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Progressive postresection program (pPRP) after pancreatic resection: study protocol for a randomized controlled trial

BACKGROUND: At the time of initial diagnosis, only 15–20 % of patients with pancreatic cancer present with a resectable disease. Patients with pancreatic cancer face a poor prognosis. Progression-free survival and overall survival rates are very limited, so it is important to develop concepts to imp...

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Autores principales: Richter, Susanne, Uslar, Verena, Tabriz, Navid, Mueser, Thomas, Weyhe, Dirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4750352/
https://www.ncbi.nlm.nih.gov/pubmed/26863867
http://dx.doi.org/10.1186/s13063-016-1200-0
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author Richter, Susanne
Uslar, Verena
Tabriz, Navid
Mueser, Thomas
Weyhe, Dirk
author_facet Richter, Susanne
Uslar, Verena
Tabriz, Navid
Mueser, Thomas
Weyhe, Dirk
author_sort Richter, Susanne
collection PubMed
description BACKGROUND: At the time of initial diagnosis, only 15–20 % of patients with pancreatic cancer present with a resectable disease. Patients with pancreatic cancer face a poor prognosis. Progression-free survival and overall survival rates are very limited, so it is important to develop concepts to improve the quality of life for their remaining lives. METHODS/DESIGN: The proposed trial is a randomized controlled intervention study. After pancreatic resection, the intervention group (cohort A, n = 30 patients) will take part in an intensified physiotherapy program consisting of endurance and muscle force exercises. The control group (cohort B, n = 30 patients) will take part in standard physiotherapy. Both groups will receive dietary counseling and, if necessary, substitution for endocrine/exocrine pancreatic insufficiency. Quality of life will be evaluated using the Short Form-8 Health Survey and the European Organization for Research and Treatment of Cancer QLQ-C30/QLQ-PAN26 questionnaires. DISCUSSION: The aim of this study is to investigate whether intensive physiotherapy improves the quality of life of patients after pancreatic resection. If the results for the intervention group are positive, a multicenter study should be performed with appropriate statistical power. The progressive postresection program includes a structured follow-up after pancreatic resection. In this study, all patients will undergo abdominal computed tomography for follow-up 6 and 12 months postoperatively. TRIAL REGISTRATION: German Clinical Trials Register DRKS00006786. Date of registration 1 October 2014.
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spelling pubmed-47503522016-02-12 Progressive postresection program (pPRP) after pancreatic resection: study protocol for a randomized controlled trial Richter, Susanne Uslar, Verena Tabriz, Navid Mueser, Thomas Weyhe, Dirk Trials Study Protocol BACKGROUND: At the time of initial diagnosis, only 15–20 % of patients with pancreatic cancer present with a resectable disease. Patients with pancreatic cancer face a poor prognosis. Progression-free survival and overall survival rates are very limited, so it is important to develop concepts to improve the quality of life for their remaining lives. METHODS/DESIGN: The proposed trial is a randomized controlled intervention study. After pancreatic resection, the intervention group (cohort A, n = 30 patients) will take part in an intensified physiotherapy program consisting of endurance and muscle force exercises. The control group (cohort B, n = 30 patients) will take part in standard physiotherapy. Both groups will receive dietary counseling and, if necessary, substitution for endocrine/exocrine pancreatic insufficiency. Quality of life will be evaluated using the Short Form-8 Health Survey and the European Organization for Research and Treatment of Cancer QLQ-C30/QLQ-PAN26 questionnaires. DISCUSSION: The aim of this study is to investigate whether intensive physiotherapy improves the quality of life of patients after pancreatic resection. If the results for the intervention group are positive, a multicenter study should be performed with appropriate statistical power. The progressive postresection program includes a structured follow-up after pancreatic resection. In this study, all patients will undergo abdominal computed tomography for follow-up 6 and 12 months postoperatively. TRIAL REGISTRATION: German Clinical Trials Register DRKS00006786. Date of registration 1 October 2014. BioMed Central 2016-02-10 /pmc/articles/PMC4750352/ /pubmed/26863867 http://dx.doi.org/10.1186/s13063-016-1200-0 Text en © Richter et al. 2016 Open AccessThis 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.
spellingShingle Study Protocol
Richter, Susanne
Uslar, Verena
Tabriz, Navid
Mueser, Thomas
Weyhe, Dirk
Progressive postresection program (pPRP) after pancreatic resection: study protocol for a randomized controlled trial
title Progressive postresection program (pPRP) after pancreatic resection: study protocol for a randomized controlled trial
title_full Progressive postresection program (pPRP) after pancreatic resection: study protocol for a randomized controlled trial
title_fullStr Progressive postresection program (pPRP) after pancreatic resection: study protocol for a randomized controlled trial
title_full_unstemmed Progressive postresection program (pPRP) after pancreatic resection: study protocol for a randomized controlled trial
title_short Progressive postresection program (pPRP) after pancreatic resection: study protocol for a randomized controlled trial
title_sort progressive postresection program (pprp) after pancreatic resection: study protocol for a randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4750352/
https://www.ncbi.nlm.nih.gov/pubmed/26863867
http://dx.doi.org/10.1186/s13063-016-1200-0
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