Non-affective psychosis Mental and Behavioural Disorders Schizophrenia, schizotypal and delusional disorders
Conditions
Interventions
Current Interventions as of 03/04/2019:
All participants will be randomised to one of 2 trial arms, to receive either intensive CRT or CRT in a group setting.
Both CRT interventions (intensive/group)
Sponsors
King's College London
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Current participant inclusion criteria as of 03/04/2019: 1. Attending an Early Intervention Service or any individual within 5 years of their first episode of psychosis. At least three months from the onset of the first episode of psychosis. 2. Aged between 16 and 45 years 3. Research diagnosis of non-affective psychosis, i.e. schizophrenia, schizo-affective or schizophreniform disorder; 4. Ability to give informed consent. Previous participant inclusion criteria (as of 15/01/2018) 1. Attending an Early Intervention Service for at least three months 2. Aged between 16 and 45 years 3. Research diagnosis of non-affective psychosis, i.e. schizophrenia, schizoaffective or schizophreniform disorder 4. Ability to give informed consent Previous participant inclusion criteria 1. Attending an Early Intervention Service for at least six months 2. Aged between 16 and 35 years 3. Research diagnosis of non-affective psychosis, i.e. schizophrenia, schizoaffective or schizophreniform disorder 4. Ability to give informed consent
Exclusion criteria
Exclusion criteria: Current participant exclusion criteria as of 03/04/2019: 1. Inability to communicate in English sufficiently to participate in cognitive testing 2. Underlying organic/neurological condition affecting cognition (e.g. traumatic brain injury, seizure disorder) 3. Co-morbid diagnosis of learning disability 4. A definitive diagnosis of bipolar disorder Previous participant exclusion criteria: 1. Inability to communicate in English sufficiently to participate in cognitive testing 2. Underlying organic/neurological condition affecting cognition(e.g. traumatic brain injury, seizure disorder) 3. Co-morbid diagnosis of learning disability
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Achievement of goals is measured using the Goal Attainment Scale at baseline, post-CRT and at 6 months follow up | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Total number of hours of structured activity per week is measured using The Time Use Survey at baseline, post-CRT and at 6 months follow up 2. Costs of health and social care use measured using The Client Service Receipt Inventory at baseline, post-CRT and at 6 months follow up 3. Quality-adjusted life years (QALYs) measured using the EQ-5D at baseline, post-CRT and at 6 months follow up 4. Self-esteem measured using the Rosenberg Self Esteem Scale at baseline, post-CRT and at 6 months follow up | — |
Countries
England, United Kingdom
Contacts
Public ContactEmese Csipke
Outcome results
None listed