Evidence map›Paper›PMID 32242760›Full record

Trial reportJournal of empirical research on human research ethics : JERHRE2020

Comparison of Video, App, and Standard Consent Processes on Decision-Making for Biospecimen Research: A Randomized Controlled Trial.

Erin Rothwell, Erin Johnson, Bob Wong, Aaron Goldenberg, Beth A Tarini, Naomi Riches, Louisa A Stark, Christina Pries, Carrie Langbo, Elizabeth Langen and 1 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of empirical research on human research ethics : JERHRE, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Comparative Effectiveness of eConsent: Systematic Review.Journal of medical Internet research · 2023
    Pooled it
  2. Article
  3. Article
  4. Community Review Boards offer a path to research equity.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  5. Article
  6. Review
  7. Review
  8. JAMIA open · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. 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

11 authors.

Erin RothwellThe University of Utah, Salt Lake City, USA.ORCID 0000-0002-2294-2299
Erin JohnsonThe University of Utah, Salt Lake City, USA.
Bob WongThe University of Utah, Salt Lake City, USA.
Aaron GoldenbergCase Western Reserve University, Cleveland, OH, USA.
Beth A TariniChildren's National Hospital, Washington, DC, USA.
Naomi RichesThe University of Utah, Salt Lake City, USA.ORCID 0000-0001-9815-6932
Louisa A StarkThe University of Utah, Salt Lake City, USA.
Christina PriesSpectrum Health System, Grand Rapids, MI, USA.
Carrie LangboInformedDNA, St. Petersburg, FL, USA.
Elizabeth LangenUniversity of Michigan, Ann Arbor, USA.
Jeffrey BotkinThe University of Utah, Salt Lake City, USA.

Funding

Utah Center for Clinical and Translational ScienceUL1TR002538 · NCATS · UNIVERSITY OF UTAH · PI HESS, RACHEL, MAJERSIK, JENNIFER JUHL · 2018 to 2022
$26.0M
Utah Center of Excellence in ELSI Research: UCEERRM1HG009037 · NHGRI · UNIVERSITY OF UTAH · PI ROTHWELL, ERIN, TABERY, JAMES · 2016 to 2024
$8.0M
The Effect of Electronic Informed Consent Information (EICI) on Residual Newborn Specimen ResearchR01HD082148 · NICHD · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Aaron J Goldenberg, ERIN ROTHWELL · 2015 to 2026
$5.1M
NCATS NIH HHS UL1 TR002538NHGRI NIH HHS RM1 HG009037NICHD NIH HHS R01 HD082148
6 · The paper itself

Abstract

Obtaining informed consent for bloodspot research from newborn screening is particularly challenging due to the hectic environment of the postnatal period and the relatively abstract nature of future, unspecified research on the biospecimens. A randomized controlled trial was conducted in three Michigan hospitals to compare two different consent processes (video and interactive tablet "app") with standard brochure-based consent in the Michigan BioTrust for Health. Results indicated higher knowledge scores for the video and app groups as well as significantly higher scores on satisfaction, amount of information, and clarity with the information provided. More research is needed to find the right amount of information for informed decision-making, and additional feasibility studies are needed to assess implementation strategies.

Indexed as

Mobile ApplicationsHumansInfant, NewbornInformed ConsentMichiganMultimediabiospecimensbloodspotsconsentmultimedianewborn screening

Identifiers

PMID32242760
PMCPMC7486234

What OpenQuestion holds

Textmetadata
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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.