Resource use and costs of investigator-sponsored randomized clinical trials in Switzerland, Germany, and the United Kingdom: a metaresearch study

Conducting high-quality randomized clinical trials (RCTs) is challenging and resource intensive. Funders and academic investigators depend on limited financial resources and, therefore, need empirical data for optimal budget planning. However, current literature lacks detailed empirical data on reso...

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Veröffentlicht in:Journal of clinical epidemiology 2024-12, Vol.176, p.111536, Article 111536
Hauptverfasser: Griessbach, Alexandra, Speich, Benjamin, Amstutz, Alain, Hausheer, Lena, Covino, Manuela, Wnfried Ramirez, Hillary, Schandelmaier, Stefan, Taji Heravi, Ala, Treweek, Shaun, Schwenkglenks, Matthias, Briel, Matthias, von Niederhäusern, Belinda, Hemkens, Lars G., Kasenda, Benjamin, Pauli-Magnus, Christiane, McLennan, Stuart
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container_title Journal of clinical epidemiology
container_volume 176
creator Griessbach, Alexandra
Speich, Benjamin
Amstutz, Alain
Hausheer, Lena
Covino, Manuela
Wnfried Ramirez, Hillary
Schandelmaier, Stefan
Taji Heravi, Ala
Treweek, Shaun
Schwenkglenks, Matthias
Briel, Matthias
Speich, Benjamin
von Niederhäusern, Belinda
Hemkens, Lars G.
Amstutz, Alain
Kasenda, Benjamin
Pauli-Magnus, Christiane
Schwenkglenks, Matthias
Briel, Matthias
Griessbach, Alexandra
McLennan, Stuart
Schandelmaier, Stefan
Taji Heravi, Ala
Treweek, Shaun
description Conducting high-quality randomized clinical trials (RCTs) is challenging and resource intensive. Funders and academic investigators depend on limited financial resources and, therefore, need empirical data for optimal budget planning. However, current literature lacks detailed empirical data on resource use and costs of investigator-sponsored RCTs. The aim of this study is to systematically collect cost data from investigator-sponsored RCTs from Switzerland, Germany, and the United Kingdom (UK). Principal investigators were asked to share their RCT cost and resource use data and enter it into an online case report form. We assessed cost patterns, cost drivers, and specific cost items, examined costs by study phase (planning-, conduct-, and finalization phase), compared planned with actual RCT costs, and explored differences in cost patterns across countries, medical fields, and intervention types. We included 93 RCTs which were initiated in Switzerland (n = 53; including eight conducted in low- and lower middle-income countries), Germany (n = 22), and the UK (n = 18). The median total trial cost in our RCT sample was $645,824 [interquartile range (IQR), $269,846–$1,577,924]. The median proportion of the total costs spent for planning phase was 27.5% [IQR, 20.6%–39.7%], for conduct phase 57.3% [IQR, 44.4%–66.3%], and for finalization phase 12.7% [IQR, 8.5%–19.3%] with little variation across countries. The items that contributed most to the total costs were protocol writing (7.2%; IQR 3.8%–10.6%), data management (5.0%; IQR 2.2%–8.1%) and follow-up (4.5%; IQR 2.3%–8.4%). Of the 66 RCTs with an available original budget, 46 (69.7%) exceeded the budget by over 50%. Use of routinely collected data to assess primary outcomes was independently associated with lower per patient- and lower total trial costs. Over a quarter of total trial costs were incurred in the planning phase, which is typically not fully funded. Two-thirds of RCTs exceeded their budget by more than 50%. Investigators and funders should consider empirical cost data to improve budgeting and funding practices. •Over a quarter (27.5%) of total trial costs were incurred in the trial planning phase.•Seventy percentage of RCTs exceeded their budget by more than 50%.•Key costs were protocol writing (7.2%), data management (5.0%), and follow-up (4.5%).•Factors associated with higher total cost included number of centers and longer duration.•Trials using routinely collected data for primary outcomes wer
doi_str_mv 10.1016/j.jclinepi.2024.111536
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Funders and academic investigators depend on limited financial resources and, therefore, need empirical data for optimal budget planning. However, current literature lacks detailed empirical data on resource use and costs of investigator-sponsored RCTs. The aim of this study is to systematically collect cost data from investigator-sponsored RCTs from Switzerland, Germany, and the United Kingdom (UK). Principal investigators were asked to share their RCT cost and resource use data and enter it into an online case report form. We assessed cost patterns, cost drivers, and specific cost items, examined costs by study phase (planning-, conduct-, and finalization phase), compared planned with actual RCT costs, and explored differences in cost patterns across countries, medical fields, and intervention types. We included 93 RCTs which were initiated in Switzerland (n = 53; including eight conducted in low- and lower middle-income countries), Germany (n = 22), and the UK (n = 18). The median total trial cost in our RCT sample was $645,824 [interquartile range (IQR), $269,846–$1,577,924]. The median proportion of the total costs spent for planning phase was 27.5% [IQR, 20.6%–39.7%], for conduct phase 57.3% [IQR, 44.4%–66.3%], and for finalization phase 12.7% [IQR, 8.5%–19.3%] with little variation across countries. The items that contributed most to the total costs were protocol writing (7.2%; IQR 3.8%–10.6%), data management (5.0%; IQR 2.2%–8.1%) and follow-up (4.5%; IQR 2.3%–8.4%). Of the 66 RCTs with an available original budget, 46 (69.7%) exceeded the budget by over 50%. Use of routinely collected data to assess primary outcomes was independently associated with lower per patient- and lower total trial costs. Over a quarter of total trial costs were incurred in the planning phase, which is typically not fully funded. Two-thirds of RCTs exceeded their budget by more than 50%. Investigators and funders should consider empirical cost data to improve budgeting and funding practices. •Over a quarter (27.5%) of total trial costs were incurred in the trial planning phase.•Seventy percentage of RCTs exceeded their budget by more than 50%.•Key costs were protocol writing (7.2%), data management (5.0%), and follow-up (4.5%).•Factors associated with higher total cost included number of centers and longer duration.•Trials using routinely collected data for primary outcomes were associated with lower costs.</description><identifier>ISSN: 0895-4356</identifier><identifier>ISSN: 1878-5921</identifier><identifier>EISSN: 1878-5921</identifier><identifier>DOI: 10.1016/j.jclinepi.2024.111536</identifier><identifier>PMID: 39307405</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Budget ; Budgets ; Clinical trials ; Costs ; Costs and Cost Analysis ; Data collection ; Data management ; Funding ; Germany ; Health Resources - economics ; Health Resources - statistics &amp; numerical data ; Humans ; Medical research ; Oncology ; Randomized controlled trials ; Randomized Controlled Trials as Topic - economics ; Randomized Controlled Trials as Topic - statistics &amp; numerical data ; Regression analysis ; Research Personnel - economics ; Research Personnel - statistics &amp; numerical data ; Resource-use ; Switzerland ; United Kingdom ; Variables</subject><ispartof>Journal of clinical epidemiology, 2024-12, Vol.176, p.111536, Article 111536</ispartof><rights>2024 The Authors</rights><rights>Copyright © 2024 The Authors. 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The median total trial cost in our RCT sample was $645,824 [interquartile range (IQR), $269,846–$1,577,924]. The median proportion of the total costs spent for planning phase was 27.5% [IQR, 20.6%–39.7%], for conduct phase 57.3% [IQR, 44.4%–66.3%], and for finalization phase 12.7% [IQR, 8.5%–19.3%] with little variation across countries. The items that contributed most to the total costs were protocol writing (7.2%; IQR 3.8%–10.6%), data management (5.0%; IQR 2.2%–8.1%) and follow-up (4.5%; IQR 2.3%–8.4%). Of the 66 RCTs with an available original budget, 46 (69.7%) exceeded the budget by over 50%. Use of routinely collected data to assess primary outcomes was independently associated with lower per patient- and lower total trial costs. Over a quarter of total trial costs were incurred in the planning phase, which is typically not fully funded. Two-thirds of RCTs exceeded their budget by more than 50%. 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Calcified Tissue Abstracts</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical epidemiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Griessbach, Alexandra</au><au>Speich, Benjamin</au><au>Amstutz, Alain</au><au>Hausheer, Lena</au><au>Covino, Manuela</au><au>Wnfried Ramirez, Hillary</au><au>Schandelmaier, Stefan</au><au>Taji Heravi, Ala</au><au>Treweek, Shaun</au><au>Schwenkglenks, Matthias</au><au>Briel, Matthias</au><au>Speich, Benjamin</au><au>von Niederhäusern, Belinda</au><au>Hemkens, Lars G.</au><au>Amstutz, Alain</au><au>Kasenda, Benjamin</au><au>Pauli-Magnus, Christiane</au><au>Schwenkglenks, Matthias</au><au>Briel, Matthias</au><au>Griessbach, Alexandra</au><au>McLennan, Stuart</au><au>Schandelmaier, Stefan</au><au>Taji Heravi, Ala</au><au>Treweek, Shaun</au><aucorp>MAking Randomized Trials Affordable (MARTA) Group</aucorp><aucorp>MAking Randomized Trials Affordable (MARTA) Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Resource use and costs of investigator-sponsored randomized clinical trials in Switzerland, Germany, and the United Kingdom: a metaresearch study</atitle><jtitle>Journal of clinical epidemiology</jtitle><addtitle>J Clin Epidemiol</addtitle><date>2024-12</date><risdate>2024</risdate><volume>176</volume><spage>111536</spage><pages>111536-</pages><artnum>111536</artnum><issn>0895-4356</issn><issn>1878-5921</issn><eissn>1878-5921</eissn><abstract>Conducting high-quality randomized clinical trials (RCTs) is challenging and resource intensive. Funders and academic investigators depend on limited financial resources and, therefore, need empirical data for optimal budget planning. However, current literature lacks detailed empirical data on resource use and costs of investigator-sponsored RCTs. The aim of this study is to systematically collect cost data from investigator-sponsored RCTs from Switzerland, Germany, and the United Kingdom (UK). Principal investigators were asked to share their RCT cost and resource use data and enter it into an online case report form. We assessed cost patterns, cost drivers, and specific cost items, examined costs by study phase (planning-, conduct-, and finalization phase), compared planned with actual RCT costs, and explored differences in cost patterns across countries, medical fields, and intervention types. We included 93 RCTs which were initiated in Switzerland (n = 53; including eight conducted in low- and lower middle-income countries), Germany (n = 22), and the UK (n = 18). The median total trial cost in our RCT sample was $645,824 [interquartile range (IQR), $269,846–$1,577,924]. The median proportion of the total costs spent for planning phase was 27.5% [IQR, 20.6%–39.7%], for conduct phase 57.3% [IQR, 44.4%–66.3%], and for finalization phase 12.7% [IQR, 8.5%–19.3%] with little variation across countries. The items that contributed most to the total costs were protocol writing (7.2%; IQR 3.8%–10.6%), data management (5.0%; IQR 2.2%–8.1%) and follow-up (4.5%; IQR 2.3%–8.4%). Of the 66 RCTs with an available original budget, 46 (69.7%) exceeded the budget by over 50%. Use of routinely collected data to assess primary outcomes was independently associated with lower per patient- and lower total trial costs. Over a quarter of total trial costs were incurred in the planning phase, which is typically not fully funded. Two-thirds of RCTs exceeded their budget by more than 50%. Investigators and funders should consider empirical cost data to improve budgeting and funding practices. •Over a quarter (27.5%) of total trial costs were incurred in the trial planning phase.•Seventy percentage of RCTs exceeded their budget by more than 50%.•Key costs were protocol writing (7.2%), data management (5.0%), and follow-up (4.5%).•Factors associated with higher total cost included number of centers and longer duration.•Trials using routinely collected data for primary outcomes were associated with lower costs.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>39307405</pmid><doi>10.1016/j.jclinepi.2024.111536</doi><orcidid>https://orcid.org/0000-0002-2070-5230</orcidid><orcidid>https://orcid.org/0000-0002-3301-8085</orcidid><orcidid>https://orcid.org/0000-0003-1716-993X</orcidid><orcidid>https://orcid.org/0000-0002-8429-0337</orcidid><orcidid>https://orcid.org/0000-0003-3726-1856</orcidid><orcidid>https://orcid.org/0000-0003-3752-1611</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0895-4356
ispartof Journal of clinical epidemiology, 2024-12, Vol.176, p.111536, Article 111536
issn 0895-4356
1878-5921
1878-5921
language eng
recordid cdi_pubmed_primary_39307405
source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Budget
Budgets
Clinical trials
Costs
Costs and Cost Analysis
Data collection
Data management
Funding
Germany
Health Resources - economics
Health Resources - statistics & numerical data
Humans
Medical research
Oncology
Randomized controlled trials
Randomized Controlled Trials as Topic - economics
Randomized Controlled Trials as Topic - statistics & numerical data
Regression analysis
Research Personnel - economics
Research Personnel - statistics & numerical data
Resource-use
Switzerland
United Kingdom
Variables
title Resource use and costs of investigator-sponsored randomized clinical trials in Switzerland, Germany, and the United Kingdom: a metaresearch study
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