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Assessing the feasibility of injectable growth-promoting therapy in Crohn’s disease
BACKGROUND: Despite optimal therapy, many children with Crohn’s disease (CD) experience growth retardation. The objectives of the study are to assess the feasibility of a randomised control trial (RCT) of injectable forms of growth-promoting therapy and to survey the attitudes of children with CD an...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153677/ https://www.ncbi.nlm.nih.gov/pubmed/27965886 http://dx.doi.org/10.1186/s40814-016-0112-9 |
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author | Altowati, Mabrouka A. Jones, Ashley P. Hickey, Helen Williamson, Paula R. Barakat, Farah M. Plaatjies, Nicolene C. Hardwick, Ben Russell, Richard K. Jaki, Thomas Ahmed, S. Faisal Sanderson, Ian R. |
author_facet | Altowati, Mabrouka A. Jones, Ashley P. Hickey, Helen Williamson, Paula R. Barakat, Farah M. Plaatjies, Nicolene C. Hardwick, Ben Russell, Richard K. Jaki, Thomas Ahmed, S. Faisal Sanderson, Ian R. |
author_sort | Altowati, Mabrouka A. |
collection | PubMed |
description | BACKGROUND: Despite optimal therapy, many children with Crohn’s disease (CD) experience growth retardation. The objectives of the study are to assess the feasibility of a randomised control trial (RCT) of injectable forms of growth-promoting therapy and to survey the attitudes of children with CD and their parents to it. METHODS: A feasibility study was carried out to determine study arms, sample size and numbers of eligible patients. A face-to-face questionnaire surveyed willingness to consent to future participation in the RCT. Eligibility to the survey was any child under 18 (with their parent/guardian) with CD whose height standard deviation score (HtSDS) was ≤+1. Of 118 questionnaires, 94 (80%) were returned (48 by children and 46 by parents). RESULTS: The median age of the patients in the survey was 14.3 years (range 7.0 to 17.7), and 35 (73%) were male. Their median HtSDS was −1.2 (−3.01, 0.23), and it was lower than the median mid-parental HtSDS of −0.6 (−3.1, 1.4). We analysed the willingness of the children whose HtSDS <−1 to take part in the proposed RCT, being those most likely to require treatment. Overall, 18 (47%) children and 17 (46%) parents were willing. This increased to 61% of children who were slightly concerned about their height and 100% (4/4) of those very concerned. A common reason for not taking part in the RCT was fear of injections (44%); 111 children are required for randomisation into three study arms from nine centres. CONCLUSIONS: Almost half of children and parents surveyed would take part in an RCT of growth-promoting therapy. Allaying fears about injections may result in higher recruitment rates. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40814-016-0112-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5153677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-51536772016-12-13 Assessing the feasibility of injectable growth-promoting therapy in Crohn’s disease Altowati, Mabrouka A. Jones, Ashley P. Hickey, Helen Williamson, Paula R. Barakat, Farah M. Plaatjies, Nicolene C. Hardwick, Ben Russell, Richard K. Jaki, Thomas Ahmed, S. Faisal Sanderson, Ian R. Pilot Feasibility Stud Research BACKGROUND: Despite optimal therapy, many children with Crohn’s disease (CD) experience growth retardation. The objectives of the study are to assess the feasibility of a randomised control trial (RCT) of injectable forms of growth-promoting therapy and to survey the attitudes of children with CD and their parents to it. METHODS: A feasibility study was carried out to determine study arms, sample size and numbers of eligible patients. A face-to-face questionnaire surveyed willingness to consent to future participation in the RCT. Eligibility to the survey was any child under 18 (with their parent/guardian) with CD whose height standard deviation score (HtSDS) was ≤+1. Of 118 questionnaires, 94 (80%) were returned (48 by children and 46 by parents). RESULTS: The median age of the patients in the survey was 14.3 years (range 7.0 to 17.7), and 35 (73%) were male. Their median HtSDS was −1.2 (−3.01, 0.23), and it was lower than the median mid-parental HtSDS of −0.6 (−3.1, 1.4). We analysed the willingness of the children whose HtSDS <−1 to take part in the proposed RCT, being those most likely to require treatment. Overall, 18 (47%) children and 17 (46%) parents were willing. This increased to 61% of children who were slightly concerned about their height and 100% (4/4) of those very concerned. A common reason for not taking part in the RCT was fear of injections (44%); 111 children are required for randomisation into three study arms from nine centres. CONCLUSIONS: Almost half of children and parents surveyed would take part in an RCT of growth-promoting therapy. Allaying fears about injections may result in higher recruitment rates. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40814-016-0112-9) contains supplementary material, which is available to authorized users. BioMed Central 2016-12-05 /pmc/articles/PMC5153677/ /pubmed/27965886 http://dx.doi.org/10.1186/s40814-016-0112-9 Text en © The Author(s). 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 | Research Altowati, Mabrouka A. Jones, Ashley P. Hickey, Helen Williamson, Paula R. Barakat, Farah M. Plaatjies, Nicolene C. Hardwick, Ben Russell, Richard K. Jaki, Thomas Ahmed, S. Faisal Sanderson, Ian R. Assessing the feasibility of injectable growth-promoting therapy in Crohn’s disease |
title | Assessing the feasibility of injectable growth-promoting therapy in Crohn’s disease |
title_full | Assessing the feasibility of injectable growth-promoting therapy in Crohn’s disease |
title_fullStr | Assessing the feasibility of injectable growth-promoting therapy in Crohn’s disease |
title_full_unstemmed | Assessing the feasibility of injectable growth-promoting therapy in Crohn’s disease |
title_short | Assessing the feasibility of injectable growth-promoting therapy in Crohn’s disease |
title_sort | assessing the feasibility of injectable growth-promoting therapy in crohn’s disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153677/ https://www.ncbi.nlm.nih.gov/pubmed/27965886 http://dx.doi.org/10.1186/s40814-016-0112-9 |
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