first palliative care trials to use fast track methodology and single-blinding. The results will provide evidence of the clinical and cost-effectiveness of the service, informing its longer term development and implementation of the model in other centres nationally and internationally. It adds to methodological developments in palliative care research where complex interventions are common but evidence sparse.</p> <p>Trial Registration</p> <p>ClinicalTrials.gov: <a href="http://www.clinicaltrials.gov/ct2/show/NCT00678405">NCT00678405</a></p> <p>ISRCTN: <a href="http://www.controlled-trials.com/ISRCTN04119516">ISRCTN04119516</a></p>http://www.trialsjournal.com/content/12/1/130
spellingShingle Brafman-Kennedy Barbara
Gray Jennifer
Higginson Irene J
McCrone Paul
Prevost A Toby
Farquhar Morag C
Booth Sara
Study Protocol: Phase III single-blinded fast-track pragmatic randomised controlled trial of a complex intervention for breathlessness in advanced disease
Trials
title Study Protocol: Phase III single-blinded fast-track pragmatic randomised controlled trial of a complex intervention for breathlessness in advanced disease
title_full Study Protocol: Phase III single-blinded fast-track pragmatic randomised controlled trial of a complex intervention for breathlessness in advanced disease
title_fullStr Study Protocol: Phase III single-blinded fast-track pragmatic randomised controlled trial of a complex intervention for breathlessness in advanced disease
title_full_unstemmed Study Protocol: Phase III single-blinded fast-track pragmatic randomised controlled trial of a complex intervention for breathlessness in advanced disease
title_short Study Protocol: Phase III single-blinded fast-track pragmatic randomised controlled trial of a complex intervention for breathlessness in advanced disease
title_sort study protocol phase iii single blinded fast track pragmatic randomised controlled trial of a complex intervention for breathlessness in advanced disease
url http://www.trialsjournal.com/content/12/1/130
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