Patients' perceptions of information provided in clinical trials. - Wikidata - wikimedia - TriplyDB

Patients' perceptions of information provided in clinical trials.

Patients' perceptions of information provided in clinical trials.

http://www.wikidata.org/entity/Q35423226

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A survey of study participants' understanding of informed consent to participate in a randomised controlled trial of acupuncture Recruiting ethnic minority participants to a clinical trial: a qualitative study.Protection of children in research."Cold calling" in psychiatric follow up studies: is it justified?Informed consent in oncology clinical trials: A Brown University Oncology Research Group prospective cross-sectional pilot study Measuring the process and quality of informed consent for clinical research: development and testing.Views of clinical trial participants on the readability and their understanding of informed consent documents.Recall of informed consent information by healthy volunteers in clinical trials.Continuing review of ethics in clinical trials: a surveillance study in Iran What information and the extent of information research participants need in informed consent forms: a multi-country survey

P2860

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P2860

Patients' perceptions of information provided in clinical trials.

http://www.wikidata.org/entity/Q35423226

description

2002 nî lūn-bûn

@nan

2002 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2002年の論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年论文

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name

Patients' perceptions of information provided in clinical trials.

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Patients' perceptions of information provided in clinical trials.

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type

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Patients' perceptions of information provided in clinical trials.

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Patients' perceptions of information provided in clinical trials.

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Patients' perceptions of information provided in clinical trials.

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Patients' perceptions of information provided in clinical trials.

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P1433

Journal of Medical Ethics

P1476

Patients' perceptions of information provided in clinical trials.

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P R Ferguson

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P2860

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

Random allocation or allocation at random? Patients' perspectives of participation in a randomised controlled trial.

Reactions of participants to the results of a randomised controlled trial: exploratory study.

The problem of informed consent in emergency medicine research.

Informed consent: study of quality of information given to participants in a clinical trial.

Are patient consent forms for research protocols easy to read?

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

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

Local Research Ethics Committees can audit ethical standards in research.

Offering patients entry in clinical trials: preliminary study of the views of prospective participants.

P304

45-48

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scholarly article

P356

10.1136/JME.28.1.45

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1

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28

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2002-02-01T00:00:00Z

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11525594

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11834760

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1733530

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