[PDF] Top 20 Obtaining consent for neonatal research
Has 10000 "Obtaining consent for neonatal research" found on our website. Below are the top 20 most common "Obtaining consent for neonatal research".
Obtaining consent for neonatal research
... in Research (CERES) (9) and the Cochrane Collaboration Consumer Network (10) show that we should not neglect “demand side” ...non-consensual research might first be put out to community consultation (an ... See full document
12
Retrospective Consent in a Neonatal Randomized Controlled Trial
... parental consent (Era 1) with the later era when either prospective or retrospective consent could be used (Era ...for consent in the first few days after birth, at a time judged to be appropriate by ... See full document
9
Securing recruitment and obtaining informed consent in minority ethnic groups in the UK
... informed consent is a requirement for all research studies within the NHS, and strict guidance on patient information sheets and consent forms is given by the National Research Ethics Service ... See full document
9
The publication of ethically uncertain research: attitudes and practices of journal editors
... regarding obtaining informed consent or research ethics board (REB) approval and the majority of editors did not instruct the reviewers to con- sider ethical issues in their assessments of submitted ... See full document
6
Perspectives on Informed Consent Practices for Minimal-Risk Research Involving Foster Youth
... for obtaining informed consent for youth in foster care to participate in minimal-risk research; a review of 49 publications revealed 14 different combinations of individuals used for informed ... See full document
5
Fifteen minute consultation: An evidence based approach to research without prior consent (deferred consent) in neonatal and paediatric critical care trials
... Emergency research with critically unwell children is vital to make sure that the most ill and injured children benefit from evidence-based ...that consent be sought from parents (or legal representatives) ... See full document
7
Honesty, Trust, and Respect During Consent Discussions in Neonatal Clinical Trials
... whose research participation is sought are often immature or ill, study staff must be exquisitely sensitive to the current stress and vulnerability of the ...for consent understands the scienti fi c ... See full document
5
When Is Waiver of Consent Appropriate in a Neonatal Clinical Trial?
... This research differs from research that is designed to evaluate new ...with research but expose many more patients to the comparable risks of idiosyncratic practice ...the research itself ... See full document
9
Ethical frameworks for obtaining informed consent in tumour profiling: an evidence-based case for Singapore
... broad consent model where participants would not con- sent to specific projects or types of ...would consent altruis- tically on the condition that their data is used for re- search that has the potential ... See full document
11
N.
... and obtaining their consent for participation in the study, all mothers who delivered will be interviewed to assess various traditional and cultural practices followed during neonatal ... See full document
6
Can obtaining informed consent alter self-reported drinking behaviour? A methodological experiment
... answering research ques- tions in an unbiased manner, including in evaluations of intervention ...informed consent undertaken in RCTs and other types of studies may diminish impact on participant’s ... See full document
7
When Is Waiver of Consent Appropriate in a Neonatal Clinical Trial?
... rigorous research on treatments that must be administered urgently or ...base. Research would be facilitated if it were permissible to waive the requirement for parental ...for consent but only if ... See full document
7
Obtaining Consent from Both Parents for Pediatric Research: What Does “Reasonably Available” Mean?
... On the basis of these consultations, we established procedures for de- termining father availability, outlined in Fig 1. Once eligible mothers agreed to participate, RAs determined if absent fathers were involved and/or ... See full document
9
Procedures of recruiting, obtaining informed consent, and compensating research participants in Qatar: findings from a qualitative investigation
... services research pose challenges and opportunities ...informed consent becomes based on Western ethical standards ...and consent procedures among culturally diverse groups in non-Western countries ... See full document
13
Lessons learned obtaining informed consent in research with vulnerable populations in community health center settings
... of obtaining ac- curate contact information and reaching CHC patients by phone has implications for providing quality clinical care as well as for equitable representation in research ... See full document
13
The acceptability of conducting data linkage research without obtaining consent: lay people’s views and justifications
... the consent preference were the same or similar to the views expressed in Scenario ...for consent but some justifications related specifically to information about deceased ...seeking consent is a ... See full document
16
Impact of social stigma on the process of obtaining informed consent for genetic research on podoconiosis: a qualitative study
... genetic research; role of stigma in risk perception, motivation and decision mak- ing for participation in genetic research; and place of trust in the consent ... See full document
10
Conflict + (and) Interest: Financial Incentives and Informed Consent in Human Subject Research
... With the recent attention to the issue of patient protection in clinical research in general, and disclosure of financial incen- tives in obtaining informed consent [r] ... See full document
37
More Information, Less Understanding: A Randomized Study on Consent Issues in Neonatal Research
... explore differences between groups. There was limited understanding about the background and purpose of the study, particularly in those receiving the US leaflet with- out verbal explanation. There were significant ... See full document
7
Prevention of Infections in Cardiac Surgery study (PICS): study protocol for a pragmatic cluster randomized factorial crossover pilot trial
... Thirdly, obtaining consent from individual participants for the antibiotic prophylaxis strategy would not be feas- ible in a cluster randomized controlled trial, as the protocol would need to be applied to ... See full document
8
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