Improvement of informed consent and the quality of consent documents (Q37153055)

18 August 2017

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title

Improvement of informed consent and the quality of consent documents (English)

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18 August 2017

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Michael Jefford

1

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author name string

Rosemary Moore

series ordinal

2

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PubMed ID

18452859

18 August 2017

language of work or name

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1 May 2008

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Lancet Oncology Commission

18 August 2017

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18 August 2017

9

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18 August 2017

5

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18 August 2017

485-493

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"In the interest of humanity and the cause of science": the yellow fever volunteers

18 August 2017

1 reference

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7 January 2021

What makes clinical research ethical?

1 reference

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7 January 2021

Is informed consent always necessary for randomized, controlled trials? .

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https://api.crossref.org/works/10.1016%2FS1470-2045%2808%2970128-1

7 January 2021

Consensus and controversy in clinical research ethics

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7 January 2021

Recommendations for informed consent forms for critical care clinical trials

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7 January 2021

Consent documents for oncology trials: does anybody read these things?

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7 January 2021

Informed consent -- why are its goals imperfectly realized?

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7 January 2021

The impact of disease severity on the informed consent process in clinical research.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2808%2970128-1

7 January 2021

Factors affecting quality of informed consent

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7 January 2021

Making sense of randomization; responses of parents of critically ill babies to random allocation of treatment in a clinical trial

1 reference

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7 January 2021

Patients' perceptions on informed consent and the quality of information disclosure in clinical trials.

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https://api.crossref.org/works/10.1016%2FS1470-2045%2808%2970128-1

7 January 2021

Informed consent for investigational chemotherapy: patients' and physicians' perceptions

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7 January 2021

The adequacy of consent forms for informing patients entering oncological clinical trials

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7 January 2021

Doctor-patient communication about breast cancer adjuvant therapy

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7 January 2021

Informed consent to biomedical research in Veterans Administration Hospitals

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7 January 2021

Quality of informed consent in cancer clinical trials: a cross-sectional survey

1 reference

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7 January 2021

Clinical cancer research--some aspects on doctors' attitudes to informing participants.

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7 January 2021

Randomized, controlled trial of an easy-to-read informed consent statement for clinical trial participation: a study of the Eastern Cooperative Oncology Group

1 reference

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7 January 2021

Communication and informed consent in phase 1 trials: a review of the literature.

1 reference

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7 January 2021

The ethics of randomised controlled trials from the perspectives of patients, the public, and healthcare professionals

1 reference

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7 January 2021

Quality of informed consent: a new measure of understanding among research subjects

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2808%2970128-1

7 January 2021

How do doctors explain randomised clinical trials to their patients?

1 reference

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7 January 2021

Communication of randomization in childhood leukemia trials

1 reference

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7 January 2021

Ethics of clinical trials.

1 reference

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7 January 2021

On the readability of surgical consent forms

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7 January 2021

Are informed consent forms that describe clinical oncology research protocols readable by most patients and their families?

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2808%2970128-1

7 January 2021

Readability of the public education literature on cancer prevention and detection

1 reference

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7 January 2021

Readability standards for informed-consent forms as compared with actual readability

1 reference

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7 January 2021

Health literacy and cancer communication

1 reference

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7 January 2021

Reading versus comprehension: implications for patient education and consent in an outpatient oncology clinic

1 reference

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7 January 2021

Evidence-based patient choice: a prostate cancer decision aid in plain language

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7 January 2021

Words matter: increasing the implementation of clinical guidelines

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2808%2970128-1

7 January 2021

Informed consent for clinical trials: a comparative study of standard versus simplified forms

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2808%2970128-1

7 January 2021

Can the written information to research subjects be improved?--an empirical study

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2808%2970128-1

7 January 2021

Longer consent forms for clinical trials compromise patient understanding: so why are they lengthening?

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2808%2970128-1

7 January 2021

Comprehension of informed consent information by young-old through old-old volunteers

1 reference

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7 January 2021

Improvement of the comprehension of written information given to healthy volunteers in biomedical research: a single-blind randomized controlled study

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2808%2970128-1

7 January 2021

Informed consent documents: increasing comprehension by reducing reading level

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2808%2970128-1

7 January 2021

The effect of format modifications and reading comprehension on recall of informed consent information by low-income parents: a comparison of print, video, and computer-based presentations

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2808%2970128-1

7 January 2021

Interventions to improve research participants' understanding in informed consent for research: a systematic review

1 reference

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7 January 2021

Telephone-based nursing intervention improves the effectiveness of the informed consent process in cancer clinical trials.

1 reference

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7 January 2021

Enhancing comprehension of information for informed consent: a review of empirical research.

1 reference

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7 January 2021

Improving informed consent in clinical trials: successful piloting of a decision aid

1 reference

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7 January 2021

Promoting patient participation and shortening cancer consultations: a randomised trial

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7 January 2021

Ethical, professional, and legal obligations in clinical practice: a series of discussion topics for postgraduate medical education. Introduction and topic 1: informed consent

1 reference

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7 January 2021

Developing ethical strategies to assist oncologists in seeking informed consent to cancer clinical trials

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7 January 2021

Seeking informed consent to cancer clinical trials; evaluating the efficacy of doctor communication skills training

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7 January 2021

The meaning and the measure of health literacy

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7 January 2021

Improving informed consent: suggestions from parents of children with leukemia

1 reference

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7 January 2021

Strategic physician communication and oncology clinical trials

1 reference

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7 January 2021

Understanding the decisions of cancer clinical trial participants to enter research studies: factors associated with informed consent, patient satisfaction, and decisional regret.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2808%2970128-1

7 January 2021

Patients' perceptions of information provided in clinical trials

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2808%2970128-1

7 January 2021

Improving comprehension for cancer patients with low literacy skills: strategies for clinicians.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2808%2970128-1

7 January 2021

Informed consent for clinical trials: is simpler better?

1 reference

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7 January 2021

10.1016/S1470-2045(08)70128-1

Identifiers

DOI

1 reference

18 August 2017

1 reference

PubMed ID

18452859