The Super EDEN Project
The Super EDEN project
SUstaining Positive Engagement and Recovery – The next step after Early Intervention for Psychosis
The Super EDEN programme is a NIHR funded project which builds upon the DoH funded National EDEN Project. Super EDEN began in June 2010 and will continue to run until June 2015, following up all service users who consented to the original National EDEN project to provide the evidence base to develop the ‘next generation’ of early intervention in psychosis services (EIS). This will: ensure that the gains made during EIS are maintained once users are discharged; enable the development of a ‘stepped care’ model of EIS to improve targeting of interventions appropriate to the emerging needs, illness trajectories and user preference; and evaluate a new intervention to improve structured activity levels in those who show a poor recovery from the first psychotic episode.
The Super EDEN project encompasses 3 studies:
Study |
Type |
Objectives |
Sample |
Study 1Maximising the impact, cost effectiveness and user experience of EIS |
Quantitative |
|
All those who consented to the National EDEN study (total n=1027) |
Study 2Perspectives in transition: A qualitative investigation of user, carer and staff views |
Qualitative |
|
Service users who are a part of study 1; 80 SU’s and 80 Carers who are nearing the end of their 2nd year in EIS. Focus groups at each of the EIS sites (year 2) and focus groups in primary care, CMHT’s and AOT’s (in years 2 and 3). |
Study 3Improving social recovery in young people with emerging severe social disability: A proof of principle randomised control trial |
RCT |
|
150 people with non-affective psychosis who are a) EIS clients b) show low level of structured activity after at least 1 year of treatment. Clients will be recruited between 1 and 2 years after entering EIS. Any clients who were a part of the original National EDEN study will be excluded. Recruitment will take place in 3 centres – B’ham, Norwich and Lancashire. Participants who are allocated to the treatment group in Birmingham will also be invited to participate in fMRI scanning (n=25) |
Summary MRI add-on study
Embedded within the trial, a functional MRI study will hopefully provide new insights into the underlying mechanisms supporting successful intervention. The study will recruit entrants to the SRCBT arm of the trial, and conduct scans pre and post intervention, with the aim of both predicted those who respond well to the SRCBT, and whether any improvement in structured activity is associated with significant change. A resting state functional scan and a task-based functional scan that activates the social cognition network will be used to confirm the neural basis of successful treatment.