Exploring Attitudes towards a Randomised Controlled Trial of Venous access Devices – a Nested Pre-trial Qualitative Study

Author:

Ritchie Moira1,Kelly Linda J.2,Moss Jonathan3,Paul James4,Shaw Rebecca1

Affiliation:

1. Health Economics and Health Technology Assessment, Institute of Health and Wellbeing, University of Glasgow, Glasgow - UK

2. School of Health Nursing and Midwifery, University of the West of Scotland, Hamilton - Scotland

3. Department of Interventional Radiology, NHS Greater Glasgow and Clyde, Glasgow - UK

4. Cancer Research UK Clinical Trials Unit, Institute of Cancer Sciences, University of Glasgow, Glasgow - UK

Abstract

Purpose This pre-trial qualitative research study was carried out to explore patient and clinical staff attitudes to central venous access devices (CVADs). In addition, views about participation in a randomised controlled trial (RCT) were explored with the aim of maximising recruitment to an imminent RCT of three CVADs. Methods Three patient focus groups (each comprising three patients) and 23 interviews with clinical staff were conducted. Interviews and focus group discussions were digitally recorded, transcribed verbatim, anonymised, uploaded to the QSR NVivo10 qualitative software programme and thematically analysed. Results Analysis of focus group interviews revealed the added challenges that a CVAD poses to patients with cancer. Four key themes emerged: continuity of daily life, pain and discomfort, stigma (a mark of disgrace associated with certain conditions) and self-preservation. The findings show the impact of a CVAD on patients’ ability to manage their condition. Clinical staff interviews highlighted several potential barriers to recruitment; a lack of equipoise (genuine clinical uncertainty as to which intervention is the most beneficial), concerns about the logistics of device insertion and a perceived requirement for education and training. Conclusions This qualitative study raises awareness of key areas of concern to patients who need a CVAD for chemotherapy delivery. It was identified that there is a need for clearer patient information around CVADs. Additionally it allows investigators to identify barriers to recruitment in a timely manner in order to minimise the potential for conflict between the roles of carer and researcher and consequently, maximise recruitment to the RCT.

Publisher

SAGE Publications

Subject

Nephrology,Surgery

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3. Protocol 13PRT/7956: Cancer And Venous Access (CAVA): a randomised controlled trial with associated qualitative research of venous access devices for the delivery of long-term chemotherapy (ISCRTN No 44504648). The Lancet Protocol Reviews 13PRT-7956. http://www.thelancet.com/protocol-reviews/13PRT-7956

4. Increasing recruitment to randomised trials: a review of randomised controlled trials

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