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Adapting to the COVID-19 pandemic on Building Research in Diet and Cognition (BRIDGE) trial
BACKGROUND: The COVID-19 pandemic has altered the research landscape for clinical trials, requiring thoughtful consideration regarding how to handle the risks and benefits of continuing them. DESIGN: This brief report describes the experience of adapting the Building Research in Diet and Cognition (...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8284687/ https://www.ncbi.nlm.nih.gov/pubmed/34271944 http://dx.doi.org/10.1186/s13063-021-05383-6 |
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author | Fitzgibbon, Marian Blumstein, Lara Schiffer, Linda Antonic, Mirjana A. McLeod, Andrew Dakers, Roxanne Restrepo, Leo Boots, Elizabeth A. Sanchez-Flack, Jennifer C. Tussing-Humphreys, Lisa Lamar, Melissa |
author_facet | Fitzgibbon, Marian Blumstein, Lara Schiffer, Linda Antonic, Mirjana A. McLeod, Andrew Dakers, Roxanne Restrepo, Leo Boots, Elizabeth A. Sanchez-Flack, Jennifer C. Tussing-Humphreys, Lisa Lamar, Melissa |
author_sort | Fitzgibbon, Marian |
collection | PubMed |
description | BACKGROUND: The COVID-19 pandemic has altered the research landscape for clinical trials, requiring thoughtful consideration regarding how to handle the risks and benefits of continuing them. DESIGN: This brief report describes the experience of adapting the Building Research in Diet and Cognition (BRIDGE) study, a randomized clinical trial examining the effects of the Mediterranean diet, with and without weight loss, on cognitive functioning in 185 older obese African American adults during the COVID-19 pandemic. MEASUREMENT: The University of Illinois at Chicago (UIC) developed an expedited amendment process for research shifting to remote data collection. We conducted the study in three consecutive groups. For group 3, 14-month data collection period, we adapted our protocol to allow data collection via telephone and e-mail. We were unable to collect certain measures that required face-to-face contact. RESULTS: For measures that could be collected remotely, 14-month retention was similar for group 3 compared to groups 1 and 2: data were collected for 86.9% of group 3 (remote) and 87.9% of groups 1 and 2 (face to face), p = .84. CONCLUSIONS: In order to preserve the integrity of our clinical trial and ensure the safety of our participants and staff during the COVID-19 pandemic, we had to carefully and efficiently adapt our data collection procedures. The procedures put in place allowed us to collect our primary outcomes and the majority of our secondary outcomes and will enable us to examine the role of dietary intake, with and without weight loss, on cognitive functioning in a vulnerable and high-risk population. TRIAL REGISTRATION: ClinicalTrials.gov NCT3129048. Registration Date: 4/17/2017. |
format | Online Article Text |
id | pubmed-8284687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82846872021-07-19 Adapting to the COVID-19 pandemic on Building Research in Diet and Cognition (BRIDGE) trial Fitzgibbon, Marian Blumstein, Lara Schiffer, Linda Antonic, Mirjana A. McLeod, Andrew Dakers, Roxanne Restrepo, Leo Boots, Elizabeth A. Sanchez-Flack, Jennifer C. Tussing-Humphreys, Lisa Lamar, Melissa Trials Commentary BACKGROUND: The COVID-19 pandemic has altered the research landscape for clinical trials, requiring thoughtful consideration regarding how to handle the risks and benefits of continuing them. DESIGN: This brief report describes the experience of adapting the Building Research in Diet and Cognition (BRIDGE) study, a randomized clinical trial examining the effects of the Mediterranean diet, with and without weight loss, on cognitive functioning in 185 older obese African American adults during the COVID-19 pandemic. MEASUREMENT: The University of Illinois at Chicago (UIC) developed an expedited amendment process for research shifting to remote data collection. We conducted the study in three consecutive groups. For group 3, 14-month data collection period, we adapted our protocol to allow data collection via telephone and e-mail. We were unable to collect certain measures that required face-to-face contact. RESULTS: For measures that could be collected remotely, 14-month retention was similar for group 3 compared to groups 1 and 2: data were collected for 86.9% of group 3 (remote) and 87.9% of groups 1 and 2 (face to face), p = .84. CONCLUSIONS: In order to preserve the integrity of our clinical trial and ensure the safety of our participants and staff during the COVID-19 pandemic, we had to carefully and efficiently adapt our data collection procedures. The procedures put in place allowed us to collect our primary outcomes and the majority of our secondary outcomes and will enable us to examine the role of dietary intake, with and without weight loss, on cognitive functioning in a vulnerable and high-risk population. TRIAL REGISTRATION: ClinicalTrials.gov NCT3129048. Registration Date: 4/17/2017. BioMed Central 2021-07-16 /pmc/articles/PMC8284687/ /pubmed/34271944 http://dx.doi.org/10.1186/s13063-021-05383-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 | Commentary Fitzgibbon, Marian Blumstein, Lara Schiffer, Linda Antonic, Mirjana A. McLeod, Andrew Dakers, Roxanne Restrepo, Leo Boots, Elizabeth A. Sanchez-Flack, Jennifer C. Tussing-Humphreys, Lisa Lamar, Melissa Adapting to the COVID-19 pandemic on Building Research in Diet and Cognition (BRIDGE) trial |
title | Adapting to the COVID-19 pandemic on Building Research in Diet and Cognition (BRIDGE) trial |
title_full | Adapting to the COVID-19 pandemic on Building Research in Diet and Cognition (BRIDGE) trial |
title_fullStr | Adapting to the COVID-19 pandemic on Building Research in Diet and Cognition (BRIDGE) trial |
title_full_unstemmed | Adapting to the COVID-19 pandemic on Building Research in Diet and Cognition (BRIDGE) trial |
title_short | Adapting to the COVID-19 pandemic on Building Research in Diet and Cognition (BRIDGE) trial |
title_sort | adapting to the covid-19 pandemic on building research in diet and cognition (bridge) trial |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8284687/ https://www.ncbi.nlm.nih.gov/pubmed/34271944 http://dx.doi.org/10.1186/s13063-021-05383-6 |
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