Your browser doesn't support javascript.
loading
Enhancing practitioners' confidence in recruitment and consent in the EcLiPSE trial: a mixed-method evaluation of site training - a Paediatric Emergency Research in the United Kingdom and Ireland (PERUKI) study.
Woolfall, Kerry; Roper, Louise; Humphreys, Amy; Lyttle, Mark D; Messahel, Shrouk; Lee, Elizabeth; Noblet, Joanne; Iyer, Anand; Gamble, Carrol; Hickey, Helen; Rainford, Naomi; Appleton, Richard.
Afiliação
  • Woolfall K; Department of Health Service Research, Institute of Population Health and Society, University of Liverpool, Liverpool, UK. K.Woolfall@liverpool.ac.uk.
  • Roper L; Department of Health Service Research, Institute of Population Health and Society, University of Liverpool, Liverpool, UK.
  • Humphreys A; Clinical Trials Research Centre (CTRC) North West Hub for Trials Methodology, University of Liverpool, Liverpool, UK.
  • Lyttle MD; Emergency Department, Bristol Royal Hospital for Children, Bristol, UK.
  • Messahel S; Faculty of Health and Applied Sciences, University of the West of England, Bristol, UK.
  • Lee E; Emergency Department, Alder Hey Children's NHS Foundation Trust, Liverpool, UK.
  • Noblet J; Emergency Department, Alder Hey Children's NHS Foundation Trust, Liverpool, UK.
  • Iyer A; Emergency Department, Alder Hey Children's NHS Foundation Trust, Liverpool, UK.
  • Gamble C; Neurology Department Alder Hey Children's NHS Foundation Trust, Liverpool, UK.
  • Hickey H; Clinical Trials Research Centre (CTRC) North West Hub for Trials Methodology, University of Liverpool, Liverpool, UK.
  • Rainford N; Clinical Trials Research Centre (CTRC) North West Hub for Trials Methodology, University of Liverpool, Liverpool, UK.
  • Appleton R; Clinical Trials Research Centre (CTRC) North West Hub for Trials Methodology, University of Liverpool, Liverpool, UK.
Trials ; 20(1): 181, 2019 Mar 21.
Article em En | MEDLINE | ID: mdl-30898169
ABSTRACT

BACKGROUND:

EcLiPSE (Emergency treatment with Levetiracetam or Phenytoin in Status Epilepticus in children) is a randomised controlled trial (RCT) in the United Kingdom. Challenges to success include the need to immediately administer an intervention without informed consent and changes in staffing during trial conduct, mainly due to physician rotations. Using literature on parents' perspectives and research without prior consent (RWPC) guidance, we developed an interactive training package (including videos, simulation and question and answer sessions) and evaluated its dissemination and impact upon on practitioners' confidence in recruitment and consent.

METHODS:

Questionnaires were administered before and immediately after training followed by telephone interviews (mean 11 months later), focus groups (mean 14 months later) and an online questionnaire (8 months before trial closure).

RESULTS:

One hundred and twenty-five practitioners from 26/30 (87%) participating hospitals completed a questionnaire before and after training. We conducted 10 interviews and six focus groups (comprising 36 practitioners); 199 practitioners working in all recruiting hospitals completed the online questionnaire. Before training, practitioners were concerned about recruitment and consent. Confidence increased after training for explaining (all scale 0-5, 95% CIs above 0 and p values < 0.05) the study (66% improved mean score before 3.28 and after 4.52), randomisation (47% improvement, 3.86 to 4.63), RWPC (72% improvement, 2.98 to 4.39), and addressing parents' objections to randomisation (51% improvement, 3.37 to 4.25). Practitioners rated highly the content and clarity of the training, which was successfully disseminated. Some concerns about staff availability for training and consent discussions remained.

CONCLUSIONS:

Training improved practitioners' confidence in recruitment and RWPC. Our findings highlight the value of using parents' perspectives to inform training and to engage practitioners in trials that are at high risk of being too challenging to conduct.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenitoína / Estado Epiléptico / Seleção de Pacientes / Emergências / Levetiracetam / Consentimento Livre e Esclarecido Tipo de estudo: Clinical_trials / Guideline / Qualitative_research Limite: Humans Idioma: En Revista: Trials Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenitoína / Estado Epiléptico / Seleção de Pacientes / Emergências / Levetiracetam / Consentimento Livre e Esclarecido Tipo de estudo: Clinical_trials / Guideline / Qualitative_research Limite: Humans Idioma: En Revista: Trials Ano de publicação: 2019 Tipo de documento: Article