Evidence map›Paper›PMID 37588676›Full record

ArticleJournal of clinical and translational science2023

Preparing clinicians to be site investigators in multicenter clinical trials: A training program at an academic medical center.

Tammy L Loucks, Diana Lee-Chavarria, Jillian Harvey, Rechelle Paranal, Signe Denmark, Patrick A Flume, Marc Chimowitz, Tanya N Turan

Abstract read
In one paragraph

Article in Journal of clinical and translational science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Trial
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Tammy L LoucksSouth Carolina Clinical and Translational Research Institute, Medical University of South Carolina, Charleston, SC, USA.ORCID https://orcid.org/0000-0001-7651-7602
Diana Lee-ChavarriaSouth Carolina Clinical and Translational Research Institute, Medical University of South Carolina, Charleston, SC, USA.
Jillian HarveySouth Carolina Clinical and Translational Research Institute, Medical University of South Carolina, Charleston, SC, USA.ORCID https://orcid.org/0000-0002-6814-8226
Rechelle ParanalSouth Carolina Clinical and Translational Research Institute, Medical University of South Carolina, Charleston, SC, USA.
Signe DenmarkSouth Carolina Clinical and Translational Research Institute, Medical University of South Carolina, Charleston, SC, USA.
Patrick A FlumeSouth Carolina Clinical and Translational Research Institute, Medical University of South Carolina, Charleston, SC, USA.
Marc ChimowitzSouth Carolina Clinical and Translational Research Institute, Medical University of South Carolina, Charleston, SC, USA.
Tanya N TuranSouth Carolina Clinical and Translational Research Institute, Medical University of South Carolina, Charleston, SC, USA.

Funding

South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
NCATS NIH HHS UL1 TR001450
6 · The paper itself

Abstract

Clinical trials are essential in the translation of biomedical discoveries to new clinical interventions and therapeutics. Successful multisite clinical trials require qualified site investigators with an understanding of the full spectrum of processes and requirements from trial identification through closeout. New site investigators may be deterred by competing demands on their time, the complexity of administrative and regulatory processes for trial initiation and conduct, and limited access to experienced mentor networks. We established a Clinical Trialist Training Program (CTTP) and complimentary Clinical Trials Bootcamp at our institution to address these barriers and increase the number of local site investigators enabled to lead successful clinical trials. An initial cohort of four CTTP scholars received salary support with protected time, didactic training, assistance with study identification and start-up navigation, and quarterly progress meetings. By the end of the 12-month program, this initial cohort identified 33 new trials, utilized feasibility assessments, and reported being on target to sustain their protected time from new clinical trials. Bootcamp attendees demonstrated increased knowledge of resources, offices, and processes associated with clinical trial conduct. Our results support providing compensated protected time, training, and access to experienced clinical research professionals to enable clinicians to become successful site investigators.

Indexed as

capacity buildingclinical trialEducationprogramresearch personnel

Identifiers

PMID37588676
PMCPMC10425868

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.