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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
Prof
Carolyn
Chew-Graham
c.a.chew-graham@keele.ac.uk
Prof
Carolyn
Chew-Graham
c.a.chew-graham@keele.ac.uk
Schizophrenia, schizotypal and delusional disorders
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An Early Intervention in Psychosis (EIP) service offers treatment in the community to people with a first episode of psychosis. Psychosis is a severe form of mental illness with hallucinations and delusions. EIP offers care that includes medication, talking therapies, education about psychosis, physical health advice, support for families, and regular contact. Research has shown that EIP is effective, that people prefer it to other forms of treatment.
EIP is meant to be offered for up to three years to every person eligible for care. After this time, people who are well are discharged to their GP, while those with ongoing needs are transferred to the care of a general community mental health team. People can become unwell at this time of change and might benefit from longer treatment with EIP. We also know that some people who are well could possibly have been discharged back to their GP earlier. We want to develop a more tailored approach based on the needs of each individual and understand the health, social, and cost-benefits of this approach.
This qualitative study is part of a larger programme of work. In this study, we will interview people treated by EIP services at the time of their discharge, carers, health care professionals and managers who commission care to understand why and how decisions about care are made. Interviews enable people to tell their stories which will provide the researcher insight into their experiences.
Our entire research will be overseen by a group of EIP service users and carers. This group, led by a service user and carer, will help us to make sure the research is explained clearly; help us create the questions that are important for our interviews; and help us develop, promote and share our research and findings.
Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.
The recruitment start and end dates are as follows:
Observational type: Qualitative;
You can take part if:
You may not be able to take part if:
Service Users Exclusion Lack of capacity to give consent Unable to understand consent procedure Risk - expressing suicidal ideation
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Prof
Carolyn
Chew-Graham
c.a.chew-graham@keele.ac.uk
Prof
Carolyn
Chew-Graham
c.a.chew-graham@keele.ac.uk
The study is sponsored by University of Keele and funded by NIHR Central Commissioning Facility (CCF) .
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
Read full details
for Trial ID: CPMS 53730
You can print or share the study information with your GP/healthcare provider or contact the research team directly.