Evidence map›Paper›PMID 11834759›Full record

ArticleJournal of medical ethics2002

It doesn't cost anything just to ask, does it? The ethics of questionnaire-based research.

M Evans, M Robling, F Maggs Rapport, H Houston, P Kinnersley, C Wilkinson

Abstract read
In one paragraph

Article in Journal of medical ethics, 2002. 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. Article
  5. Article
  6. Article
  7. Confidentiality and the ethics of medical ethics.Journal of medical ethics · 2003
    Article
  8. The cost of questionnaire based research.Journal of epidemiology and community health · 2002
    Review
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.

M EvansCentre for Philosophy and Health Care, University of Wales, Swansea, Wales, UK.
M Robling
F Maggs Rapport
H Houston
P Kinnersley
C Wilkinson

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patient-based outcome measures are increasingly important in health care evaluations, often through the use of paper-based questionnaires. The likely impact of questionnaires upon patients is not often considered and therefore, the balance of benefit and harm not fully explored. Harms that might accrue for research staff are even less frequently considered. This paper describes the use of postal questionnaires within a study of breast disease management in primary care. Questionnaire responses are used to describe the nature of discomfort or harms that may occur in such studies. Ethical issues raised by the harms are discussed in relation to the benefits of the study. Practical suggestions for reducing harm to patients are proposed. A secondary consideration, discomfort to the researcher, is also identified and suggestions made to reduce its effect. Finally, the role of research questionnaires as a study intervention is discussed.

Indexed as

Biomedical ResearchEthics, ClinicalEthics, ResearchBreast DiseasesCase-Control StudiesCross-Sectional StudiesFamily PracticeFemaleHumansPatientsReferral and ConsultationRisk AssessmentRisk FactorsSensitivity and SpecificitySurveys and QuestionnairesUnited KingdomBiomedical and Behavioral Research

Identifiers

PMID11834759
PMCPMC1733515

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.