Recipient organisationNIHR Leicester Biomedical Research Centre
NIHR supportRecorded as supported by this research centre
PeriodMar 2025 — Aug 2026
In plain English
AI plain-English summary
Around 250,000 people in the UK each year develop a build-up of fluid around the lung that leaves them breathless and unable to do everyday tasks. Draining the fluid with a semi-permanent tube called an indwelling pleural catheter (IPC) relieves symptoms, but the tube must be drained several times a week—usually by a community nurse. Patients or their carers can learn to do this themselves, a practice called self-management, which gives them more control and reduces demand on nursing services. Yet many who could self-manage do not get the chance. This project aims to change that. Researchers will interview patients, families, and healthcare professionals to identify what stops people from self-managing and what would help them start. They will then run co-design workshops to develop an intervention—a practical support package—that enables more patients to drain their own IPC at home. If successful, the intervention could give patients greater independence, improve their quality of life, and free up community nursing time for others who need it most.
View original technical description
A pleural effusion is a build-up of fluid around the lung. In the UK, about 250,000 people develop a pleural effusion each year. People with a pleural effusion feel breathless and can’t do the things they want to. Draining the fluid helps with this, reducing breathlessness and improving quality of life. This can be done by inserting a semi-permanent tube called an indwelling pleural catheter (IPC). This is drained at home several times a week, usually by a community nurse. However, it can be done by the patient or family/unpaid carer – this is called self-management. Self-management gives patients the freedom to drain their IPC when needed and reduces the use of community nursing services. Despite these benefits, not all patients get the opportunity to self-manage.The aim of this study is to help more patients self-manage if they want to. We will achieve this through three stages:Stage 1: We will talk to patients with IPC as well as their families/carers to find their views on self-management and what stops people who could self-manage from doing so. We know that patients with an IPC can be frail and their families/carers are often already doing a lot to support them. We will ask what might help them to self-manage.Stage 2: We will talk to healthcare professionals (HCPs) looking after patients with IPC to understand what they think about self-management. This will include community nurses and the hospital teams who put in IPCs.Stage 3: We will hold workshops with patients, their families/unpaid carers and HCPs to design an intervention that will help people to self-manage IPC. We will recruit mainly through clinical settings where IPCs are inserted (normally a hospital). The study will run for two years. Participants can take part in an interview, focus group and/or the co-design workshops.
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