Evidence map›Paper›PMID 26709381›Full record

ArticleAJOB empirical bioethics

Cancer clinical trial participants' assessment of risk and benefit.

Connie M Ulrich, Sarah J Ratcliffe, Gwenyth R Wallen, Qiuping Pearl Zhou, Kathleen Knafl, Christine Grady

Abstract read
In one paragraph

Article in AJOB empirical bioethics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 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

15 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Motivations and Decision-Making of Adult Sickle Cell Patients in High-Risk Clinical Research.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2020
    Article
  9. Article
  10. Assessment of adherence and relative dose intensity with oral chemotherapy in oncology clinical trials at an academic medical center.Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners · 2018
    Article
  11. Article
  12. Article
  13. Article
  14. Which Benefits Are Mentioned Most Often in Drug Development Publications?Current therapeutic research, clinical and experimental
    Article
  15. 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

6 authors.

Connie M UlrichDepartment of Biobehavioral Health Sciences and Department of Medical Ethics and Health Policy, University of Pennsylvania School of Nursing and Perelman School of Medicine.
Sarah J RatcliffeDepartment of Biostatistics & Epidemiology, University of Pennsylvania Perelman School of Medicine.
Gwenyth R WallenNational Institutes of Health Clinical Center.
Qiuping Pearl ZhouDepartment of Nursing, George Washington University.
Kathleen KnaflDivision of Family Health, University of North Carolina School of Nursing Chapel Hill.
Christine GradyDepartment of Bioethics, National Institutes of Health.

Funding

Respondent Burden and Retention in Cancer Clinical TrialsR21NR010259 · NINR · UNIVERSITY OF PENNSYLVANIA · PI ULRICH, CONNIE MARIE · 2008 to 2009
$433k
Intramural NIH HHS Z99 CL999999NINR NIH HHS R21 NR010259
6 · The paper itself

Abstract

backgroundThe purpose of this article is to examine the extent to which cancer clinical trial participants assess the benefits and risks of research participation before enrollment.

methodsOne hundred and ten oncology research participants enrolled in cancer clinical research in a large Northeastern cancer center responded to a self-administered questionnaire on perceptions about cancer clinical trials.

resultsOf the participants, 51.6% reported they did not directly assess the benefits or risks. Educational level, age, employment, treatment options, insurance, and spiritual-religious beliefs were significantly associated with whether participants assessed risk and benefits. Those who felt well informed were more likely to have assessed the benefits and risks at enrollment than those who did not feel well informed (odds ratio [OR] = 3.92,

conclusionOur findings have important implications for understanding the role of assessing risks and benefits in the research participation decisions of patients with cancer and call for further understanding of why participants are not assessing information believed to be essential for autonomous informed decisions.

Indexed as

cancerclinical trialsinformed consentrisks and benefits

Identifiers

PMID26709381
PMCPMC4689188

What OpenQuestion holds

Textmetadata
LicenceTDM
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.