Cargando…

An ethnographic study of group decision making to understand and improve how trial steering committees contribute to trial conduct

Detalles Bibliográficos
Autores principales:	Daykin, Anne, Heawood, Ali, Lane, Athene, Macefield, Rhiannon, Gamble, Carrol, McCann, Sharon, Shorter, Gillian, Sydes, Matthew R
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2013
Materias:	Oral Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3980686/ http://dx.doi.org/10.1186/1745-6215-14-S1-O79

Ejemplares similares

What are the roles and valued attributes of a Trial Steering Committee? Ethnographic study of eight clinical trials facing challenges
por: Daykin, Anne, et al.
Publicado: (2016)

‘We all want to succeed, but we’ve also got to be realistic about what is happening’: an ethnographic study of relationships in trial oversight and their impact
por: Daykin, Anne, et al.
Publicado: (2017)

Enhancing public involvement in trial oversight committees through qualitative research with eight trials facing challenges
por: Nicholson, A, et al.
Publicado: (2015)

Exploring the role and functionality of trial steering committees
por: Harman, Nicola, et al.
Publicado: (2015)

A cohort examination to establish reporting of the remit and function of Trial Steering Committees in randomised controlled trials
por: Conroy, Elizabeth J., et al.
Publicado: (2017)

A review of the description of patient withdrawal in trial protocols and patient information sheets (PIS)
por: Kearney, Anna, et al.
Publicado: (2015)

“To have, to hold, from this day forward”: understanding current practice regarding the retention of trial participants
por: Daykin, Anne, et al.
Publicado: (2015)

Understanding and optimising patient and public involvement in trial oversight: an ethnographic study of eight clinical trials
por: Coulman, K. D., et al.
Publicado: (2020)

A third trial oversight committee: Functions, benefits and issues
por: Lane, J Athene, et al.
Publicado: (2019)

Reported reasons for missing data and the interplay with trial setting
por: Kearney, Anna, et al.
Publicado: (2015)

Exploring the role and function of trial steering committees: results of an expert panel meeting
por: Harman, Nicola L., et al.
Publicado: (2015)

Pragmatic approaches to mitigating missing data and research priorities to assess the effectiveness of interventions
por: Kearney, Anna, et al.
Publicado: (2015)

Reporting remit and function of trial steering committees in randomised controlled trials: review of published literature
por: Conroy, EJ, et al.
Publicado: (2015)

Evaluation of source data verification in a multicentre cancer trial (PROTECT)
por: Lane, J Athene, et al.
Publicado: (2013)

Trial steering committees for randomised controlled trials: updating and redeveloping guidance and terms of reference informed by current practice and experience
por: Conroy, EJ, et al.
Publicado: (2013)

The use of systematic reviews in the planning, design and conduct of randomised trials: a retrospective cohort of NIHR HTA funded trials
por: Jones, Ashley, et al.
Publicado: (2013)

‘Recruitment, recruitment, recruitment’ – the need for more focus on retention: a qualitative study of five trials
por: Daykin, Anne, et al.
Publicado: (2018)

Identifying research priorities for effective retention strategies in clinical trials
por: Kearney, Anna, et al.
Publicado: (2017)

Remits, roles and working models for trial steering committees and data monitoring committees in studies evaluating diagnostic tests: a survey of current practice
por: Ferrante di Ruffano, Lavinia, et al.
Publicado: (2013)

Evidence base for patient and public involvement in clinical trials (EPIC)
por: Gamble, Carrol, et al.
Publicado: (2013)

Recruitment and retention in internet based randomised trials
por: Shorter, Gillian W, et al.
Publicado: (2013)

Reducing attrition within clinical trials: The communication of retention and withdrawal within patient information leaflets
por: Kearney, Anna, et al.
Publicado: (2018)

Recruitment to trials: insights from a meta-ethnography of qualitative studies
por: McCann, Sharon, et al.
Publicado: (2013)

Opening research sites in multicentre clinical trials within the UK: a detailed analysis of delays
por: Williamson, Paula, et al.
Publicado: (2013)

Realising the potential of patient and public involvement to make a difference: what can trial teams do?
por: Young, Bridget, et al.
Publicado: (2015)

The importance of rapport and relationship building when recruiting to clinical trials: a qualitative investigation of trial recruitment consultations in a surgical RCT
por: Constable, Lynda, et al.
Publicado: (2015)

The value of evidence synthesis in randomised controlled trial (RCT) design, conduct and analysis: MRC clinical trials unit (CTU) at UCL experience
por: Tierney, Jayne F, et al.
Publicado: (2015)

Optimising the design and evaluation of pilot work to inform the main trial: a review of current evidence and consideration of future practices
por: O'Connell Francischetto, Elaine, et al.
Publicado: (2013)

Service user groups as co-applicants on a platform study for a trial
por: Morgan, Heather, et al.
Publicado: (2013)

Development of guidance for statistical analysis plans (SAPs) for clinical trials
por: Krishan, Ashma, et al.
Publicado: (2015)

Guidance to detect, evaluate and prevent the problem of selective reporting in trial publications
por: Dwan, Kerry, et al.
Publicado: (2013)

Evaluating best practice in informed consent discussions: a new method of evaluating information provision and patient understanding during trial recruitment consultations
por: Wade, Julia, et al.
Publicado: (2013)

Selective reporting in clinical trials - an examination of discrepancy rates in pre-specified and reported outcomes in articles submitted to the BMJ
por: Weston, Jennifer, et al.
Publicado: (2015)

Improving the quality of data in clinical trials in cancer. COMPACT Steering Committee.
Publicado: (1991)

The natural history of conducting and reporting clinical trials: interviews with trialists
por: Smyth, Rebecca MD, et al.
Publicado: (2015)

A framework for the design and analysis of phase III randomised trials in uncommon diseases
por: Parmar, Mahesh, et al.
Publicado: (2015)

Prospective reporting of statistical analysis plans for randomised controlled trials
por: Hemming, Karla, et al.
Publicado: (2020)

Methods for selecting health concepts and domains from in-depth qualitative interviews for the development of patient reported outcome measures (PROMS): a case study
por: Blazeby, Jane, et al.
Publicado: (2015)

The use of systematic reviews in the planning, design and conduct of randomised trials: a retrospective cohort of NIHR HTA funded trials
por: Jones, Ashley P, et al.
Publicado: (2013)

Clinical trials registries: is it viable for the inclusion of conduct, performance, analyses and cost of trials?
por: Young, Amanda, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_qpld1m4osd7tnt6soi4u4l2c5f