Evidence map›Paper›PMID 36999823›Full record

ArticleTranslational behavioral medicine2023

Rapid-cycle designs to adapt interventions for COVID-19 in safety-net healthcare systems.

Chelsey R Schlechter, Thomas J Reese, Jennifer Wirth, Bryan Gibson, Kensaku Kawamoto, Tracey Siaperas, Alan Pruhs, Courtney Pariera Dinkins, Yue Zhang, Michael Friedrichs and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in Translational behavioral medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.9field-weighted citation impact, top 7% of its field
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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. 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

22 authors at 4 institutions in 1 country.

Chelsey R SchlechterDepartment of Population Health Sciences, University of Utah, Salt Lake City, UT, USA.
Thomas J ReeseDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, USA.
Jennifer WirthHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Bryan GibsonDepartment of Biomedical Informatics, University of Utah, Salt Lake City, UT, USA.
Kensaku KawamotoDepartment of Biomedical Informatics, University of Utah, Salt Lake City, UT, USA.ORCID 0000-0003-4282-9338
Tracey SiaperasAssociation for Utah Community Health, Salt Lake City, UT, USA.
Alan PruhsAssociation for Utah Community Health, Salt Lake City, UT, USA.
Courtney Pariera DinkinsAssociation for Utah Community Health, Salt Lake City, UT, USA.
Yue ZhangDepartment of Population Health Sciences, University of Utah, Salt Lake City, UT, USA.
Michael FriedrichsUtah Department of Health and Human Services, Salt Lake City, UT, USA.
Stephanie GeorgeUtah Department of Health and Human Services, Salt Lake City, UT, USA.
Cho Y LamDepartment of Population Health Sciences, University of Utah, Salt Lake City, UT, USA.
Joni H PierceDepartment of Biomedical Informatics, University of Utah, Salt Lake City, UT, USA.
Emerson P BorsatoDepartment of Biomedical Informatics, University of Utah, Salt Lake City, UT, USA.
Ryan C CorniaDepartment of Biomedical Informatics, University of Utah, Salt Lake City, UT, USA.
Leticia StevensDepartment of Biomedical Informatics, University of Utah, Salt Lake City, UT, USA.
Anna MartinezHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Richard L BradshawDepartment of Biomedical Informatics, University of Utah, Salt Lake City, UT, USA.
Kimberly A KaphingstHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Rachel HessDepartment of Population Health Sciences, University of Utah, Salt Lake City, UT, USA.
Guilherme Del FiolDepartment of Biomedical Informatics, University of Utah, Salt Lake City, UT, USA.ORCID 0000-0001-9954-6799
David W WetterDepartment of Population Health Sciences, University of Utah, Salt Lake City, UT, USA.
University of Utah · USAssociation for Utah Community Health · USUtah Department of Health · USVanderbilt University Medical Center · US

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jared P Rutter · 1986 to 2026
$72.6M
Utah Center for Clinical and Translational ScienceUL1TR002538 · NCATS · UNIVERSITY OF UTAH · PI HESS, RACHEL, MAJERSIK, JENNIFER JUHL · 2018 to 2022
$26.0M
CTSA UM1 Program at University of UtahUM1TR004409 · NCATS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI RACHEL HESS, Jennifer Juhl Majersik · 2023 to 2026
$21.9M
NCATS NIH HHS UL1 TR002538NCATS NIH HHS UM1 TR004409NCI NIH HHS P30 CA042014NCI NIH HHS P30CA042014NIH HHS UL1TR002538
6 · The paper itself

Abstract

Racial/ethnic minority, low socioeconomic status, and rural populations are disproportionately affected by COVID-19. Developing and evaluating interventions to address COVID-19 testing and vaccination among these populations are crucial to improving health inequities. The purpose of this paper is to describe the application of a rapid-cycle design and adaptation process from an ongoing trial to address COVID-19 among safety-net healthcare system patients. The rapid-cycle design and adaptation process included: (a) assessing context and determining relevant models/frameworks; (b) determining core and modifiable components of interventions; and (c) conducting iterative adaptations using Plan-Do-Study-Act (PDSA) cycles. PDSA cycles included: Plan. Gather information from potential adopters/implementers (e.g., Community Health Center [CHC] staff/patients) and design initial interventions; Do. Implement interventions in single CHC or patient cohort; Study. Examine process, outcome, and context data (e.g., infection rates); and, Act. If necessary, refine interventions based on process and outcome data, then disseminate interventions to other CHCs and patient cohorts. Seven CHC systems with 26 clinics participated in the trial. Rapid-cycle, PDSA-based adaptations were made to adapt to evolving COVID-19-related needs. Near real-time data used for adaptation included data on infection hot spots, CHC capacity, stakeholder priorities, local/national policies, and testing/vaccine availability. Adaptations included those to study design, intervention content, and intervention cohorts. Decision-making included multiple stakeholders (e.g., State Department of Health, Primary Care Association, CHCs, patients, researchers). Rapid-cycle designs may improve the relevance and timeliness of interventions for CHCs and other settings that provide care to populations experiencing health inequities, and for rapidly evolving healthcare challenges such as COVID-19.

Indexed as

COVID-19EthnicityCOVID-19 TestingDelivery of Health CareHumansMinority GroupsAdaptationCOVID-19Health equityRapid-cycle designsSafety-net healthcare systems

Identifiers

PMID36999823
PMCPMC10255772
OpenAlexW4362458805

What OpenQuestion holds

Textmetadata
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.