Evidence map›Paper›PMID 34102012›Full record

Trial reportCancer medicine2021

Randomized study of remote telehealth genetic services versus usual care in oncology practices without genetic counselors.

Cara N Cacioppo, Brian L Egleston, Dominique Fetzer, Colleen Burke Sands, Syeda A Raza, Neeraja Reddy Malleda, Elisabeth McCarty Wood, India Rittenburg, Julianne Childs, David Cho and 10 more

Open access · goldAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Cancer medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
3.1field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 29 citations in OpenAlex.

  1. Pooled it
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  6. Mainstreaming genetic testing in community oncology settings.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
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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

20 authors at 9 institutions in 1 country.

Cara N CacioppoPenn Telegenetics Program, University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0003-4761-7027
Brian L EglestonFox Chase Cancer Center, Biostatistics and Bioinformatics Facility, Temple University Health System, Philadelphia, PA, USA.ORCID 0000-0002-1633-799X
Dominique FetzerDepartment of Medicine, Division of Hematology-Oncology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Colleen Burke SandsDepartment of Medicine, Division of Hematology-Oncology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Syeda A RazaDepartment of Medicine, Division of Hematology-Oncology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Neeraja Reddy MalledaPenn Telegenetics Program, University of Pennsylvania, Philadelphia, PA, USA.
Elisabeth McCarty WoodPenn Telegenetics Program, University of Pennsylvania, Philadelphia, PA, USA.
India RittenburgPenn Telegenetics Program, University of Pennsylvania, Philadelphia, PA, USA.
Julianne ChildsShore Cancer Center, Somers Point, NJ, USA.
David ChoCape Regional Medical Center, Cape May Court House, NJ, USA.
Martha HosfordUnion Hospital, Elkton, MD, USA.
Tina KhairGettysburg Cancer Center, Gettysburg, PA, USA.
Jamil KhatriUnion Hospital, Elkton, MD, USA.
Lydia KomarnickyDrexel University Cancer Center, Philadelphia, PA, USA.
Trina PorettaKennedy Cancer Center, Sewell, NJ, USA.
Fahd RahmanUnion Hospital, Elkton, MD, USA.
Satish ShahGettysburg Cancer Center, Gettysburg, PA, USA.
Linda J Patrick-MillerCenter for Clinical Cancer Genetics and Global Health, The University of Chicago, Chicago, IL, USA.
Susan M DomchekDepartment of Medicine, Division of Hematology-Oncology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Angela R BradburyPenn Telegenetics Program, University of Pennsylvania, Philadelphia, PA, USA.
Penn Center for AIDS Research · USUniversity of Pennsylvania · USUnion Hospital · USGettysburg College · USDrexel University · USFox Chase Cancer Center · USRegional Medical Center · USShore Memorial Hospital · USUniversity of Chicago · US

Funding

Basser Center
6 · The paper itself

Abstract

purposeTo examine the benefit of telehealth over current delivery options in oncology practices without genetic counselors.

methodsParticipants meeting cancer genetic testing guidelines were recruited to this multi-center, randomized trial comparing uptake of genetic services with remote services (telephone or videoconference) to usual care in six predominantly community practices without genetic counselors. The primary outcome was the composite uptake of genetic counseling or testing. Secondary outcomes compare telephone versus videoconference services.

results147 participants enrolled and 119 were randomized. Eighty percent of participants in the telehealth arm had genetic services as compared to 16% in the usual care arm (OR 30.52, p < 0.001). Five genetic mutation carriers (6.7%) were identified in the telehealth arm, compared to none in the usual care arm. In secondary analyses, factors associated with uptake were lower anxiety (6.77 vs. 8.07, p = 0.04) and lower depression (3.38 vs. 5.06, p = 0.04) among those who had genetic services. There were no significant differences in change in cognitive or affective outcomes immediately post-counseling and at 6 and 12 months between telephone and videoconference arms.

conclusionTelehealth increases uptake of genetic counseling and testing at oncology practices without genetic counselors and could significantly improve identification of genetic carriers and cancer prevention outcomes.

Indexed as

AnxietyCounselorsDepressionFemaleGenetic Carrier ScreeningGenetic CounselingGenetic ServicesGenetic TestingHumansMaleMedical OncologyMiddle AgedMutation RateSocioeconomic FactorsTelemedicineTelephonealternative service deliverycancer geneticscancer predisposition syndromesgenetic counselinggeneticsgenetic testingtelegeneticstelehealthtelemedicine

Identifiers

PMID34102012
PMCPMC8267134
OpenAlexW3170633474

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.