Cited by 137Ethics in Clinical ResearchHealthcare Decision-Making and RestraintsEthics and bioethics in healthcare

Caring about risks: are severely depressed patients competent to consent to research

Elliott, Carl·1997·Archives of General Psychiatry

Abstract

Depressed patients are often asked to take part in clinical research studies that carry risk. These patients are generally assumed to be mentally competent to consent to research, since depression often leaves a patient's cognitive abilities intact. In this article, it is argued that many severely depressed patients may not be competent to consent because they cannot be considered accountable for their decisions. The article presents 2 arguments: first, that it is unclear whether the decisions of some severely depressed patients are authentically theirs, and second, that some severely depressed patients may not have the appropriate minimal degree of concern for their own well-being. It is argued that assessments of competence must take account of emotional factors, and that, if severely depressed patients are incompetent to consent, research studies involving a poor risk-benefit ratio will be much more difficult to justify.

Integrity signals

Registry

Crossref · 10.1001/archpsyc.1997.01830140021003

Cites

25 of 25 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Elliott, C.
Affiliations
McGill University (CA)
Corresponding author
Elliott, Carl
Venue
Archives of General Psychiatry
Published
1997-02-01
Volume
54
Issue
2
Pages
113
ISSN
0003-990X (ISSN-L)
OpenAlex
W1969879975
Cited by
137
References
25
Citations by year
2025: 2 · 2024: 5 · 2023: 5 · 2022: 2 · 2021: 2 · 2020: 2 · 2019: 3 · 2018: 16 · 2017: 7 · 2016: 4 · 2015: 4 · 2014: 4 · 2013: 6 · 2012: 2
FWCI
7.83
Type
journal article
Language
en
Open access
closed
Locations
  • Archives of General Psychiatry (publishedVersion)
  • PubMed (publishedVersion)
  • DigitalGeorgetown (Georgetown University Library) (submittedVersion)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Ethics in Clinical Research
  • Social Sciences › Psychology › Clinical Psychology › Healthcare Decision-Making and Restraints
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Ethics and bioethics in healthcare
Keywords
severe depression, informed consent, research participation, decision-making capacity, self-care, risk-benefit ratio, clinical research ethics
MeSH terms
Depressive Disorder, Ethics, Medical, Humans, Human Experimentation, Informed Consent, Research Design, Severity of Illness Index, Mental Competency, Risk Assessment

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review