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Enhancing communication, informed consent and recruitment in a paediatric urgent care surgical trial: a qualitative
Frances C Sherratt1, Lucy Beasant2, Esther M Crawley2
1Institute of Population Health Sciences, University of Liverpool, Room 223, Second Floor, Block B, Waterhouse Building, 1-5 Dover Street, Liverpool, L3 5DA, UK.
Insights
Improving pediatric trial recruitment is key. Bespoke communication training enhanced informed consent and balanced trial arm presentation, increasing recruitment rates in the CONTRACT trial for appendicitis. Further strategies are needed to explore family preferences.
Area of Science:
- Pediatric clinical trials
- Surgical trial recruitment
- Health services research
Background:
- Paediatric trial recruitment in acute settings is challenging, particularly for trials comparing different management pathways.
- The CONservative TReatment of Appendicitis in Children (CONTRACT) trial aimed to improve recruitment and informed consent for appendicitis treatment options.
Purpose of the Study:
- To enhance informed consent and patient recruitment in the CONTRACT feasibility trial.
- To evaluate the impact of bespoke communication training on recruitment and informed consent processes.
Main Methods:
- A qualitative study embedded within the CONTRACT trial across three UK children's hospitals.
- Analysis of recruitment consultations and semi-structured interviews with health professionals and families.
- Bespoke communication training informed by ongoing qualitative analysis, focusing on balanced presentation of trial arms and managing expectations.
Main Results:
- Health professionals' presentation of trial arms became more balanced after training, leading to a recruitment rate increase from 38% to 62%.
- Professionals remained reluctant to explore family treatment preferences due to time constraints, coercion concerns, and child risk discussions.
- Families emphasized the need for clear explanations of trial timings and sensitive communication for recruitment and retention.
Conclusions:
- Bespoke communication training improved clarity and balance in presenting the CONTRACT trial, positively impacting recruitment rates.
- Despite training, challenges remain in exploring family preferences, highlighting the need for improved communication strategies in urgent care settings.
- Recommendations are provided to enhance communication, informed consent, recruitment, and retention in future paediatric trials in acute care environments.
Background:
Recruiting patients to paediatric trials can be challenging, especially in trials that compare markedly different management pathways and are conducted in acute settings. We aimed to enhance informed consent and recruitment in the CONTRACT trial (CONservative TReatment of Appendicitis in Children a randomised controlled Trial; ISRCTN15830435) - a feasibility trial that compared non-operative treatment (antibiotics) versus appendicectomy for uncomplicated acute appendicitis.
Methods:
Qualitative study embedded within CONTRACT and conducted across three UK children's hospitals. Data were transcribed audio-recordings of 85 CONTRACT recruitment consultations with 58 families; and semi-structured interviews with 35 health professionals and 28 families (34 parents, 14 children) invited to participate in CONTRACT. Data analysis drew on thematic approaches. Throughout CONTRACT, we used findings from the ongoing qualitative analysis to inform bespoke communication training for health professionals recruiting to CONTRACT. Before and after training we also examined qualitative changes in communication during consultations and quantitative changes in recruitment rates.
Results:
Bespoke communication training focussed on presenting the trial arms in a balanced way, emphasising clinical equipoise, exploring family treatment preferences and managing families' expectations about the trial's treatment pathways. Analysis of recruitment consultations indicated that health professionals' presentation of treatment arms became increasingly balanced following training, (e.g. avoiding imbalanced terminology) and recruitment rose from 38 to 62%. However, they remained reluctant to explore families' treatment preferences and respond with further information to balance these preferences. Analyses of interviews identified the time constraints of the urgent care setting, concerns about coercion, and reservations about exposing children to conversations about treatment risks as reasons for this reluctance. Interviews with families indicated the importance of clear explanations of trial treatment timings and sensitive communication of treatment allocation for both recruitment and retention.
Conclusions:
Following bespoke training based on the qualitative analyses, health professionals presented CONTRACT to families in clearer and more balanced ways and this was associated with an increase in the recruitment rate. Despite training, health professionals remained reluctant to explore families' treatment preferences. We provide several recommendations to enhance communication, informed consent, recruitment and retention in future trials in urgent care settings.
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