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Continued investigator engagement: Reasons principal investigators conduct multiple FDA-regulated drug trials

BACKGROUND/AIMS: Numerous reasons have been identified for why U.S.-based principal investigators choose to not continue participating in FDA-regulated trials. However, unexplored are reasons why a substantial number of principal investigators, facing the same challenges, remain engaged in clinical...

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Autores principales: Dombeck, Carrie B., Hinkley, Terri, Fordyce, Christopher B., Blanchard, Katelyn, Roe, Matthew T., Corneli, Amy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6926102/
https://www.ncbi.nlm.nih.gov/pubmed/31890985
http://dx.doi.org/10.1016/j.conctc.2019.100502
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author Dombeck, Carrie B.
Hinkley, Terri
Fordyce, Christopher B.
Blanchard, Katelyn
Roe, Matthew T.
Corneli, Amy
author_facet Dombeck, Carrie B.
Hinkley, Terri
Fordyce, Christopher B.
Blanchard, Katelyn
Roe, Matthew T.
Corneli, Amy
author_sort Dombeck, Carrie B.
collection PubMed
description BACKGROUND/AIMS: Numerous reasons have been identified for why U.S.-based principal investigators choose to not continue participating in FDA-regulated trials. However, unexplored are reasons why a substantial number of principal investigators, facing the same challenges, remain engaged in clinical research. This study aimed to both describe barriers and identify factors that contribute to active investigators’ success in conducting multiple FDA-regulated trials. METHODS: We conducted qualitative in-depth interviews (IDIs) with “active” multi-trial investigators. Interviews focused on investigators’ experiences with FDA-regulated drug trials, challenges faced, and factors contributing to success. Investigators also reflected on previously identified barriers and shared advice for new investigators. Narratives were analyzed using applied thematic analysis. RESULTS: We interviewed 23 experienced investigators, representing a variety of backgrounds. Most reported that demonstrated ability to conduct a trial led to being approached again by sponsors. Investigators cited infrastructure, staff support, advance planning, and personal qualities as key factors in successfully conducting multiple trials. Nearly all cited difficulties related to trial finances. Three-quarters pointed to challenges with patient recruitment; others described challenges related to data and safety reporting and to the time that trial implementation takes away from other activities. Aspiring investigators were advised to engage in research-specific training and seek out mentorship opportunities. CONCLUSION: Investigators in our sample faced many of the same challenges identified in previous research, yet they had evolved strategies to overcome them. The amount and type of support to which investigators have access may represent a crucial difference between “active” investigators and principal investigators who leave FDA-regulated trials.
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spelling pubmed-69261022019-12-30 Continued investigator engagement: Reasons principal investigators conduct multiple FDA-regulated drug trials Dombeck, Carrie B. Hinkley, Terri Fordyce, Christopher B. Blanchard, Katelyn Roe, Matthew T. Corneli, Amy Contemp Clin Trials Commun Article BACKGROUND/AIMS: Numerous reasons have been identified for why U.S.-based principal investigators choose to not continue participating in FDA-regulated trials. However, unexplored are reasons why a substantial number of principal investigators, facing the same challenges, remain engaged in clinical research. This study aimed to both describe barriers and identify factors that contribute to active investigators’ success in conducting multiple FDA-regulated trials. METHODS: We conducted qualitative in-depth interviews (IDIs) with “active” multi-trial investigators. Interviews focused on investigators’ experiences with FDA-regulated drug trials, challenges faced, and factors contributing to success. Investigators also reflected on previously identified barriers and shared advice for new investigators. Narratives were analyzed using applied thematic analysis. RESULTS: We interviewed 23 experienced investigators, representing a variety of backgrounds. Most reported that demonstrated ability to conduct a trial led to being approached again by sponsors. Investigators cited infrastructure, staff support, advance planning, and personal qualities as key factors in successfully conducting multiple trials. Nearly all cited difficulties related to trial finances. Three-quarters pointed to challenges with patient recruitment; others described challenges related to data and safety reporting and to the time that trial implementation takes away from other activities. Aspiring investigators were advised to engage in research-specific training and seek out mentorship opportunities. CONCLUSION: Investigators in our sample faced many of the same challenges identified in previous research, yet they had evolved strategies to overcome them. The amount and type of support to which investigators have access may represent a crucial difference between “active” investigators and principal investigators who leave FDA-regulated trials. Elsevier 2019-11-23 /pmc/articles/PMC6926102/ /pubmed/31890985 http://dx.doi.org/10.1016/j.conctc.2019.100502 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dombeck, Carrie B.
Hinkley, Terri
Fordyce, Christopher B.
Blanchard, Katelyn
Roe, Matthew T.
Corneli, Amy
Continued investigator engagement: Reasons principal investigators conduct multiple FDA-regulated drug trials
title Continued investigator engagement: Reasons principal investigators conduct multiple FDA-regulated drug trials
title_full Continued investigator engagement: Reasons principal investigators conduct multiple FDA-regulated drug trials
title_fullStr Continued investigator engagement: Reasons principal investigators conduct multiple FDA-regulated drug trials
title_full_unstemmed Continued investigator engagement: Reasons principal investigators conduct multiple FDA-regulated drug trials
title_short Continued investigator engagement: Reasons principal investigators conduct multiple FDA-regulated drug trials
title_sort continued investigator engagement: reasons principal investigators conduct multiple fda-regulated drug trials
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6926102/
https://www.ncbi.nlm.nih.gov/pubmed/31890985
http://dx.doi.org/10.1016/j.conctc.2019.100502
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