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Profiling trial burden and patients’ attitudes to improve clinical research in epidermolysis bullosa

BACKGROUND: Epidermolysis bullosa (EB) comprises inherited mechanobullous dermatoses with considerable morbidity and mortality. While current treatments are symptomatic, a growing number of innovative therapeutic compounds are evaluated in clinical trials. Clinical research in rare diseases like EB,...

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Autores principales: Prodinger, Christine, Diem, Anja, Ude-Schoder, Katherina, Piñón-Hofbauer, Josefina, Kitzmueller, Sophie, Bauer, Johann W., Laimer, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7350741/
https://www.ncbi.nlm.nih.gov/pubmed/32650809
http://dx.doi.org/10.1186/s13023-020-01443-3
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author Prodinger, Christine
Diem, Anja
Ude-Schoder, Katherina
Piñón-Hofbauer, Josefina
Kitzmueller, Sophie
Bauer, Johann W.
Laimer, Martin
author_facet Prodinger, Christine
Diem, Anja
Ude-Schoder, Katherina
Piñón-Hofbauer, Josefina
Kitzmueller, Sophie
Bauer, Johann W.
Laimer, Martin
author_sort Prodinger, Christine
collection PubMed
description BACKGROUND: Epidermolysis bullosa (EB) comprises inherited mechanobullous dermatoses with considerable morbidity and mortality. While current treatments are symptomatic, a growing number of innovative therapeutic compounds are evaluated in clinical trials. Clinical research in rare diseases like EB, however, faces many challenges, including sample size requirements and recruitment failures. The objective of this study was to determine attitudes of EB patients towards clinical research and trial participation as well as the assessment of contextual motivating and discouraging factors in an effort to support patient-centered RD trial designing. METHODS: A 53-items questionnaire was handed over to EB patients (of all types and ages) in contact with the EB House Austria, a designated national center of expertise for EB care. Main categories included level of interest in and personal knowledge about clinical studies, pros/cons for participation and extent of individual expenses considered acceptable for participation in a clinical study. Descriptive subgroup analysis was calculated with SPSS 20.0 and Microsoft Excel. RESULTS: Thirty-six individuals (mean age 25.7 years), diagnosed for recessive dystrophic EB (36.1%), EB simplex (33.4%), junctional EB (8.3%), dominant dystrophic EB (2.8%) and acral peeling syndrome (2.8%) participated. Motivation for participation in and the desire to increase personal knowledge about clinical trials were (outmost) high in 57.2 and 66.7%, respectively. Altruism was the major motivating factor, followed by hope that alleviation of the own symptoms can be achieved. The greatest hurdle was travel distance, followed by concerns about possible adverse reactions. Patients diagnosed for severe subgroups (RDEB, JEB) were more impaired by the extent of scheduled invasive investigations and possible adverse reactions of the study medication. Patients with generally milder EB forms and older patients were accepting more frequent outpatient study visits, blood takes, skin biopsies and inpatient admissions in association with trial participation. CONCLUSIONS: This study provides additional indications to better determine and address attitudes towards clinical research among EB patients as well as guidance to improve clinical trial protocols for patient centricity.
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spelling pubmed-73507412020-07-14 Profiling trial burden and patients’ attitudes to improve clinical research in epidermolysis bullosa Prodinger, Christine Diem, Anja Ude-Schoder, Katherina Piñón-Hofbauer, Josefina Kitzmueller, Sophie Bauer, Johann W. Laimer, Martin Orphanet J Rare Dis Research BACKGROUND: Epidermolysis bullosa (EB) comprises inherited mechanobullous dermatoses with considerable morbidity and mortality. While current treatments are symptomatic, a growing number of innovative therapeutic compounds are evaluated in clinical trials. Clinical research in rare diseases like EB, however, faces many challenges, including sample size requirements and recruitment failures. The objective of this study was to determine attitudes of EB patients towards clinical research and trial participation as well as the assessment of contextual motivating and discouraging factors in an effort to support patient-centered RD trial designing. METHODS: A 53-items questionnaire was handed over to EB patients (of all types and ages) in contact with the EB House Austria, a designated national center of expertise for EB care. Main categories included level of interest in and personal knowledge about clinical studies, pros/cons for participation and extent of individual expenses considered acceptable for participation in a clinical study. Descriptive subgroup analysis was calculated with SPSS 20.0 and Microsoft Excel. RESULTS: Thirty-six individuals (mean age 25.7 years), diagnosed for recessive dystrophic EB (36.1%), EB simplex (33.4%), junctional EB (8.3%), dominant dystrophic EB (2.8%) and acral peeling syndrome (2.8%) participated. Motivation for participation in and the desire to increase personal knowledge about clinical trials were (outmost) high in 57.2 and 66.7%, respectively. Altruism was the major motivating factor, followed by hope that alleviation of the own symptoms can be achieved. The greatest hurdle was travel distance, followed by concerns about possible adverse reactions. Patients diagnosed for severe subgroups (RDEB, JEB) were more impaired by the extent of scheduled invasive investigations and possible adverse reactions of the study medication. Patients with generally milder EB forms and older patients were accepting more frequent outpatient study visits, blood takes, skin biopsies and inpatient admissions in association with trial participation. CONCLUSIONS: This study provides additional indications to better determine and address attitudes towards clinical research among EB patients as well as guidance to improve clinical trial protocols for patient centricity. BioMed Central 2020-07-10 /pmc/articles/PMC7350741/ /pubmed/32650809 http://dx.doi.org/10.1186/s13023-020-01443-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research
Prodinger, Christine
Diem, Anja
Ude-Schoder, Katherina
Piñón-Hofbauer, Josefina
Kitzmueller, Sophie
Bauer, Johann W.
Laimer, Martin
Profiling trial burden and patients’ attitudes to improve clinical research in epidermolysis bullosa
title Profiling trial burden and patients’ attitudes to improve clinical research in epidermolysis bullosa
title_full Profiling trial burden and patients’ attitudes to improve clinical research in epidermolysis bullosa
title_fullStr Profiling trial burden and patients’ attitudes to improve clinical research in epidermolysis bullosa
title_full_unstemmed Profiling trial burden and patients’ attitudes to improve clinical research in epidermolysis bullosa
title_short Profiling trial burden and patients’ attitudes to improve clinical research in epidermolysis bullosa
title_sort profiling trial burden and patients’ attitudes to improve clinical research in epidermolysis bullosa
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7350741/
https://www.ncbi.nlm.nih.gov/pubmed/32650809
http://dx.doi.org/10.1186/s13023-020-01443-3
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