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Randomized Controlled Trial
. 2025 Apr 7;15(4):e087206.
doi: 10.1136/bmjopen-2024-087206.

Patient and healthcare professionals' perception of weekly prophylactic catheter washout in adults living with long-term catheters: qualitative study of the CATHETER II trial

Affiliations
Randomized Controlled Trial

Patient and healthcare professionals' perception of weekly prophylactic catheter washout in adults living with long-term catheters: qualitative study of the CATHETER II trial

Sheela Tripathee et al. BMJ Open. .

Abstract

Objectives: To explore trial participants' experience of long-term catheters (LTC), the acceptability of washout policies, their experience of the CATHETER II trial (a randomised controlled trial comparing the clinical effectiveness of various washout policies versus no washout policy in preventing catheter associated complications in adults living with long-term catheters) and their satisfaction with the outcomes. The objectives of the healthcare professionals (HCPs) focus group and interview were to explore their attitudes towards weekly prophylactic catheter washout, views on the provision of training and participants' ability to enact washout behaviours.

Methodology: A longitudinal qualitative study embedded within the CATHETER II randomised controlled trial, which included semi-structured interviews and focus groups with participants from multiple trial sites. Data were analysed using the Theoretical Framework of Acceptability and Theoretical Domains Framework. This UK community-based study included 50 (24 female, 26 male) CATHETER II trial participants, aged between 23 and 100 years, with LTC and able to self-manage the washout and study documentation either independently or with the help of a carer. Seven HCPs (five female, two male) also participated.

Results: The participants had positive attitudes towards weekly prophylactic saline or acidic catheter washouts and other trial elements, such as washout training, catheter calendar and monthly phone calls. Participants and HCPs found the 'ask' of the CATHETER II trial and the weekly self-administered prophylactic washout policies to be feasible. The participants reported that the catheter washout training provided during the trial enhanced their self-efficacy, skills and self-reported capability to carry out the washouts. Participants reported having positive outcomes from the weekly washout. These included reduced blockage, pain or infection, reduced need for HCP support and greater psychological reassurance. HCPs attested to the participants' understanding of and adherence to the weekly washouts and other elements of the trial.

Conclusions: This study shows acceptability, feasibility and self-reported fidelity of the CATHETER II trial on a behavioural level. Self-management for prophylactic catheter washouts is both feasible and, following training, achievable without any need for additional support.

Trial registration number: ISRCTN17116445.

Keywords: clinical trial; health services; qualitative research; self-management; urinary incontinences; urology.

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Conflict of interest statement

Competing interests: All authors have completed the ICMJE uniform disclosure form at http://www.icmje.org/disclosure-of-interest/ and declare support from the NIHR Health Technology Assessment Programme for the submitted work. MA-F declares B. Braun Medical donated the supply of washout solutions for use in the CATHETER II study. B. Braun Medical commented on the manuscript prior to submission and these comments were considered so long as they did not compromise the scientific nature or neutrality of the publication. MAF declares travel sponsorship and, on occasion, speaker’s fees from numerous national and international conferences and non-profit organisations as a guest speaker and/or expert surgeon. DC reports grants, other than CATHETER II, from NIHR. JHL reports consulting fees as a MRCGP examiner; honoraria and fees for Pulse Live/Virtual, North-East Fellowship scheme and RCGP/RPS-CPCS (pharmacists) lectures and teaching; travel expenses for BNFC formulary committee and RCGP examiners; roles in NE England faculty RCGP Co Durham CCG, NICE; stocks in GSK, Haleon, Hikma Pharm, Smith and Nephew, Unilever and other non-medical companies and interests as a locum GP and COVID-19 consultant. All other authors have no completing interest to declare. No other financial relationships with any organisations that might have an interest in the submitted work in the previous 3 years are declared by all the authors.

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