Katie Gillies

kewarganegaraan: Britania Raya

pekerjaan: peneliti, ilmuwan

laman resmi: abdn.pure.elsevier.com/en/en/persons/kate-gillies(fca559b7-f3f7-4624-bfd6-a98d89429486).html

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Artikel 30

Date

Judul

Pengarang

2022-02

Developing an online, searchable database to systematically map and organise current literature on retention research (ORRCA2)

Edward Stanhope, Anna Kearney, William J Cragg, Andrew Hunter, Heidi R Gardner, Nicola L. Harman, Daisy Gaunt, Katie Gillies, Declan Devane, Akke Vellinga, Athene Lane, Carrol Gamble
2021-02-27

An international core outcome set for evaluating interventions to improve informed consent to clinical trials: The ELICIT Study

Katie Gillies, Heidi R Gardner, Shaun Treweek, Marion K Campbell
2020-02-02

Dissemination of trial results to participants in phase III pragmatic clinical trials: an audit of trial investigators intentions

Katie Gillies
2020-01-07

Trial Forge Guidance 2: how to decide if a further Study Within A Trial (SWAT) is needed

Shaun Treweek, Declan Devane, Frank Sullivan, Erik von Elm, Mike Clarke, Kerenza Hood, Heidi R Gardner, Adwoa Hughes-Morley, Roberta Littleford, Katie Gillies, Matthias Briel, Craig R Ramsay, Marion K Campbell, Peter Bower
2020-11-16

A systematic review of risk communication in clinical trials: How does it influence decisions to participate and what are the best methods to improve understanding in a trial context?

Katie Gillies
2019-10-15

What are the most important unanswered research questions in trial retention? A James Lind Alliance Priority Setting Partnership: the PRioRiTy II (Prioritising Retention in Randomised Trials) study

Declan Devane, Katie Gillies, Kerenza Hood
2019-10-28

Reducing research waste by promoting informed responses to invitations to participate in clinical trials

Katie Gillies, Paul P. Glasziou
2019-11-09

Designing and using incentives to support recruitment and retention in clinical trials: a scoping review and a checklist for design

Beth Parkinson, Matt Sutton, Eleonora Fichera, Gillian W Shorter, Peter Bower, Nicola L. Harman, Nicola Mills, Katie Gillies
2019-07-05

Development and evaluation of decision aids for people considering taking part in a clinical trial: a conceptual framework

Katie Gillies
2019-06-03

Exploring non-retention in clinical trials: a meta-ethnographic synthesis of studies reporting participant reasons for drop out

Katie Gillies
2018-02-23

Trial Forge Guidance 1: what is a Study Within A Trial (SWAT)?

Shaun Treweek, Adwoa Hughes-Morley, Declan Devane, Frank Sullivan, Ella Flemyng, Paula Williamson, Mike Clarke, Peter Bower, Seonaidh Cotton, Katie Gillies, Roberta Littleford, Craig R Ramsay, Sandra Galvin, Heidi R Gardner
2018-03-27

Systematic Techniques to Enhance rEtention in Randomised controlled trials: the STEER study protocol.

Katie Gillies, Shaun Treweek
2018-06-27

Patient reported measures of informed consent for clinical trials: A systematic review.

Katie Gillies
2018-09-05

Relative importance of informational items in participant information leaflets for trials: a Q-methodology approach

Katie Gillies
2018-09-07

Prioritizing research areas for antibiotic stewardship programmes in hospitals: a behavioural perspective consensus paper

Esmita Charani, Eilidh M Duncan, Katie Gillies, Charis A Marwick, Ralph Möhler, Susan Rogers Van Katwyk, Jan Clarkson
2018-09-06

Surgeons' and methodologists' perceptions of utilising an expertise-based randomised controlled trial design: a qualitative study

Jonathan A. Cook, Katie Gillies
2017-08-11

'It's trying to manage the work': a qualitative evaluation of recruitment processes within a UK multicentre trial

Katie Gillies, Shaun Treweek
2016-01-08

Vaginal birth after caesarean section: why is uptake so low? Insights from a meta-ethnographic synthesis of women's accounts of their birth choices

Katie Gillies, Vikki A. Entwistle, Siladitya Bhattacharya
2015-11-27

Decision aids for people considering taking part in clinical trials

Katie Gillies, Mary Politi, Jamie C Brehaut
2015-10-27

Evaluation of interventions for informed consent for randomised controlled trials (ELICIT): protocol for a systematic review of the literature and identification of a core outcome set using a Delphi survey

Katie Gillies, Vikki A. Entwistle, Shaun Treweek, Paula Williamson
2015-06-05

Making randomised trials more efficient: report of the first meeting to discuss the Trial Forge platform

Shaun Treweek, Kirsty Loudon, Matthew R Sydes, Daniel Shanahan, Peter Craig, Annmarie Nelson, Janet A Dunn, Declan Devane, Iain Chalmers, Carrol Gamble, Diana Elbourne, Paula Williamson, Gladys McPherson, Trudie Lang, Lelia Duley, Mike Clarke, Kerenza Hood, Douglas G. Altman, Peter Bower, Seonaidh Cotton, Katie Gillies, Roberta Littleford, Craig R Ramsay
2015-05-18

Medical expulsive therapy in adults with ureteric colic: a multicentre, randomised, placebo-controlled trial

Katie Gillies, Mary Kilonzo, Gladys McPherson
2014-07-30

Making a decision about trial participation: the feasibility of measuring deliberation during the informed consent process for clinical trials

Glyn Elwyn, Katie Gillies, Jonathan A. Cook
2014-08-19

Decision aids for randomised controlled trials: a qualitative exploration of stakeholders' views

Katie Gillies
2014-02-18

Patient information leaflets (PILs) for UK randomised controlled trials: a feasibility study exploring whether they contain information to support decision making about trial participation

Katie Gillies, Jamie C Brehaut
2013-11-04

Determining information for inclusion in a decision-support intervention for clinical trial participation: a modified Delphi approach

Katie Gillies, Sara MacLennan
2012-03-14

Decision support interventions for people making decisions about participation in clinical trials

Katie Gillies, Jamie C Brehaut, Mary Politi
2012-11-05

Antimicrobial catheters for reduction of symptomatic urinary tract infection in adults requiring short-term catheterisation in hospital: a multicentre randomised controlled trial.

Katie Gillies, Mary Kilonzo, Jennifer Burr, Brian S Buckley, Gladys McPherson
2012-08-08

Supporting positive experiences and sustained participation in clinical trials: looking beyond information provision

Katie Gillies, Vikki A. Entwistle
2011-12-13

Analysis of patient information leaflets (PILs), used in clinical trials using the Informed Consent Evaluation instrument (ICEi).

Katie Gillies

Human - wd:Q43147907

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