Introduction People with chronic epilepsy (PWE) often make costly but clinically unnecessary emergency department (ED) visits. Offering them and their carers a self-management intervention that improves confidence and ability to manage seizures may lead to fewer visits. As no such intervention currently exists, we describe a project to develop and pilot one. Methods and analysis To develop the intervention, an existing group-based seizure management course that has been offered by the Epilepsy Society within the voluntary sector to a broader audience will be adapted. Feedback from PWE, carers and representatives from the main groups caring for PWE will help refine the course so that it addresses the needs of ED attendees. Its behaviour change potential will also be optimised. A pilot randomised controlled trial will then be completed. 80 PWE aged ≥16 who have visited the ED in the prior 12 months on ≥2 occasions, along with one of their family members or friends, will be recruited from three NHS EDs. Dyads will be randomised to receive the intervention or treatment as usual alone. The proposed primary outcome is ED use in the 12 months following randomisation. For the pilot, this will be measured using routine hospital data. Secondary outcomes will be measured by patients and carers completing questionnaires 3, 6 and 12 months postrandomisation. Rates of recruitment, retention and unblinding will be calculated, along with the ED event rate in the control group and an estimate of the intervention's effect on the outcome measures. Ethics and dissemination Ethical approval: NRES Committee North West—Liverpool East (Reference number 15/NW/0225). The project's findings will provide robust evidence on the acceptability of seizure management training and on the optimal design of a future definitive trial. The findings will be published in peer-reviewed journals and presented at conferences. Trial registration number ISRCTN13 871 327.
‘Seizure First Aid Training’ for people with epilepsy who attend emergency departments, and their family and friends: study protocol for intervention development and a pilot randomised controlled trial
A. Noble,Anthony G Marson,C. Tudur-Smith,Myfanwy Morgan,Dyfrig A. Hughes,Steve Goodacre,L. Ridsdale
Published 2015 in BMJ Open
ABSTRACT
PUBLICATION RECORD
- Publication year
2015
- Venue
BMJ Open
- Publication date
2015-07-01
- Fields of study
Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
CITATION MAP
EXTRACTION MAP
CLAIMS
CONCEPTS
- dyad
A paired participant unit consisting of a person with epilepsy and one family member or friend recruited and randomized together.
Aliases: patient-family pair, patient-carer pair
- emergency department use
Use of emergency department services by participants, including visit frequency over the follow-up period.
Aliases: ED use, ED visits
- pilot randomized controlled trial
A small randomized trial used to test the feasibility and preliminary effects of the intervention before a definitive study.
Aliases: pilot RCT, randomised controlled trial
- questionnaire follow-up
Questionnaire assessment of patient and carer outcomes at 3, 6, and 12 months after randomization.
Aliases: 3-, 6- and 12-month questionnaires
- routine hospital data
Hospital-record data used to measure emergency department use in the pilot study.
Aliases: hospital routine data
- seizure management course
An existing group-based course from the Epilepsy Society that is being adapted for people with epilepsy and their carers.
Aliases: group-based seizure management course
- self-management intervention
The seizure-focused training intervention being developed to help participants and carers manage seizures and related care needs.
Aliases: Seizure First Aid Training, seizure management training
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