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. 2010 Nov;197(5):350–356. doi: 10.1192/bjp.bp.109.074526

Early intervention services, cognitive–behavioural therapy and family intervention in early psychosis: systematic review

Victoria Bird 1,2,3,4,5,6, Preethi Premkumar 1,2,3,4,5,6, Tim Kendall 1,2,3,4,5,6, Craig Whittington 1,2,3,4,5,6, Jonathan Mitchell 1,2,3,4,5,6, Elizabeth Kuipers 1,2,3,4,5,6
PMCID: PMC2966501  PMID: 21037211

Abstract

Background

Early intervention services for psychosis aim to detect emergent symptoms, reduce the duration of untreated psychosis, and improve access to effective treatments.

Aims

To evaluate the effectiveness of early intervention services, cognitive–behavioural therapy (CBT) and family intervention in early psychosis.

Method

Systematic review and meta-analysis of randomised controlled trials of early intervention services, CBT and family intervention for people with early psychosis.

Results

Early intervention services reduced hospital admission, relapse rates and symptom severity, and improved access to and engagement with treatment. Used alone, family intervention reduced relapse and hospital admission rates, whereas CBT reduced the severity of symptoms with little impact on relapse or hospital admission.

Conclusions

For people with early psychosis, early intervention services appear to have clinically important benefits over standard care. Including CBT and family intervention within the service may contribute to improved outcomes in this critical period. The longer-term benefits of this approach and its component treatments for people with early and established psychosis need further research.

Early intervention services have been developed to address the needs of individuals with early psychosis. Typically, there is a delay between the onset of the first episode of psychosis and receiving an effective treatment – a period of untreated psychosis.1 Reducing this duration of untreated psychosis (DUP) for people with schizophrenia may lead to an improved prognosis.1–4 Early intervention services aim to detect emergent symptoms, reduce DUP, and improve early access to effective treatment, particularly in the ‘critical period’ (the first 3–5 years following onset).5–7 Although at the time there was little evidence for the effectiveness of this approach, early intervention services were developed in Australia, the USA, Canada, New Zealand and elsewhere; and the widespread deployment of such services was recommended in the National Service Framework for Mental Health8 and in the National Institute for Health and Clinical Excellence (NICE) guideline on schizophrenia for England and Wales.9

Since then, the provision of early intervention services has steadily increased,10 with 145 early intervention services currently operating in the UK, serving about 15 750 individuals (Care Services Improvement Partnership, personal communication, 2009). Early intervention teams have also gradually evolved and now often consist of community-based multidisciplinary mental health teams that provide a combination of pharmacotherapy, family intervention, cognitive–behavioural therapy (CBT), social skills training, problem-solving skills training, crisis management and case management.11,12 However, although the evidence base for early intervention services is growing, their specific benefits have not been clearly demonstrated.13,14 Therefore as part of an update of the NICE guideline on schizophrenia,9,15 we conducted a systematic review of early intervention services for people with a first or early episode of psychosis. Because early intervention services typically include an individually tailored combination of evidence-based psychological interventions, we also examined the data on the separate use of CBT and family intervention used specifically in the context of early psychosis.

Method

Search strategy and selection criteria

We identified randomised controlled trials (RCTs) of early intervention services, CBT or family intervention for people with early psychosis, using the original schizophrenia guideline9 and five bibliographic databases (CINAHL, CENTRAL, EMBASE, MEDLINE, PsycINFO). The database search was conducted in September 2009 and restricted to English language papers or papers with an abstract in English. Full details of the search strategy can be found in the online supplement. Additional papers were identified by searching the reference list of retrieved articles, tables of contents of relevant journals, recent systematic reviews and meta-analyses of interventions in schizophrenia, and suggestions made by members of the schizophrenia Guideline Development Group (a comprehensive review protocol can be found in the updated edition of the full schizophrenia guideline, available from www.nccmh.org.uk).15

Early psychosis was defined as a clinical diagnosis of psychosis within 5 years of the first psychotic episode or presentation to mental health services. Interventions addressing high-risk groups or ‘pre-psychotic’/prodromal populations were excluded, as were studies where the main focus of the intervention was not on psychosis or where the duration since the first psychotic episode was greater than 5 years.

Quality assessment

All trials meeting the eligibility criteria were assessed for methodological quality using a modified version of the SIGN checklist.16 Trials that were judged to be of adequate quality were included in the review. Trials that were not clearly described as randomised were excluded as were those with fewer than ten participants per intervention arm.

Data extraction

Two of the authors (V.B. and J.M.) entered study details into a database and assessed methodological quality. Three of the authors (V.B., C.W. and P.P.) extracted outcome data into Review Manager (RevMan version 5.0.18 for Windows XP; The Cochrane Collaboration, Oxford, UK). The assessment of study quality and all outcome data were double-checked by one author (C.W.) for accuracy, with disagreements resolved by discussion.

Where available, data were extracted for the following outcomes: hospital admission; psychotic relapse (if appropriate criteria were used); DUP; and mean positive and negative symptoms as measured using the Positive and Negative Syndrome Scale (PANSS),17 Brief Psychiatric Rating Scale (BPRS),18 Scale for the Assessment of Positive Symptoms (SAPS),19 and the Scale for the Assessment of Negative Symptoms (SANS).20 Outcome data were extracted at both end of treatment and follow-up (based on mean end-point scores). In light of the fundamental aims of early intervention services,12 data on remaining in contact with services and accessing psychosocial treatments were also extracted.

Statistical analysis

Meta-analysis was used, where appropriate, to synthesise the evidence using RevMan. Where possible, intention-to-treat with last observation carried forward data were used in the analyses. For binary outcomes, this approach assumes that participants leaving the study early, for whatever reason, had an unfavourable outcome. We calculated the standardised mean difference (SMD) for continuous outcomes, and relative risk (RR) for binary outcomes. For consistency, data from all outcomes (continuous and binary) were entered into RevMan in such a way that negative effect sizes or relative risks less than one favoured the active intervention. The number needed to treat for benefit (NNTB)21 was calculated for statistically significant relative risks. Data from more than one study were pooled using a random-effects model, regardless of heterogeneity between trials, as this has recently been shown to be the most appropriate model in most circumstances.22 Summary effects were assessed for clinical importance, taking into account both the point estimate and the associated 95% confidence interval (CI).

Results

The search process and total number of trials included in the review are illustrated in Fig. 1. Details of all included trials can be found in Table 1, with further information about included and excluded studies available in online Tables DS1 and DS2.

Fig. 1.

Fig. 1

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Flow diagram of selection of papers for inclusion in the clinical review.

CBT, cognitive–behavioural therapy; RCTs, randomised controlled trials. a. Includes RCTs published in multiple papers.

Table 1.

Characteristics of included trials

Study (primary paper) Total participants, n Treatment groups Duration and frequency of treatment Standard care comparison group Outcomes extracted for this review
Early intervention services
    COAST23 59 Early intervention service including psychological interventions as required 9 months follow-up reported, with service available 7 days a week including nights Local available CMHT services Leaving the study for any reason, PANSS not extracted as n < 10 in comparison arm at 9 months
    LEO11 144 Early intervention service established on principles of assertive outreach including psychosocial interventions 12 and 18 months follow-up reported, with extended hours service including weekends Local available CMHT services Leaving the study early, relapse, hospital admission, remaining in contact with services, receiving psychosocial interventions, positive symptoms (PANSS), negative symptoms (PANSS)
    OPUS24 547 Early intervention service: assertive community treatment, family intervention and social skills training 2-year treatment duration, with service available between 8am and 5pm with a crisis plan for each patient Services offered by local community mental health centres Leaving the study early, hospital admission, remaining in contact with services, positive symptoms (PANSS), negative symptoms (PANSS)
    OTP12
 50
Early intervention service: integrated treatment with structured psychological interventions
2-year treatment duration, with treatment session provided weekly – monthly over 2 years
Regular clinic-based services (80% from hospital out-patient, 20% local community general health services)
Leaving the study early, hospital admission, relapse receiving psychosocial interventions
Cognitive–behavioural therapy
    Jackson et al25 91 Individual CBT: cognitively oriented psychotherapy 40-minute session weekly or fortnightly for up to 12 months Early Psychosis Prevention and Intervention Centre (EPPIC) Positive symptoms (BPRS), negative symptoms (SANS), hospital admission
    Lecomte et al28 75 Group-based CBT tailored to first-episode psychosis 24 treatment sessions delivered twice a week for 3 months Local mental health clinic or early intervention programmes Positive symptoms (BPRS), negative symptoms (BPRS)
    Lewis et al26 203 Individual CBT: Study of Cognitive Reality Alignment Therapy in Early Schizophrenia 15–20 h within 5 weeks with booster sessions at a further 2 weeks, 1, 2 and 3 months Routine clinical care from local mental health units Positive symptoms (PANSS), negative symptoms (PANSS), relapse, hospital admission
    Wang et al27
 251
Individual CBT offered at recovery stage
Six weekly 40- to 50-minute sessions
Hospital services including clozapine or risperidone
Positive symptoms (PANSS), negative symptoms (PANSS), hospital admission
Family intervention
    Goldstein et al29 104 Family intervention: crisis oriented, individually delivered Six weekly intervention sessions Standard treatment with either low- or high-dose fluphenazine Relapse (end of treatment and 6-month follow-up)
    Leavey et al30 106 Family intervention: education and problem-solving Seven 1 h sessions Usual care from psychiatric services and CMHTs Hospital admission (end of treatment)
    Zhang et al31 78 Family intervention: group and individual sessions focused on education 18 months with contact every 1–3 months Standard hospital out-patient services Hospital admission (end of treatment)
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BPRS, Brief Psychiatric Rating Scale; CBT, cognitive–behavioural therapy; CMHT, community mental health team; COAST, Croydon Outreach and Assertive Support Team; LEO, Lambeth Early Onset team; OTP, Optimal Treatment Project; PANSS, Positive and Negative Syndrome Scale; SANS, Scale for the Assessment of Negative Symptoms.

Early intervention services

Four published trials (n = 800) were included in the meta-analysis of early intervention services: COAST (Croydon Outreach and Assertive Support Team);23 LEO (Lambeth Early Onset);11 the OPUS trial; 24 and OTP (Optimal Treatment Project).12 Inspection of the Cochrane review of early interventions in psychosis13 identified three additional trials; however, these were excluded as they failed to meet our inclusion criteria regarding the population studied and comparison used. All included trials recruited participants from local mental health services such as community mental health teams, in-patient and out-patient services. However, the trials varied as to whether the participant was a new referral, with LEO11 including only those making contact for the first or second time, whereas COAST,23 OPUS24 and OTP12 considered people who had a documented first contact within a specified time period, ranging from 12 weeks to 5 years. Interventions often included a case manager or care coordinator, with a lower case-load than in standard care. In addition to medication management, all participants allocated to early intervention services were offered a range of psychosocial interventions, including CBT,11,12,23 social skills training24 and family intervention12,23,24 or family counselling,11 and vocational strategies such as supported employment.11,12,23 The psychosocial and vocational interventions were usually adapted to the needs of first-episode psychosis and offered on an ‘as-required’ basis. The frequency and duration of contact differed between trials, with the duration of the intervention lasting up to 2 years. Outcomes were reported at 9 months to 5 years post-randomisation.

Participants receiving early intervention services, when compared with those receiving standard care, were less likely to relapse (35.2% v. 51.9%; NNTB for one extra patient to avoid relapse 6, 95% CI 3 to 25; heterogeneity I2 = 0%, P = 0.67) or be admitted to hospital (28.1% v. 42.1%; NNTB = 7, 95% CI 5 to 7; heterogeneity I2 = 0%, P = 1.00) (Table 2). Early intervention services also significantly reduced positive symptoms with a pooled SMD of –0.21 (95% CI –0.42 to –0.01; heterogeneity I2 = 9%, P = 0.29) and negative symptoms with a pooled SMD of –0.39 (95% CI –0.57 to –0.20; heterogeneity I2 = 0%, P = 0.38). The rate of discontinuation for any reason was lower for early intervention services compared with standard care (27.0% v. 40.5%; NNTB = 8, 95% CI 5 to 14; heterogeneity I2 = 40%, P = 0.17). In terms of access and engagement with treatment, although generally high, participants in early intervention services were more likely to remain in contact with the index mental health team (91.4% v. 84.2%; NNTB = 13, 95% CI 4 to); heterogeneity I2 = 0%, P = 0.79), and were twice as likely to receive a psychosocial intervention (36.6% v. 14.0%; NNTB = 5, 95% CI 4 to 6; heterogeneity I2 = 74%, P = 0.02).

Table 2.

Analysis of interventions for early psychosis compared with standard care (random-effects model)

Outcome Time of data collection Trials, n Participants, n: treatment/control Summary effect estimate (95% CI)
Early intervention service
    Hospital admission11,12,24 End of treatment 3 342/280 RR = 0.67 (0.54 to 0.83)
    Relapse (full or partial)11,12 End of treatment 2 91/81 RR = 0.66 (0.47 to 0.94)
    Positive symptoms (PANSS or SAPS)11,24 End of treatment 2 260/208 SMD = –0.21 (–0.42 to –0.01)
    Negative symptoms (PANSS or SANS)11,24 End of treatment 2 260/208 SMD = –0.39 (–0.57 to –0.20)
    Not receiving a psychological intervention11,12,24 End of treatment 3 344/286 RR = 0.67 (0.46 to 0.97)
    Not in contact with index team11,24 End of treatment 2 314/266 RR = 0.60 (0.39 to 0.92)
    Leaving the study early for any reason11,12,23,24
 End of treatment
4
408/392
RR = 0.71 (0.53 to 0.94)
Cognitive–behavioural therapy
    Positive symptoms (BRPS, PANSS or SAPS)25–28 End of treatment 4 285/251 SMD= –0.05 (–0.22 to 0.12)
    Positive symptoms26–28 Up to 2 years follow-up 3 233/209 SMD= –0.60 (–0.79 to –0.41)
    Negative symptoms (BRPS, PANSS or SAPS)25,27,28 End of treatment 3 207/191 SMD = 0.03 (–0.17 to 0.23)
    Negative symptoms26–28 Up to 2 years follow-up 3 233/209 SMD= –0.45 (–0.80 to –0.09)
    Relapse26,27 Up to 2 years follow-up 2 227/227 RR = 0.67 (0.24 to 1.85)
    Hospital admission25,26
 Up to 2 years follow-up
2
146/148
RR = 1.01 (0.76 to 1.35)
Family intervention
    Relapse29 End of treatment 1 52/52 RR = 0.58 (0.25 to 1.36)
    Relapse29 Up to 2 years follow-up 1 52/52 RR = 0.75 (0.39 to 1.43)
    Hospital admission30,31 End of treatment 2 99/90 RR = 0.51 (0.24 to 1.10)
    Hospital admission and relapse (combined)29–31 End of treatment 3 151/142 RR = 0.50 (0.32 to 0.80)
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BPRS, Brief Psychiatric Rating Scale; PANSS, Positive and Negative Syndrome Scale; RR, relative risk; SANS, Scale for the Assessment of Negative Symptoms; SAPS, Scale for the Assessment of Positive Symptoms; SMD, standardised mean difference.

Cognitive–behavioural therapy

Four published trials of CBT25–28 were included in the review (n = 620). One paper27 published in Chinese but with an English abstract was translated subsequent to publication of the schizophrenia (update) guideline15 and included in this analysis.

Participants were recruited from a range of services which included early intervention services, community mental health clinics and in-patient psychiatric wards. In two trials, participants were exclusively in their first episode of psychosis.25,27 Another trial26 additionally included participants who had been admitted for a second time, providing the episode occurred within 2 years of the first admission (17% of their sample). The fourth trial28 included participants who had consulted a mental health professional for psychosis for the first time in the past 2 years. Cognitive–behavioural therapy was delivered individually in three out of the four trials,25–27 with a group-based approach in the fourth.28 Two of the interventions specifically adapted the CBT approach for early psychosis,25,28 with the remaining two interventions targeting positive symptoms26 and insight building.27 The frequency of sessions and the duration of treatment varied across trials, with the total duration ranging from 5 weeks (plus booster sessions)26 to 1 year.25

At up to 2 years post-treatment follow-up, when compared with standard care alone, CBT significantly reduced mean positive symptoms with a pooled SMD of –0.60 (95% CI –0.79 to –0.41; heterogeneity I2 =0%, P = 0.44) and mean negative symptoms with a pooled SMD of –0.45 (95% CI –0.80 to –0.09; heterogeneity I2 = 62%, P = 0.07). These benefits were not evident at the end of treatment in terms of both positive (SMD = –0.05, 95% CI –0.22 to 0.12; heterogeneity I2 = 0%, P = 0.92) and negative symptoms (SMD = 0.03, 95% CI –0.17 to 0.23; heterogeneity I2 = 0%, P = 0.41), or relapse within the 2-year follow-up period (27.8% v. 32.2%, P= 0.44; heterogeneity I = 79%, P = 0.03). Rates of hospital admission up to 2 years follow-up also failed to demonstrate any additional benefit for CBT compared with standard care (38.4% v. 38.5%, P= 0.94; heterogeneity I2 = 0%, P = 0.36).

Family intervention

Three trials (n = 288) assessing family intervention in early psychosis were included in the review.29–31 Participants were recruited from psychiatric services, including in-patient units, and were either first or second admissions,29,31 or had made first contact with services within the past 6 months.30 Two trials29,30 included the individual with psychosis in the family sessions, whereas in Zhang et al31 the majority of family sessions did not include the patient. The interventions delivered in each trial included an element of psychoeducation and problem-solving, with crisis management also evident in one trial.29 Interventions varied in their mode of delivering, with two trials29,30 utilising an individual family approach and the remaining trial combining individual and group-based family sessions. Only one trial29 reported relapse and a further two trials30,31 reported hospital admission; these outcomes were combined to increase statistical power.

The combined analysis indicated that at the end of treatment, participants receiving family intervention were less likely to relapse or be admitted to hospital compared with those receiving standard care (14.5% v. 28.9%; NNTB = 7, 95% CI 4 to 20; heterogeneity I2 = 0%, P = 0.40). At up to 2 years follow-up, one study29 reported a numerically lower risk of relapse (23.1% v. 30.8%, P = 0.38), although this was not statistically significant. None of the included family intervention trials provided data on mean positive and negative symptoms.

Discussion

Main findings

For people with early psychosis, in four trials of early intervention services, four trials of CBT, and three trials of family intervention, meta-analysis demonstrated advantages over standard care. By the end of treatment, early intervention services produced clinically important reductions in the risk of both relapse and hospital admission. In addition, small effects favouring early intervention services were shown in terms of reduced symptom severity and improved access to and engagement with treatment (including psychological therapies). Family intervention also produced clinically important reductions in the risk of relapse and hospital admission when compared with standard care. In the 2 years following the intervention, medium effects favouring CBT were demonstrated in terms of reduced positive and negative symptom severity. We found no data on the effect of family intervention on symptoms and insufficient evidence to reach a conclusion about the impact of CBT on relapse or hospital admission.

Early intervention services

Compared with a previous review of early interventions in psychosis,13 our meta-analysis found stronger evidence to support the effectiveness of early intervention services overall. The earlier review included fewer trials that specifically focused on service-level interventions delivered during the ‘critical period’ following onset of psychosis. Furthermore, although the previous review included both discrete psychosocial and multicomponent service-level interventions, there was a lack of comparable trials for any conclusions to be drawn. Our findings do, however, substantiate those previously reported in a narrative review of randomised and non-randomised studies by Penn and colleagues,14 who concluded that early interventions had beneficial effects across a range of domains, although further investigation was needed to establish the robustness of these findings.14 Our review attempts to overcome these limitations and provides the first meta-analytic evidence indicating that both early intervention services and discrete psychological interventions improve outcomes for early psychosis.

In the present review, the early intervention services provided in all of the trials included the provision of psychosocial interventions, pharmacological treatment and some form of case management involving smaller case-loads (1:10) and an assertive approach to treatment. All of the components were tailored to meet the needs of the individual patient and offered at the earliest opportunity. These elements were not present in treatment as usual, although an assertive approach to treatment is so common that it cannot be specifically excluded. The psychological interventions used in the included trials were CBT and either family intervention12,23,24 or family counselling.11 It is possible that the reduced case-loads and more appropriate use of pharmacological interventions within early intervention services may account for some of the clinical and statistically important improvements demonstrated. Although further research is needed to investigate the beneficial contributions of these features of early intervention, given the positive effects of CBT and family intervention when delivered as discrete interventions for people with early psychosis, it is just as likely that these two psychosocial interventions have contributed to some of the benefits of early intervention services in this review.

Gleeson and colleagues32 recently demonstrated that the addition of a cognitive–behavioural and family therapy-based relapse prevention programme to an early intervention service for individuals in remission from a first episode of psychosis was more likely to prevent or significantly delay a second episode when compared with an early intervention service alone. In this trial the early intervention service alone included only family psychoeducation and peer support. This study provides some evidence to support our hypothesis: that an important part of the overall effectiveness of the early intervention teams included in our meta-analysis derives from the inclusion of two evidence-based psychological interventions, namely, CBT and family intervention. In our review we have shown that the likelihood of a service user receiving a psychosocial intervention in an early intervention team is double that found in a community mental health team.

Limitations

One limitation of the present review is the paucity of trials included in each meta-analysis. We excluded trials focusing on high-risk groups or prevention of psychosis because of the possible ethical implications of targeting interventions at these individuals.5 Another limitation is the variability in long-term follow-up measures available in different trials making some comparisons difficult. Only one trial of an early intervention service provided long-term data (up to 5 years post-randomisation),24 whereas all four trials of CBT25–28 and one of family intervention29 included long-term follow-up measures. Therefore, it remains to be determined whether the effects of early intervention services are sustained.

Psychological interventions

Despite the limitations, our findings regarding the efficacy of CBT and family intervention are consistent with, and reflect, the wider evidence base found in the treatment and management of later psychotic episodes. The updated edition of the schizophrenia guideline15 recommends that both interventions should be offered to people experiencing an acute episode of schizophrenia and for promoting recovery in those with established schizophrenia.

The evidence presented here suggests that CBT for early psychosis has longer-term benefits in terms of reducing symptom severity. Consistent with the wider evidence base for CBT for established psychosis, the present review failed to find any evidence that CBT reduced relapse rates in early psychosis, which suggests that the main benefits of this intervention are likely to be a reduction in symptoms and distress in early and established psychosis. This finding confirms a recent review assessing both RCTs and non-randomised studies of CBT in first-episode psychosis, which also failed to demonstrate positive effects on relapse and readmission.33

Although the number of RCTs for family interventions for early psychosis was limited in our review, the evidence is consistent with the larger body of evidence for the role of family interventions in established schizophrenia, in that family intervention reduced combined hospital admission and relapse rates. The review conducted for the updated edition of the schizophrenia guideline15 also found robust evidence for the efficacy of family intervention in established schizophrenia in reducing symptoms at the end of treatment. However, in the present review, none of the included trials reported measures that allowed us to assess this in the context of early psychosis. It is, therefore, anticipated that family intervention in first-episode psychosis may also reduce symptom levels.

Critical period

The studies included in the present review did not provide any data relating to DUP, as all papers focused on people with an agreed diagnosis, not on populations at high risk of becoming psychotic and receiving a diagnosis. A number of other reviews assessing DUP as a predictor have indicated that longer DUP is subsequently associated with poorer outcomes, including reduced adherence to CBT,34 altered response to antipsychotic medications,35 poorer social functioning36 and increased levels of disability.37 There is some suggestion from studies assessing the impact of early intervention programmes on high-risk and ultra-high-risk populations that education and awareness of psychosis may significantly reduce DUP.38 However, further research is needed to clarify issues surrounding DUP.39

The present review focused on the first 3–5 years following the onset of illness. This period has been defined as a critical period, when many of the psychological, clinical and social deteriorations associated with psychosis might occur,5,7,40 and when interventions might potentially have their greatest positive impact on prognosis.5,6 Although the current evidence to support this idea is limited, intervening at the earliest possible opportunity makes both practical and ethical sense, and hope remains that such intervention might reduce subsequent symptom severity, loss of functioning and other negative consequences of psychosis such as social exclusion.41 Intervening early may also help to reduce the adverse social and societal consequences of the disorder for both individuals and their family and carers. However, it can also be argued that providing excellent care and access to a range of appropriate and effective psychological, pharmacological and vocational interventions should be available at any stage of psychosis.42,43

Implications

On balance, the evidence reviewed here suggests that early intervention services are an effective way of delivering care for people with early psychosis and can reduce hospital admission, relapse rates and symptom severity, while improving access to and engagement with a range of treatments. The characteristics of these early intervention services include the provision of multigmodal psychosocial interventions, pharmacotherapy, and some form of case management with lower case-loads and an assertive approach to treatment, all within the context of intervening as early as possible. Our review also suggests that providing evidence-based psychological interventions as part of a comprehensive early intervention service may contribute to improving outcomes for people with early psychosis. It is important that these psychological interventions have been shown rather more robustly to be effective for people with established schizophrenia. This raises the possibility that comprehensive services comparable to those described here as early intervention services, which include a full range of evidence-based psychological interventions, should be considered for people with established psychosis.

Funding

T.K. receives, as director of the National Collaborating Centre for Mental Health (NCCMH), approximately £1.44 million per year from NICE to develop clinical guidelines. T.K. and C.W. were paid by the NCCMH to undertake the development of both the original and updated edition of the schizophrenia guideline. V.B. and I.M. were paid by the NCCMH to undertake the development of the updated edition of the schizophrenia guideline. T.K. was chair of the original NICE schizophrenia guideline and E.K. was chair of the updated edition. P.P. is supported by a Wellcome Trust Senior Research Fellowship to Veena Kumari (067427/z/02/z). The Biomedical Research Centre for Mental Health at the Institute of Psychiatry, King’s College London and the South London and Maudsley NHS Foundation Trust funds some clinical sessions for E.K.

Acknowledgments

We thank other members of the Guideline Development Group of the updated edition of the schizophrenia guideline and Ms Sarah Stockton for creating the search strategies and conducting the database searches. We also thank Dr Adegboyega Sapara for independently extracting the data for the CBT section of the review.

Declaration of interest

None.

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