Lista de obras - Stuart G Nicholls - Dominio Público Uruguay

A Parent-Targeted and Mediated Video Intervention to Improve Uptake of Pain Treatment for Infants During Newborn Screening: A Pilot Randomized Controlled Trial

scientific article published on 01 January 2019

A Scoping Review of Empirical Research Relating to Quality and Effectiveness of Research Ethics Review.

artículo científico publicado en 2015

Antenatal Consultations at Extreme Prematurity: A Systematic Review of Parent Communication Needs

artículo científico publicado en 2017

Attitudes to incorporating genomic risk assessments into population screening programs: the importance of purpose, context and deliberation

artículo científico publicado en 2016

Benefits and burdens of newborn screening: public understanding and decision-making

artículo científico publicado en 2014

Call for a pan-Canadian approach to ethics review in Canada

article

Cluster over individual randomization: are study design choices appropriately justified? Review of a random sample of trials

scientific article published on 05 May 2020

Commentary on "Regulatory Support Improves Subsequent IRB/REC Approval Rates in Studies Initially Deemed Not Ready for Review: A CTSA Institution's Experience".

artículo científico publicado en 2018

Consent for newborn screening: parents' and health-care professionals' experiences of consent in practice

artículo científico publicado en 2016

Considering consent: a structural equation modelling analysis of factors influencing decisional quality when accepting newborn screening

artículo científico publicado en 2013

Developing a framework for the ethical design and conduct of pragmatic trials in healthcare: a mixed methods research protocol

article

Development of a robotic walker for individuals with cerebral palsy

scientific article published on 23 April 2019

Education and parental involvement in decision-making about newborn screening: understanding goals to clarify content.

artículo científico publicado en 2014

Establishing core outcome sets for phenylketonuria (PKU) and medium-chain Acyl-CoA dehydrogenase (MCAD) deficiency in children: study protocol for systematic reviews and Delphi surveys. ⬇️

artículo científico publicado en 2017

Ethical Issues in the Design and Conduct of Pragmatic Cluster Randomized Trials in Hemodialysis Care: An Interview Study With Key Stakeholders

scientific article published on 26 October 2020

Fiscal food policy: Equity and practice

artículo científico publicado en 2011

Genetic discrimination legislation in Canada: moving from rhetoric to real debate.

artículo científico publicado en 2016

Hospital Staff's Perceptions with Regards to the Baby-Friendly Initiative.

artículo científico publicado en 2016

Identification of translational dermatology research priorities in the U.K.: results of an electronic Delphi exercise

artículo científico publicado en 2015

Impact of stated barriers on proposed warfarin prescription for atrial fibrillation: a survey of Canadian physicians.

artículo científico publicado en 2014

Improving Service Evaluation in Clinical Genetics: Identifying Effects of Genetic Diseases on Individuals and Families

article

Informed choice for newborn blood spot screening in the United Kingdom: a survey of parental perceptions.

artículo científico publicado en 2012

Informed consent in pragmatic trials: results from a survey of trials published 2014–2019

artículo científico publicado en 2021

Intraoperative pharmacologic opioid minimisation strategies and patient-centred outcomes after surgery: a scoping review protocol

artículo científico publicado en 2023

La déclaration RECORD-PE (Reporting of Studies Conducted Using Observational Routinely Collected Health Data Statement for Pharmacoepdemiology) : directives pour la communication des études realisées à partir de données de santé observationelles col

artículo científico publicado en 2019

Neuroprotective Core Measure 5: Minimizing Stress and Pain—Neonatal Pain Management Practices During Heel Lance and Venipuncture in Ontario, Canada

article

Of Parachutes and Participant Protection: Moving Beyond Quality to Advance Effective Research Ethics Oversight

scientific article published on 12 December 2018

Outcome measurement in clinical genetics services: a systematic review of validated measures.

artículo científico publicado en 2008

Outcome measures for clinical genetics services: A comparison of genetics healthcare professionals and patients’ views

article

Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a review

artículo científico publicado en 2020

Pain Management During Newborn Screening: Using YouTube to Disseminate Effective Pain Management Strategies.

artículo científico publicado en 2017

Parental decision-making and acceptance of newborn bloodspot screening: an exploratory study

artículo científico publicado en 2013

Parental information use in the context of newborn bloodspot screening. An exploratory mixed methods study.

artículo científico publicado en 2012

Parents' evaluation of the IDEFICS intervention: an analysis focussing on socio-economic factors, child's weight status and intervention exposure

artículo científico

Patient empowerment in clinical genetics services.

artículo científico publicado en 2008

Proceduralisation, choice and parental reflections on decisions to accept newborn bloodspot screening ⬇️

artículo científico publicado el 20 de diciembre de 2011

Public attitudes towards genomic risk profiling as a component of routine population screening

artículo científico publicado en 2013

Reporting of consent rates in critical care studies: room for improvement

artículo científico

Reporting of key methodological and ethical aspects of cluster trials in hemodialysis require improvement: a systematic review

artículo científico publicado en 2020

Reporting transparency: making the ethical mandate explicit

artículo científico publicado en 2016

Review of pragmatic trials found that multiple primary outcomes are common but so too are discrepancies between protocols and final reports

artículo científico publicado en 2021

Routinely collected data: the importance of high-quality diagnostic coding to research

artículo científico publicado en 2017

Screening for depression in women during pregnancy or the first year postpartum and in the general adult population: a protocol for two systematic reviews to update a guideline of the Canadian Task Force on Preventive Health Care

article

Stakeholder attitudes towards the role and application of informed consent for newborn bloodspot screening: a study protocol

artículo científico publicado en 2014

Stakeholder views regarding ethical issues in the design and conduct of pragmatic trials: study protocol

artículo científico publicado en 2018

Standards and classification: A perspective on the ‘obesity epidemic’

scientific article published on 18 March 2013

The Human Genome Project, and recent advances in personalized genomics

artículo científico publicado en 2015

The Importance of Describing as Well as Defining Usual Care

scientific article published on 01 January 2020

The RECORD reporting guidelines: meeting the methodological and ethical demands of transparency in research using routinely-collected health data

artículo científico publicado en 2016

The REporting of Studies Conducted Using Observational Routinely-Collected Health Data (RECORD) Statement: Methods for Arriving at Consensus and Developing Reporting Guidelines

artículo científico publicado en 2015

The emotional effects of genetic diseases: Implications for clinical genetics

article

The ethical challenges raised in the design and conduct of pragmatic trials: an interview study with key stakeholders

artículo científico publicado en 2019

The need for ethics as well as evidence in evidence-based medicine

artículo científico publicado en 2016

The reporting of studies conducted using observational routinely collected health data statement for pharmacoepidemiology (RECORD-PE)

artículo científico publicado en 2018

Too many crying babies: a systematic review of pain management practices during immunizations on YouTube.

artículo científico publicado en 2014

Using YouTube to Disseminate Effective Vaccination Pain Treatment for Babies

artículo científico publicado en 2016

What is in a Name? Parent, Professional and Policy-Maker Conceptions of Consent-Related Language in the Context of Newborn Screening

scientific article published on 04 May 2019

What outcomes are important in the recovery from acromio-clavicular (AC) joint pathology? A focus group study with patients and surgeons

artículo científico publicado en 2020

What process attributes of clinical genetics services could maximise patient benefits?

artículo científico publicado en 2008

Lista de obras de Stuart G Nicholls

A Parent-Targeted and Mediated Video Intervention to Improve Uptake of Pain Treatment for Infants During Newborn Screening: A Pilot Randomized Controlled Trial

A Scoping Review of Empirical Research Relating to Quality and Effectiveness of Research Ethics Review.

Antenatal Consultations at Extreme Prematurity: A Systematic Review of Parent Communication Needs

Attitudes to incorporating genomic risk assessments into population screening programs: the importance of purpose, context and deliberation

Benefits and burdens of newborn screening: public understanding and decision-making

Call for a pan-Canadian approach to ethics review in Canada

Cluster over individual randomization: are study design choices appropriately justified? Review of a random sample of trials

Commentary on "Regulatory Support Improves Subsequent IRB/REC Approval Rates in Studies Initially Deemed Not Ready for Review: A CTSA Institution's Experience".

Consent for newborn screening: parents' and health-care professionals' experiences of consent in practice

Considering consent: a structural equation modelling analysis of factors influencing decisional quality when accepting newborn screening

Developing a framework for the ethical design and conduct of pragmatic trials in healthcare: a mixed methods research protocol

Development of a robotic walker for individuals with cerebral palsy

Education and parental involvement in decision-making about newborn screening: understanding goals to clarify content.

Establishing core outcome sets for phenylketonuria (PKU) and medium-chain Acyl-CoA dehydrogenase (MCAD) deficiency in children: study protocol for systematic reviews and Delphi surveys. ⬇️

Ethical Issues in the Design and Conduct of Pragmatic Cluster Randomized Trials in Hemodialysis Care: An Interview Study With Key Stakeholders

Fiscal food policy: Equity and practice

Genetic discrimination legislation in Canada: moving from rhetoric to real debate.

Hospital Staff's Perceptions with Regards to the Baby-Friendly Initiative.

Identification of translational dermatology research priorities in the U.K.: results of an electronic Delphi exercise

Impact of stated barriers on proposed warfarin prescription for atrial fibrillation: a survey of Canadian physicians.

Improving Service Evaluation in Clinical Genetics: Identifying Effects of Genetic Diseases on Individuals and Families

Informed choice for newborn blood spot screening in the United Kingdom: a survey of parental perceptions.

Informed consent in pragmatic trials: results from a survey of trials published 2014–2019

Intraoperative pharmacologic opioid minimisation strategies and patient-centred outcomes after surgery: a scoping review protocol

La déclaration RECORD-PE (Reporting of Studies Conducted Using Observational Routinely Collected Health Data Statement for Pharmacoepdemiology) : directives pour la communication des études realisées à partir de données de santé observationelles col

Neuroprotective Core Measure 5: Minimizing Stress and Pain—Neonatal Pain Management Practices During Heel Lance and Venipuncture in Ontario, Canada

Of Parachutes and Participant Protection: Moving Beyond Quality to Advance Effective Research Ethics Oversight

Outcome measurement in clinical genetics services: a systematic review of validated measures.

Outcome measures for clinical genetics services: A comparison of genetics healthcare professionals and patients’ views

Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a review

Pain Management During Newborn Screening: Using YouTube to Disseminate Effective Pain Management Strategies.

Parental decision-making and acceptance of newborn bloodspot screening: an exploratory study

Parental information use in the context of newborn bloodspot screening. An exploratory mixed methods study.

Parents' evaluation of the IDEFICS intervention: an analysis focussing on socio-economic factors, child's weight status and intervention exposure

Patient empowerment in clinical genetics services.

Proceduralisation, choice and parental reflections on decisions to accept newborn bloodspot screening ⬇️

Public attitudes towards genomic risk profiling as a component of routine population screening

Reporting of consent rates in critical care studies: room for improvement

Reporting of key methodological and ethical aspects of cluster trials in hemodialysis require improvement: a systematic review

Reporting transparency: making the ethical mandate explicit

Review of pragmatic trials found that multiple primary outcomes are common but so too are discrepancies between protocols and final reports

Routinely collected data: the importance of high-quality diagnostic coding to research

Screening for depression in women during pregnancy or the first year postpartum and in the general adult population: a protocol for two systematic reviews to update a guideline of the Canadian Task Force on Preventive Health Care

Stakeholder attitudes towards the role and application of informed consent for newborn bloodspot screening: a study protocol

Stakeholder views regarding ethical issues in the design and conduct of pragmatic trials: study protocol

Standards and classification: A perspective on the ‘obesity epidemic’

The Human Genome Project, and recent advances in personalized genomics

The Importance of Describing as Well as Defining Usual Care

The RECORD reporting guidelines: meeting the methodological and ethical demands of transparency in research using routinely-collected health data

The REporting of Studies Conducted Using Observational Routinely-Collected Health Data (RECORD) Statement: Methods for Arriving at Consensus and Developing Reporting Guidelines

The emotional effects of genetic diseases: Implications for clinical genetics

The ethical challenges raised in the design and conduct of pragmatic trials: an interview study with key stakeholders

The need for ethics as well as evidence in evidence-based medicine

The reporting of studies conducted using observational routinely collected health data statement for pharmacoepidemiology (RECORD-PE)

Too many crying babies: a systematic review of pain management practices during immunizations on YouTube.

Using YouTube to Disseminate Effective Vaccination Pain Treatment for Babies

What is in a Name? Parent, Professional and Policy-Maker Conceptions of Consent-Related Language in the Context of Newborn Screening

What outcomes are important in the recovery from acromio-clavicular (AC) joint pathology? A focus group study with patients and surgeons

What process attributes of clinical genetics services could maximise patient benefits?