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Creating a database of internet-based clinical trials to support a public-led research programme: A descriptive analysis
BACKGROUND: Online trials are rapidly growing in number, offering potential benefits but also methodological, ethical and social challenges. The International Network for Knowledge on Well-being (ThinkWell™) aims to increase public and patient participation in the prioritisation, design and conduct...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999056/ https://www.ncbi.nlm.nih.gov/pubmed/29942546 http://dx.doi.org/10.1177/2055207615617854 |
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author | Brice, Anne Price, Amy Burls, Amanda |
author_facet | Brice, Anne Price, Amy Burls, Amanda |
author_sort | Brice, Anne |
collection | PubMed |
description | BACKGROUND: Online trials are rapidly growing in number, offering potential benefits but also methodological, ethical and social challenges. The International Network for Knowledge on Well-being (ThinkWell™) aims to increase public and patient participation in the prioritisation, design and conduct of research through the use of technologies. OBJECTIVE: We aim to provide a baseline understanding of the online trial environment, determining how many trials have used internet-based technologies; how they have been used; and how use has developed over time. METHODS: We searched a range of bibliographic databases to March 2015, with no date limits, supplemented by citation searching and references provided by experts in the field. Results were screened against inclusion and exclusion criteria, and included studies mapped against a number of key dimensions, with key themes developed iteratively throughout the process. RESULTS: We identified 1992 internet-based trials to March 2015. The number of reported studies increased substantially over the study timeframe. The largest number of trials were conducted in the USA (49.7%), followed by The Netherlands (10.2%); Australia (8.5%); the United Kingdom (5.8%); Sweden (4.6%); Canada (4%); and Germany (2.6%). South Korea (1.5%) has the highest number of reported trials for other continents. There is a predominance of interventions addressing core public health challenges including obesity (8.6%), smoking cessation (5.9%), alcohol abuse (7.7%) and physical activity (10.2%); in mental health issues such as depression (10.9%) and anxiety (5.6%); and conditions where self-management (16.6%) or monitoring (8.1%) is a major feature of care. CONCLUSIONS: The results confirm an increase in the use of the internet in trials. Key themes have emerged from the analysis and further research will be undertaken in order to investigate how the data can be used to improve trial design and recruitment, and to build an open access resource to support the public-led research agenda. |
format | Online Article Text |
id | pubmed-5999056 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-59990562018-06-25 Creating a database of internet-based clinical trials to support a public-led research programme: A descriptive analysis Brice, Anne Price, Amy Burls, Amanda Digit Health Original Article BACKGROUND: Online trials are rapidly growing in number, offering potential benefits but also methodological, ethical and social challenges. The International Network for Knowledge on Well-being (ThinkWell™) aims to increase public and patient participation in the prioritisation, design and conduct of research through the use of technologies. OBJECTIVE: We aim to provide a baseline understanding of the online trial environment, determining how many trials have used internet-based technologies; how they have been used; and how use has developed over time. METHODS: We searched a range of bibliographic databases to March 2015, with no date limits, supplemented by citation searching and references provided by experts in the field. Results were screened against inclusion and exclusion criteria, and included studies mapped against a number of key dimensions, with key themes developed iteratively throughout the process. RESULTS: We identified 1992 internet-based trials to March 2015. The number of reported studies increased substantially over the study timeframe. The largest number of trials were conducted in the USA (49.7%), followed by The Netherlands (10.2%); Australia (8.5%); the United Kingdom (5.8%); Sweden (4.6%); Canada (4%); and Germany (2.6%). South Korea (1.5%) has the highest number of reported trials for other continents. There is a predominance of interventions addressing core public health challenges including obesity (8.6%), smoking cessation (5.9%), alcohol abuse (7.7%) and physical activity (10.2%); in mental health issues such as depression (10.9%) and anxiety (5.6%); and conditions where self-management (16.6%) or monitoring (8.1%) is a major feature of care. CONCLUSIONS: The results confirm an increase in the use of the internet in trials. Key themes have emerged from the analysis and further research will be undertaken in order to investigate how the data can be used to improve trial design and recruitment, and to build an open access resource to support the public-led research agenda. SAGE Publications 2015-11-20 /pmc/articles/PMC5999056/ /pubmed/29942546 http://dx.doi.org/10.1177/2055207615617854 Text en © The Author(s) 2015 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Brice, Anne Price, Amy Burls, Amanda Creating a database of internet-based clinical trials to support a public-led research programme: A descriptive analysis |
title | Creating a database of internet-based clinical trials to support a public-led research programme: A descriptive analysis |
title_full | Creating a database of internet-based clinical trials to support a public-led research programme: A descriptive analysis |
title_fullStr | Creating a database of internet-based clinical trials to support a public-led research programme: A descriptive analysis |
title_full_unstemmed | Creating a database of internet-based clinical trials to support a public-led research programme: A descriptive analysis |
title_short | Creating a database of internet-based clinical trials to support a public-led research programme: A descriptive analysis |
title_sort | creating a database of internet-based clinical trials to support a public-led research programme: a descriptive analysis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999056/ https://www.ncbi.nlm.nih.gov/pubmed/29942546 http://dx.doi.org/10.1177/2055207615617854 |
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