Evidence map›Paper›PMID 38803214›Full record

ArticleJournal of genetic counseling2025

Impact of barriers and motivators on intention and confidence to undergo hereditary cancer genetic testing.

Sarah Austin, Erika N Hanson, Emerson Delacroix, Elizabeth Bacon, John Rice, Lynette Hammond Gerido, Elizabeth Rizzo, Versha Pleasant, Elena M Stoffel, Jennifer J Griggs and 1 more

Abstract read
In one paragraph

Article in Journal of genetic counseling, 2025. 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
–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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Uptake of Polygenic Risk Testing for Glaucoma in Unaffected Individuals.Translational vision science & technology · 2026
    Article
  5. Article
  6. Article
  7. Article
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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

11 authors.

Sarah AustinRogel Cancer Center, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0003-4484-9746
Erika N HansonDepartment of Internal Medicine, University of Michigan School of Medicine, Ann Arbor, Michigan, USA.ORCID 0000-0002-5952-0962
Emerson DelacroixRogel Cancer Center, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0003-1045-7963
Elizabeth BaconDepartment of Internal Medicine, University of Michigan School of Medicine, Ann Arbor, Michigan, USA.
John RiceUniversity of Michigan School of Public Health, Ann Arbor, Michigan, USA.
Lynette Hammond GeridoCase Western Reserve University School of Medicine, Cleveland, Ohio, USA.
Elizabeth RizzoDepartment of Internal Medicine, University of Michigan School of Medicine, Ann Arbor, Michigan, USA.
Versha PleasantRogel Cancer Center, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0003-2752-9636
Elena M StoffelRogel Cancer Center, University of Michigan, Ann Arbor, Michigan, USA.
Jennifer J GriggsRogel Cancer Center, University of Michigan, Ann Arbor, Michigan, USA.
Ken ResnicowRogel Cancer Center, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0003-1416-9627

Funding

Innovative Approaches to Expand Cancer Genetic Screening and Testing for Patients & Families in a Statewide Oncology Network through Community, State, & Payer PartnershipsU01CA232827 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GRIGGS, JENNIFER J, RESNICOW, KEN A. · 2020 to 2020
$4.0M
FITting noninvasive testing into Lynch syndrome colorectal cancer surveillance: a multicenter, prospective trialR01CA287257 · NCI · UNIVERSITY OF CHICAGO · PI Fay Kastrinos, Sonia Kupfer · 2024 to 2026
$3.4M
University of Michigan Training Program in ELSI ResearchT32HG010030 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ROBERTS, SCOTT · 2018 to 2022
$962k
NCI NIH HHS L60 CA274876NCI NIH HHS R01 CA287257NCI NIH HHS U01 CA232827NCI NIH HHS U01 CA232827-05NHGRI NIH HHS T32 HG010030
6 · The paper itself

Abstract

Genetic testing for hereditary cancer syndromes can provide lifesaving information allowing for individualized cancer screening, prevention, and treatment. However, the determinants, both barriers and motivators, of genetic testing intention are not well described. A survey of barriers and motivators to genetic testing was emailed to adult patients eligible for genetic testing based on cancer diagnosis who previously have not had genetic testing (n = 201). Associations between barriers/motivators with testing intention and confidence were examined first by correlation followed by multivariable linear regression model holding constant potential covariates. Seven barrier items from two domains (logistics and genetic testing knowledge) were found to significantly negatively correlate with genetic testing intention. Unexpectedly, three barrier items had significant positive correlation with genetic testing intention; these were related to family worry (passing a condition on to future generations) and testing knowledge (needing more information on the genetic testing process and what it has to offer). Ten barrier items had significant negative correlation with confidence to get a genetic test and encompassed four domains: stigma, insurance/genetic discrimination, knowledge, and cost. All motivator items were associated with intention to get a genetic test, while none were associated with confidence. Multivariable analysis yielded six total barriers (five from the knowledge domain, one from cost domain) and two motivators (relieved to know and treatment impact) that were significantly associated with genetic testing intention or confidence when controlling for demographic characteristics. These findings indicate the need for tailored interventions to amplify motivating factors and counter-message barriers to enhance patient motivation and confidence to undergo testing.

Indexed as

Genetic TestingIntentionMotivationNeoplasmsAdultFemaleHumansMaleMiddle AgedSurveys and Questionnairesbarriersgenetic testinghealth behaviorintentionknowledge

Identifiers

PMID38803214
PMCPMC11599461

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.