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Financial management of large, multi-center trials in a challenging funding milieu

BACKGROUND: Randomized clinical trials that have public health implications but no or low potential for commercial gain are predominantly funded by governmental (e.g., National Institutes of Health (NIH)) and not-for-profit organizations. Our objective was to develop an alternative clinical trial si...

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Autores principales: Lovegreen, Olivia, Riggs, Danielle, Staten, Myrlene A., Sheehan, Patricia, Pittas, Anastassios G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934907/
https://www.ncbi.nlm.nih.gov/pubmed/29724229
http://dx.doi.org/10.1186/s13063-018-2638-z
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author Lovegreen, Olivia
Riggs, Danielle
Staten, Myrlene A.
Sheehan, Patricia
Pittas, Anastassios G.
author_facet Lovegreen, Olivia
Riggs, Danielle
Staten, Myrlene A.
Sheehan, Patricia
Pittas, Anastassios G.
author_sort Lovegreen, Olivia
collection PubMed
description BACKGROUND: Randomized clinical trials that have public health implications but no or low potential for commercial gain are predominantly funded by governmental (e.g., National Institutes of Health (NIH)) and not-for-profit organizations. Our objective was to develop an alternative clinical trial site funding model for judicious allocation of declining public research funds. METHODS: In the Vitamin D and Type 2 Diabetes (D2d) study, an NIH-supported, large clinical trial testing the effect of vitamin D supplementation on incident diabetes in 2423 participants at high risk for diabetes, a hybrid financial management model for supporting collaborating clinical sites was developed and applied. The funding model employed two reimbursement components: Core (for study start-up and partial efforts throughout the study, ~40% of the total site budget), invoiced by sites, and Performance-Based Payments (for successful enrollment of participants and completion of follow-up visits, ~60% of the total site budget), automatically issued to the sites by the Coordinating Center based on actual recruitment and visits conducted. Underperforming sites transitioned to Performance-Based Payments only. RESULTS: Recruitment occurred from October 2013 through December 2016, requiring one additional year than the 2-year projection. Median enrollment at each site was 88 participants (range 29–318; 20 to 205% of the site target). At the end of year 1, study-wide recruitment was at 12% of the target (vs. 50% projected) and 12% of the total grant award was invested. The model constantly evaluated sites’ needs and re-allocated resources to meet the study enrollment goal. If D2d had issued cost reimbursement subaward agreements and sites invoiced for their entire budget, 83% of the award would have been spent for all study activities over the first 4 years of the trial compared to 65% of the award spent (US$26M) under the hybrid model used by D2d. CONCLUSIONS: It is feasible to foster a hybrid financial management approach to steward limited available public funds for research in a dynamic and consistent way that does not compromise the trial’s scientific integrity and ensures conservation of funds to complete recruitment and continue to follow up participants.
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spelling pubmed-59349072018-05-11 Financial management of large, multi-center trials in a challenging funding milieu Lovegreen, Olivia Riggs, Danielle Staten, Myrlene A. Sheehan, Patricia Pittas, Anastassios G. Trials Research BACKGROUND: Randomized clinical trials that have public health implications but no or low potential for commercial gain are predominantly funded by governmental (e.g., National Institutes of Health (NIH)) and not-for-profit organizations. Our objective was to develop an alternative clinical trial site funding model for judicious allocation of declining public research funds. METHODS: In the Vitamin D and Type 2 Diabetes (D2d) study, an NIH-supported, large clinical trial testing the effect of vitamin D supplementation on incident diabetes in 2423 participants at high risk for diabetes, a hybrid financial management model for supporting collaborating clinical sites was developed and applied. The funding model employed two reimbursement components: Core (for study start-up and partial efforts throughout the study, ~40% of the total site budget), invoiced by sites, and Performance-Based Payments (for successful enrollment of participants and completion of follow-up visits, ~60% of the total site budget), automatically issued to the sites by the Coordinating Center based on actual recruitment and visits conducted. Underperforming sites transitioned to Performance-Based Payments only. RESULTS: Recruitment occurred from October 2013 through December 2016, requiring one additional year than the 2-year projection. Median enrollment at each site was 88 participants (range 29–318; 20 to 205% of the site target). At the end of year 1, study-wide recruitment was at 12% of the target (vs. 50% projected) and 12% of the total grant award was invested. The model constantly evaluated sites’ needs and re-allocated resources to meet the study enrollment goal. If D2d had issued cost reimbursement subaward agreements and sites invoiced for their entire budget, 83% of the award would have been spent for all study activities over the first 4 years of the trial compared to 65% of the award spent (US$26M) under the hybrid model used by D2d. CONCLUSIONS: It is feasible to foster a hybrid financial management approach to steward limited available public funds for research in a dynamic and consistent way that does not compromise the trial’s scientific integrity and ensures conservation of funds to complete recruitment and continue to follow up participants. BioMed Central 2018-05-03 /pmc/articles/PMC5934907/ /pubmed/29724229 http://dx.doi.org/10.1186/s13063-018-2638-z Text en © The Author(s). 2018 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
Lovegreen, Olivia
Riggs, Danielle
Staten, Myrlene A.
Sheehan, Patricia
Pittas, Anastassios G.
Financial management of large, multi-center trials in a challenging funding milieu
title Financial management of large, multi-center trials in a challenging funding milieu
title_full Financial management of large, multi-center trials in a challenging funding milieu
title_fullStr Financial management of large, multi-center trials in a challenging funding milieu
title_full_unstemmed Financial management of large, multi-center trials in a challenging funding milieu
title_short Financial management of large, multi-center trials in a challenging funding milieu
title_sort financial management of large, multi-center trials in a challenging funding milieu
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934907/
https://www.ncbi.nlm.nih.gov/pubmed/29724229
http://dx.doi.org/10.1186/s13063-018-2638-z
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