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Lay REC members: patient or public?

Lay REC members: patient or public?

http://www.wikidata.org/entity/Q38093827

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A framework for public involvement at the design stage of NHS health and social care research: time to develop ethically conscious standards.Public involvement could usefully inform ethical review, but rarely does: what are the implications?

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Lay REC members: patient or public?

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MEDETHICS-2012-100642

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Journal of Medical Ethics

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Lay REC members: patient or public?

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Kristina Staley

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P2860

Research involving mental health consumers and carers: a reference group approach.

Service user involvement in nursing, midwifery and health visiting research: a review of evidence and practice.

Involving users in the design of a randomised controlled trial of an intervention to promote early presentation in breast cancer: qualitative study

Thrombolysis for acute ischaemic stroke: consumer involvement in design of new randomised controlled trial.

Ethical dilemmas in participatory action research: a case study from the disability community.

Quality improvement report: Improving design and conduct of randomised trials by embedding them in qualitative research: ProtecT (prostate testing for cancer and treatment) study. Commentary: presenting unbiased information to patients can be diffic

From passive subjects to equal partners: qualitative review of user involvement in research.

Involving consumers in designing, conducting, and interpreting randomised controlled trials: questionnaire survey.

Public involvement at the design stage of primary health research: a narrative review of case examples.

Exception from informed consent for pediatric resuscitation research: community consultation for a trial of brain cooling after in-hospital cardiac arrest.

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780-782

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scholarly article

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10.1136/MEDETHICS-2012-100642

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12

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2013-03-27T00:00:00Z

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23536688

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