Skip to main content

International rates of receipt of psychological therapy for psychosis and schizophrenia: systematic review and meta-analysis

Abstract

Background

International clinical practice guidelines commonly recommend the provision of psychological therapies for psychosis and schizophrenia as an adjunct to medication. However, access to recommended therapies in routine clinical practice is limited. The aim of this review was to synthesise the available data on the provision of recommended psychological therapies for psychosis and schizophrenia across international mental health systems.

Methods

Electronic databases (PsychINFO, Pubmed and EMBASE) were searched for audits, service evaluation projects, or surveys, which reported data on rates of offer or receipt of any recommended psychological therapy or therapeutic intervention as part of routine clinical care.

Results

Twenty-two eligible studies from 9 countries were identified (N participants = 79,407). The most commonly recommended therapies in national guidelines were Cognitive-Behavioural Therapy for Psychosis (CBTp) and Family Interventions (FI). The overall pooled prevalence of rate of receipt of CBTp was 24% [95% CI 0.15–0.32] based on 15 studies (N = 42,494), with a higher rate of receipt of therapy found when pooling data from Early Intervention services only (41% [95% CI 0.21–0.60], 6 studies, N = 11,068). The overall pooled prevalence of rate of receipt of FI was 30% [95% CI 0.22–0.37] based on 14 studies (N = 13,863).

Conclusions

Overall rates of receipt of recommended psychological therapies for psychosis were low across the 9 countries data were available for in this review. However, there were high rates of heterogeneity across studies, meaning that pooled estimates should be interpreted with caution. Sources of heterogeneity included different service settings (e.g. early intervention vs. non-early intervention services), and varying methods used to collect the data (e.g. audit of electronic health records vs. self-report etc.). There were no available data from the continents of South America, Asia, or Africa, meaning that a truly global picture of provision of psychological therapies for psychosis and schizophrenia is currently lacking.

Introduction

Schizophrenia-spectrum disorders are characterised by core symptoms of psychosis including delusions, hallucinations, and thought disorder [1]. Schizophrenia is one of the top 10 leading causes of disability worldwide [2]. It is characterised by high rates of relapse and symptoms which can often persist across the lifespan [3]. People with schizophrenia and psychosis may receive care in a variety of settings including acute psychiatric wards, rehabilitation settings, and community mental health teams. Due to the complexity of service users’ needs, care is usually provided by a multi-disciplinary team including psychiatrists, mental health nurses, occupational therapists, social workers, and psychologists.

Clinical guidelines are significant drivers of national health policies and commissioning of services across international mental health systems. A 2011 review of international schizophrenia guidelines [4] focused on 5 guidelines including those from Australia/New Zealand (RANZCP; Royal Australian and New Zealand College of Psychiatry), United States of America (APA; American Psychiatric Association & PORT; Patient Research Outcomes Team), Germany (DGPPN; German Society of Psychiatry, Psychotherapy and Nervous Diseases) and the United Kingdom (NICE; National Institute for Clinical and Health Excellence)). All of these guidelines recommended psychosocial interventions as an adjunct to medication. There were some minor differences between guidelines in terms of recommended psychological therapies, but the therapies which were universally recommended were Cognitive-Behavioural Therapy for Psychosis (CBTp) and/or Family Interventions (FI).

The inclusion of psychological therapies as routinely recommended treatments for schizophrenia reflects a significant policy shift away from a solely pharmacological treatment approach, given the evidence base for psychological therapies in reducing distress and impairment associated with symptoms, and promoting recovery e.g. [5, 6]. In contrast to medical interventions, data regarding the implementation of psychological interventions is limited. For example, in a Cochrane review examining the efficacy of guideline implementation strategies only 2 out of 6 studies included data relating to psychological interventions [7]. A major charity commission in the United Kingdom (UK) found that service users often experience high levels of dissatisfaction with their care within schizophrenia/psychosis pathways and frequently reported inadequate support for families and carers, and lack of access to recommended psychological therapies [8]. Further evidence for limited access to therapies comes from a systematic review which reported implementation rates of between 4 and 100% for CBTp and 0–53% for FI, based on 11 UK-based studies [9]. The large variation in reported implementation rates arose due to sampling differences, and different methods used for assessing implementation rates across studies. For example, some studies used approaches which would be more affected by response bias, such as self-selecting service users responding to a charity survey. Other studies relied on staff report of receipt of therapies, rather than more robust methods such as independent auditing of electronic health records.

Evidence from other countries indicates that inadequate implementation of clinical guidelines for the provision of psychological therapies is not a UK problem only. For example, a recent review of schizophrenia guidelines across 12 countries in South-East Europe (including Croatia, Greece, and Serbia) found that although most recommended psychological therapies including CBTp and FI, they were poorly implemented in routine care, often due to a lack of trained staff [10]. Comprehensive data on actual rates of receipt of therapy is not available for every country which has schizophrenia treatment guidelines. Some studies have used proxy measures to assess clinical guideline implementation such as availability of trained clinicians. A study using this approach estimated the accessibility of CBTp in the USA and Canada by using a national survey of workforce training and reference to known prevalence rates of schizophrenia [11]. The findings suggested that only 0.57% of the mental health workforce were CBTp trained, representing between 11.5 and 22.8 CBTp trained clinicians per 10,000 people with a schizophrenia/psychosis disorder. Based on this, the authors concluded that recommended psychological therapies remain largely inaccessible to service users in North America.

In summary, psychological therapies for psychosis are now routinely recommended in international clinical guidelines, but service users may not be able to access these therapies due to low rates of implementation in routine clinical practice. The only previous systematic review on implementation of clinical guidelines for psychological therapies for schizophrenia/psychosis was based on UK studies only [9], meaning that a global picture of implementation is lacking. The current review aimed to fill that gap by searching for and synthesising available international data on implementation of evidence-based psychological therapies for schizophrenia/psychosis. This addresses a question of high importance to service users and carers, alongside mental health clinicians and healthcare commissioners, in terms of ensuring fair access to evidence-based therapies.

Method

Review question

What are international rates of receipt of nationally recommended psychological therapy for psychosis?

Registration of review protocol

We wrote a review protocol and registered it on the Open Science Framework (https://doi.org/10.17605/OSF.IO/FSEQM; date uploaded 2nd December 2020) and the online Prospero database (https://www.crd.york.ac.uk/PROSPERO; CRD42020224002; date registered 14th December 2020). This review is reported in line with Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines [12].

Searches

We searched for relevant peer reviewed journal articles in electronic databases (PsychINFO, Pubmed and EMBASE) published from 1st January 2010 up until 27th November 2020 (the date the initial searches were run). The searches were then updated on 21st November 2022. The rationale for this time frame was to give a comprehensive picture as possible of current practice, whilst also allowing for the effect of updating of recommendations in line with new research evidence accumulating over time. See Additional file 1 for a complete list of search terms. We were already aware of two government reports related to UK data therefore a basic internet search using comparable search terms was conducted in an attempt to identify corresponding reports for different countries (‘Identification of new studies via other methods’ in PRISMA diagram).

Inclusion/exclusion criteria

Study design

Audits, service evaluation projects, surveys.

Setting

Any adult (18+) mental health team or service, or early intervention service open to both under and over 18s.

Language

Any (Google translate was used where necessary to assess eligibility for papers published in languages other than English).

Participants

Adults (> 18 years) with any psychosis spectrum disorder as defined by the 10th revision of the International Statistical Classification of Diseases and Related Health Problems (ICD-10) codes (F20-29) [13] or any schizophrenia spectrum disorder as defined by the Diagnostic and Statistical Manual of Mental Health Disorders 5th edition (DSM-5), or previous versions of these diagnostic manuals where relevant [14]. Studies involving participants with a mixed age range including some < 18 years were also included.

Intervention

Studies reporting observed rates of offer, referral, or receipt of any recommended psychological therapy or therapeutic intervention delivered as part of routine clinical care or service evaluation project (i.e. not as part of a clinical trial, or other study involving randomisation to condition). We referred to relevant national guidelines to help determine whether the inclusion criteria of being ‘recommended’ (in the country where the study was conducted) was met (e.g. National Institute for Health and Care Excellence (NICE) guidelines for UK based studies). Studies relating to countries where national guidelines on recommended therapies were not available were included where they reported on interventions which were present in other guidelines.

Outcomes

Papers reporting proportions of service users being offered and/or receiving recommended psychological interventions.

Study selection and data extraction

All studies were independently double screened by two reviewers at both title/abstract and full-text stage using the systematic review software Covidence (https://www.covidence.org/). Any discrepancies were resolved by discussion to reach consensus, with consultation with the senior author where needed to reach a final decision. We contacted corresponding authors to ask for additional information needed to assess eligibility where necessary. For summary of searches see PRISMA diagram (Fig. 1). We extracted data on the number of service users being offered and/or receiving recommended psychological interventions (numerator), and the size of the total sample (denominator) in order to calculate a pooled estimate of proportions across studies. We also extracted data where available on potential predictor variables of therapy receipt including age, ethnicity, diagnosis, gender, marital status, and service type. All data was independently double extracted by two reviewers using a standardised template.

Fig. 1
figure 1

PRISMA Diagram

Quality assessment

A modified version of the Joanna Briggs Institute Critical Appraisal Checklists for Studies Reporting Prevalence data was used to assess the quality of studies [15] as recommended for this type of review [16]. For the purposes of this review, we removed Question 3 (Was the sample size adequate?) as this was difficult to apply to routine clinical settings where the sample size was predetermined due to the size of the service being audited. The tool was further modified to include a scoring system to facilitate the comparison of studies. Studies were scored as follows on the 8 remaining questions: Yes = 2, No = 1, Unclear = 0. Final scores were then presented as percentages (with the denominator adjusted where relevant if any questions were assessed as not relevant to a particular study). Quality assessment was single-rated, with a random sample (6/22; 27%) double-checked by the senior author for accuracy.

Data analysis

The proportion of service users being offered or receiving a recommended therapy was calculated using the following formula:-

$$\left(\frac{\mathrm{People \,who \,received \,recommended \,psychological \,therapy }}{\mathrm{People \,in \,the \,service}/\mathrm{sample}}\right)*100$$

Analyses were performed separately for offer and receipt of therapy. A pooled estimate of proportions was calculated using a random effects model using the ‘Metaprop’ package in Stata [17]. This model ensures that the combined estimate captures the range of populations present across studies, rather than weighting studies solely by sample size, as individual studies regardless of size may contain information regarding a population that no other study has captured [18]. Pooled estimates were depicted graphically using a forest plot. Heterogeneity was examined using the I2 statistic. We aimed to run additional analyses on possible predictors of therapy receipt based on demographic or clinical characteristics (age, ethnicity, diagnosis, gender, marital status, and service type) where data were available. Sensitivity analyses were conducted by pooling prevalence rates from EI studies alone for both receipt of CBTp and FI as well as for studies referring to data from countries with defined treatment guidelines compared with countries where no treatment guidelines were available.

Results

Study selection

A total of 20,806 records were identified from database searches, and 12,646 were screened at title/abstract stage after duplicates were removed; 262 reports were identified as potentially eligible and sought for retrieval; 253 records were screened at full-text review plus an additional 2 records which were identified via other sources; a further 233 studies were excluded after this stage, with a total of 22 unique studies being identified as eligible for inclusion in the review. See Fig. 1 (PRISMA diagram) for a summary of how studies were selected.

Overview of study design and characteristics

See Table 1 for characteristics of the 22 included studies. Included studies came from 9 different countries, all from the continents of Europe, North America, or Australia (United Kingdom (n = 9), United States of America (n = 4), Canada (n = 3), Australia (n = 1), Ireland (n = 1), Portugal (n = 1), France (n = 1), The Netherlands (n = 1), Spain (n = 1)). Ten of the 22 studies were from Early Intervention teams with the remainder including a range of clinical settings including recovery teams, community mental health teams, public services, individuals following discharge from hospital, inpatient units, and outpatient clinics. Studies reported data mainly collected through audits of healthcare records or service user/staff surveys; however, many studies did not provide specific details of how data were collected. Sample sizes ranged between 35 and 35,812 people. Studies reported data for service users receiving Cognitive Behavioural Therapy for Psychosis (CBTp) (n = 16), Family Interventions (FI) (n = 14), Psychotherapy (n = 1) and Cognitive Remediation Therapy (n = 2). Most studies reported data from over a 12-month period (n = 15). Other time frames included 6 months (n = 1), 2 years (n = 1), 3 years (n = 4), 4 years (n = 1), 10 years (n = 1) and not specified (n = 1).

Table 1 Characteristics of included studies

Quality assessment

The overall quality of included studies was good, with the majority of studies (17/22) scoring above 75% (Table 2). The lowest scoring studies were Breitborde et al. [19] (63%) and Clarke et al. [20] (50%) largely due to issues regarding unclear methods of data collection and sampling.

Table 2 Quality assessment data

Quantitative synthesis of prevalence of offer/receipt of therapy: meta-analysis

Cognitive-behavioural therapy for psychosis (CBTp)

Three studies reported data for both proportions of service users being (i) offered and (ii) receiving (CBTp) within the same sample [21,22,23]. The distinction between offer and receipt is important, as not everyone who is offered therapy may be expected to take up the offer. Two studies reported low rates of both offer and receipt of CBTp in Community Mental Health Teams in the UK, with only a small gap between the prevalence rates for offer and receipt (11% vs. 6.3% respectively [22]; 6.9% vs. 5.3% [23]). In contrast, a study reporting data solely from Early Intervention teams (which provide care for people for a time-limited period of time after a first episode of psychosis) reported a similar rate of receipt of CBTp (6.5%) but a much higher rate of offer of CBTp (67.7%) [21]. One additional study reported data solely on offer of CBTp [24] but not receipt, whilst 12 studies reported data solely on receipt of CBTp, but not offer [19, 20, 25,26,27,28,29,30,31,32,33,34]. This perhaps reflects the added difficulties in assessing whether someone has been offered therapy, as this may not be formally recorded in the same way as attendance at therapy sessions etc. which can be more easily audited through clinical notes.

For all the studies which reported data on service users being offered CBTp (k = 4, n = 7006) a random effects model yielded a pooled prevalence rate of 23% (95% CI 0.11–0.35). See Additional file 2: Fig. S1) for forest plot. The pooled prevalence rate for service users receiving CBTp (k = 15, n = 42,494) was 24% (95% CI 0.15–0.32; see Fig. 2). Heterogeneity was high in both models (I^2 = 98.4% & 99.8% respectively). We ran a sensitivity analysis to compare the prevalence rate for studies where guidelines were clearly defined (k = 13, n = 42,272) with the rate for the two studies where no treatment guidelines were found [30, 32], (k = 2, n = 222). The random effects model showed a prevalence rate of 22% (95% CI 0.13–0.30) and 20% (95% CI 0.15–0.25) respectively, which were both comparable to the pooled prevalence rate for all 15 studies together (24%). See Additional file 2: Figs. S2 and S3 for forest plots).

Fig. 2
figure 2

Pooled prevalence of service-users who received Cognitive Behavioural Therapy for psychosis (CBTp)

We observed that studies reporting data from Early Intervention (EI) settings appeared to show higher rates of therapy receipt compared to non-EI settings. We ran a sensitivity analysis by pooling prevalence rates from EI studies alone reporting data on receipt of CBTp (k = 6, n = 11, 068). The random effects model showed a pooled prevalence rate of 41% (95% CI 0.21–0.60), which was higher than the pooled prevalence rates for all studies combined (24%) indicating that on average rates of receipt are higher in EI compared to non-EI settings (see Additional file 2: Fig. S4 for forest plot).

Family intervention (FI)

Only two studies reported prevalence rates of service users being offered FI. These were Rathod et al. [21] who reported a rate of 64.5% (80/124 service users) and Haddock et al. [23] who reported a rate of 1.6% (3/187 service users). As noted earlier, this large difference in rates is likely to reflect differences in the clinical setting, with Rathod et al. reporting data from an Early Intervention service and Haddock et al. reporting data from general Community Mental Health Teams. Fourteen studies reported prevalence rates of service users receiving FI (n = 13,863). The random effects model showed a pooled prevalence rate of 30% (95% CI 0.22–0.37; see Fig. 3). Heterogeneity was very high (I^2 = 99.4%).

Fig. 3
figure 3

Pooled prevalence of service-users who received Family Intervention (FI)

We similarly ran a sensitivity analysis on studies reporting data on receipt of Family Interventions (FI) from Early intervention (EI) settings only (k = 8, n = 11,476). The random effects model yielded a pooled prevalence rate of 32% (95% CI 0.20–0.44), which was the same as for the pooled prevalence rate for all 14 studies together including both EI and non-EI services (30%). See Additional file 2: Fig. S5) for forest plot.

Other recommended therapies

Five studies [19, 33, 35, 36] reported rates of receipt of other recommended therapies including metacognitive remediation therapy, psychotherapy, and cognitive remediation therapy (see Additional file 2: Table S1 for summary).

Narrative synthesis of predictors of offer/receipt of therapy

Data was extracted where available for predictors of therapy receipt. Due to significant differences across studies in how data were collected and reported (for example, different categorisation of age brackets) it was not possible to statistically pool results across studies in a meaningful way. We focused therefore on a narrative synthesis of these findings (see Additional file 2: Table S2 for summary).

Age was investigated as a possible predictor of the receipt of therapy by five studies, with four of these studies reporting data relating to receipt of CBTp [23, 28, 29, 32, 34] and one relating to Family Interventions [37]. Colling et al. [29] reported a statistically significant effect of age on receipt of therapy (CBTp), reporting that in their sample, under 41s were more likely to have received CBTp than over 41s (odds ratio (OR) = 1.57; 95% CI 1.01–1.72). Mason et al. [34] reported a Welch two sample t-test which found significant between-group differences in age (t = 15.34, p < 0.01), where those who had received CBTp had a lower mean age (M = 33.12 SD = 11.5) compared with those who did not (M = 35.88, SD = 13.08). Harvey et al. [28] reported that females in their study (conducted in Australia) were more than twice as likely to receive CBTp than males (OR = 2.21; 95% CI 1.60–3.05). However, three UK studies reported no statistically significant effect of gender on likelihood of therapy receipt [23, 29, 34]. Two of these UK studies also reported data on ethnicity as a possible predictor of receipt of CBTp. Haddock et al. reported no statistically significant effect, whereas Colling et al. reported that White service users were more likely to receive CBTp compared to Black service users (OR = 1.43; 95% CI 1.10–1.85). A USA study reported no statistically significant effect of ethnicity on likelihood of receipt of Family Interventions in an Early Intervention setting [37].

Four studies reported diagnosis as a significant predictor of therapy receipt. Harvey et al. [28] reported that service users with non-affective psychosis were more likely to receive CBTp compared to service users with affective psychosis (OR = 2.51; 95% CI 1.79–3.52). Haddock et al. [23] reported that service users with a diagnosis of ‘other psychosis’ were more likely to receive CBTp compared to schizophrenia (OR = 3.75), with Colling et al. [29] reporting similar findings. Mason et al. [34] reported significant effects of having a comorbid diagnosis of depression (χ2 = 87.36), bipolar (χ2 = 71.94) or anxiety (χ2 = 118.28). Colling et al. [29] also reported service type as being a significant predictor of therapy receipt with service users in Early Intervention (EI) teams more likely to receive CBTp than service users in non-EI teams (OR = 1.98; 95% CI 1.40–2.81).

Discussion

This systematic review and meta-analysis aimed to synthesise the available data on international rates of receipt of recommended psychological therapies for psychosis in routine clinical practice. We also aimed to summarise the available evidence on predictors of receipt of psychological therapy such as service type, age, and ethnicity. We found data from 9 different countries within 3 continents (Europe, North America, Australia), with many eligible studies being from the UK (9/22). All were high income countries according to World Bank classifications. Overall, this indicates a lack of available data from low- and middle-income countries, and from high-income countries outside of the UK, and especially from the continents of South America, Africa, and Asia which were not represented in our sample at all.

Overall, our results indicate low rates of both offer and receipt of recommended therapies (CBTp offered = 23% [95% CI 0.11–0.35], CBTp received = 24% [95% CI 0.15–0.32], FI received = 30% [95% CI 0.22–0.37]). When data was pooled from Early Intervention (EI) services only, rates of CBTp receipt was found to be higher (41% [95% CI 0.21–0.60]) but similar for FI (32% [95% CI 0.20–0.44]). It is important however to note the high level of heterogeneity between studies, which means that pooled estimates should be interpreted with caution. Only 5/22 studies reported any data on clinical and demographic characteristics which might be predictors of likelihood of therapy receipt. These data could not be meaningfully combined in a quantitative synthesis due to differences in how factors were defined and how data were reported between studies. A narrative synthesis indicated no consistent findings on the effect of age, gender, ethnicity, diagnosis, or marital status on therapy receipt. Colling et al. [29] and Mason et al. [34] both reported significant effects of age indicating that younger people were more likely to receive therapy than older people; this is likely due to the fact that receipt of therapy was more common in EI services than non-EI, and EI service users are usually younger due to the onset of a first episode commonly occurring in late adolescence/early adulthood.

Despite psychological therapies being recommended as evidence-based interventions alongside medication in international clinical guidelines, their availability lags far behind medication according to the findings of this review. Medication is almost always available to people with a diagnosis of schizophrenia, although discontinuation rates are high [38]. In contrast the current data indicates only around a third of service users receive internationally recommended therapies (CBTp and FI), with high levels of variation both within and between countries. The absence of clearly defined treatment guidelines did not appear to influence prevalence rates, however due to the small number of studies where this was the case (n = 2), it is difficult to draw any substantial conclusions. The results of this review are broadly consistent with the findings of the previous review by Ince et al. [9] which was focused on UK-based studies only, and reported rates of receipt of CBTp from 4 to 100%. The wide range of different rates of therapy receipt in both the current and the Ince review likely arose due to similar factors such as differences between studies in the criteria used to determine offer or receipt of therapy and differing methods of data collection.

Our findings indicated higher levels of implementation of CBTp in Early Intervention (EI) services compared to all service types pooled together. This may reflect policies in some countries which aim to optimise the care people receive when they experience a first episode of psychosis, to maximise the chance of a good recovery and to preserve personal, social, and occupational functioning as much as possible. For example, in the UK National Health System (NHS) a new access and waiting time standard for early intervention in psychosis services was introduced in 2016, meaning that at least 50% of people experiencing a first episode of psychosis must start treatment within 2 weeks of referral, and treatment must be in line with NICE (National Institute for Clinical and Health Excellence) guidelines. The Early Intervention model for first episode psychosis is becoming more widespread internationally, which may lead to increased access to psychological therapies for people in these services. For example the NAVIGATE program which was initially developed in the USA for people with first episode psychosis is now being rolled out in Israel [39]. However, despite the rapid proliferation of coordinated speciality care to improve outcomes for people experiencing a first episode of psychosis, access to psychological therapies for people outside of early intervention services may lag behind based on the findings of this review.

In order to improve access to recommended psychological therapies, it is important to understand barriers and facilitators to implementation. Previous reviews which have synthesised the available data on barriers to guideline implementation for CBTp and FI, have shown that barriers arose at multiple levels including organisational, staff, and service user levels [9, 40, 41]. These included negative staff attitudes towards referring service users for therapy, lack of specialised training available for staff to deliver the therapy, and dominance of a biological model of care [42]. Similar findings were reported from a study of staff attitudes, social norms, and behavioural control in Canada and Australia, with survey data suggesting that these staff factors significantly predicted CBTp delivery in practice [43].

In terms of strengths and limitations of this study, we followed best practice in the conduct of systematic reviews and meta-analyses according to Cochrane review standards. This included writing and pre-registering a comprehensive review protocol, keeping an audit trail of any subsequent protocol changes, and double-rating all records at both title/abstract and full-text stages. Our searches returned over 10,000 records indicating a comprehensive search; however relevant studies could have been missed given the complexities of writing effective search teams for such a broad topic. We did not search grey literature on the basis that the data we were looking for would most likely be found in the peer-reviewed literature, however this again may have led to relevant papers being missed. Our inclusion criteria specified studies which reported data on interventions included in treatment guidelines, however, it is possible that relevant data may have been missed where studies reported on therapeutic interventions that were not clearly defined and therefore not identifiable as ‘recommended’ e.g. [44, 45]. Prior to the study we were aware of government reports that gave relevant data in the UK, however, we were unable to find equivalent data in other countries which also could have been missed.

Although overall the methodological quality of the included studies was high, there was a wide range of methods and clinical settings included across studies, making a coherent synthesis more challenging. For example, some studies used more robust methods of assessing offer and receipt of therapy such as independent reviewing of electronic health records using key search terms e.g. Colling et al. [29]. Other studies used methods more open to response bias such as inviting service users with psychosis for interviews where not all eligible people took part [28]. There was also a considerable amount of variation across studies in terms of how interventions were defined with regards to therapy content, number of sessions, clinicians delivering intervention etc. The NICE guidelines in the UK for example recommend that CBTp be delivered over at least 16 sessions, but most studies used a much lower threshold for defining ‘receipt’ of therapy which could be attending only one or two sessions. We intentionally excluded data from randomised controlled trials as we wanted to focus on rates of receipt within routine clinical care. However, we included data from a range of other study designs, which added to the heterogeneity of the studies included in the review. This was largely a pragmatic decision, given that studies lie on a spectrum from observational to interventional, rather than these being discrete categories. Service evaluation projects which were further along the spectrum towards the interventional end were unsurprisingly more likely to report higher rates of receipt of therapy. For example, two of the studies reporting the highest rates of CBTp receipt (~ 60%) both reported outcomes from newly set up services for first episode psychosis which included universal access to recommended therapies as part of the care pathway [19, 30], which is not standard across other services.

For future research, there is a need for more data on recommended treatments and implementation of guidelines for schizophrenia and psychosis in middle- and lower-income countries, and from the continents of Asia, South America, and Africa. Mental health care systems differ widely across different countries in terms of how they are funded and delivered [46, 47]. A fully international view must of course take into account cultural, spiritual, and religious differences in how schizophrenia and psychosis are conceptualised in relation to causes, social stigma, and acceptability of psychiatric treatment [48].

Conclusion

The findings of this review indicate varying rates of receipt of recommended psychological therapies across 9 different countries; however, overall low rates of implementation indicate room for improvement in terms of increasing access to therapies in line with clinical guidelines. The available data were UK-centric, and there were no eligible studies found from the continents of South America, Asia, or Africa, meaning that a truly global picture of provision of psychological therapies for psychosis and schizophrenia is currently lacking.

Availability of data and materials

The datasets generated and/or analysed during the current study, and STATA analysis script, are available on the Open Science Framework repository, https://doi.org/10.17605/OSF.IO/FSEQM.

Abbreviations

APA:

American Psychiatric Association

CBTp:

Cognitive-Behavioural Therapy for Psychosis

DSM-5:

Diagnostic and Statistical Manual of Mental Health Disorders 5th edition

DGPPN:

German Society of Psychiatry, Psychotherapy and Nervous Diseases

EI:

Early Intervention

FI:

Family Intervention

ICD-10:

International Statistical Classification of Diseases and Related Health Problems

NHS:

National Health System

NICE:

National Institute for Clinical and Health Excellence

OR:

Odds ratio

PORT:

Patient Research Outcomes Team

PRISMA:

Preferred Reporting Items for Systematic Reviews and Meta-analyses

RANZCP:

Royal Australian and New Zealand College of Psychiatry

UK:

United Kingdom

USA:

United States of America

References

  1. World Health Organisation. International classification of diseases for mortality and morbidity statistics (11th Revision) 2018. https://icd.who.int/browse11/l-m/en#/http://id.who.int/icd/entity/1683919430.

  2. World Health Organisation. Global Burden of Disease: Disease incidence, prevalence and disability. 2004. https://www.who.int/healthinfo/global_burden_disease/GBD_report_2004update_part3.pdf.

  3. Schneider-Thoma J, Chalkou K, Dörries C, Bighelli I, Ceraso A, Huhn M, et al. Comparative efficacy and tolerability of 32 oral and long-acting injectable antipsychotics for the maintenance treatment of adults with schizophrenia: a systematic review and network meta-analysis. The Lancet. 2022;399(10327):824–36.

    Article  CAS  Google Scholar 

  4. Gaebel W, Riesbeck M, Wobrock T. Schizophrenia guidelines across the world: a selective review and comparison. Int Rev Psychiatry. 2011;23(4):379–87.

    Article  PubMed  Google Scholar 

  5. Lincoln TM, Peters E. A systematic review and discussion of symptom specific cognitive behavioural approaches to delusions and hallucinations. Schizophr Res. 2019;203:66–79.

    Article  PubMed  Google Scholar 

  6. Onwumere J, Bebbington P, Kuipers E. Family interventions in early psychosis: specificity and effectiveness. Epidemiol Psychiatric Sci. 2011;20(2):113–9.

    Article  CAS  Google Scholar 

  7. Bighelli I, Ostuzzi G, Girlanda F, Cipriani A, Becker T, Koesters M, et al. Implementation of treatment guidelines for specialist mental health care. Cochrane Database Syst Rev. 2016;12(12): Cd009780.

    PubMed  Google Scholar 

  8. Commission TS. The Abandonded Illness: A report by the Schizophrenia Commission. London; 2012.

  9. Ince P, Haddock G, Tai S. A systematic review of the implementation of recommended psychological interventions for schizophrenia: Rates, barriers, and improvement strategies. Psychol Psychother. 2016;89(3):324–50.

    Article  PubMed  Google Scholar 

  10. Stevović LI, Repišti S, Radojičić T, Sartorius N, Tomori S, Kulenović AD, et al. Non-pharmacological interventions for schizophrenia—analysis of treatment guidelines and implementation in 12 Southeast European countries. Schizophrenia. 2022;8(1):10.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Kopelovich SL, Nutting E, Blank J, Buckland HT, Spigner C. Preliminary point prevalence of Cognitive Behavioral Therapy for psychosis (CBTp) training in the U.S. and Canada. Psychosis. 2022;14:1–11.

    Article  Google Scholar 

  12. Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021;372: n71.

    Article  PubMed  PubMed Central  Google Scholar 

  13. WHO. The ICD-10 Classification of Mental and Behavioural Disorders: Diagnostic criteria for research. 1992. https://www.who.int/classifications/icd/en/GRNBOOK.pdf?ua=1.

  14. American Psychiatric Association. Diagnostic and statistical manual of mental disorders (5th ed). 2013. https://doi.org/10.1176/appi.books.9780890425596.

  15. The Joanna Briggs Institute. The Joanna Briggs Institute Critical Appraisal tools for use in JBI Systematic Reviews: Checklist for Prevalence Studies. 2017. https://jbi.global/research/critical-appraisal-tools.html.

  16. Munn Z, Moola S, Riitano D, Lisy K. The development of a critical appraisal tool for use in systematic reviews addressing questions of prevalence. Int J Health Policy Manag. 2014;3(3):123–8.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Nyaga VN, Arbyn M, Aerts M. Metaprop: a Stata command to perform meta-analysis of binomial data. Archives of Public Health. 2014;72(1):39.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Borenstein M, Hedges L, Rothstein H. Meta-analysis: Fixed effect vs. random effects. Meta-analysis com. 2007.

  19. Breitborde NJK, Bell EK, Dawley D, Woolverton C, Ceaser A, Waters AC, et al. The Early Psychosis Intervention Center (EPICENTER): development and six-month outcomes of an American first-episode psychosis clinical service. BMC Psychiatry. 2015;15(1):266.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Clarke AM, McLaughlin P, Staunton J, Kerins K, Power B, Kearney K, et al. Retrospective study of first episode psychosis in the Dublin Southwest Mental Health Service: demographics, clinical profile and service evaluation of treatment. Ir J Psychol Med. 2019;36(4):249–58.

    Article  PubMed  Google Scholar 

  21. Rathod S, Thorne K, Graves E, Phiri P, Asher C, Griffiths A, et al. Results of a prospective, mixed methods study to assess feasibility, acceptability and effectiveness of TRIumPH (Treatment and Recovery In PsycHosis): an integrated care pathway for psychosis, compared to usual treatment. BMJ Open. 2020;10: e033711.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Johns L, Jolley S, Garety P, Khondoker M, Fornells-Ambrojo M, Onwumere J, et al. Improving access to psychological therapies for people with severe mental illness (IAPT-SMI): lessons from the South London and Maudsley psychosis demonstration site. Behav Res Ther. 2019;116:104–10.

    Article  PubMed  Google Scholar 

  23. Haddock G, Eisner E, Boone C, Davies G, Coogan C, Barrowclough C. An investigation of the implementation of NICE-recommended CBT interventions for people with schizophrenia. J Ment Health. 2014;23(4):162–5.

    Article  PubMed  Google Scholar 

  24. Fischler I, Riahi S, Stuckey MI, Klassen PE. Implementation of a clinical practice guideline for schizophrenia in a specialist mental health center: an observational study. BMC Health Serv Res. 2016;16(1):372.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Royal College of Psychiatrists. National Clinical Audit of Psychosis - National Report for the Early Intervention in Psychosis Audit 2019/20202020. www.rcpsych.ac.uk/NCAP.

  26. Royal College of Psychiatrists. National Clinical Audit of Psychosis - Wales National Report for the Early Intervention of Psychosis Audit 2019/20202020. www.rcpsych.ac.uk/NCAP.

  27. Greenfield P, Joshi S, Christian S, Lekkos P, Gregorowicz A, Fisher HL, et al. First episode psychosis in the over 35 s: is there a role for early intervention? Early Interv Psychiatry. 2018;12(3):348–54.

    Article  PubMed  Google Scholar 

  28. Harvey C, Lewis J, Farhall J. Receipt and targeting of evidence-based psychosocial interventions for people living with psychoses: findings from the second Australian national survey of psychosis. Epidemiol Psychiatr Sci. 2019;28(6):613–29.

    Article  CAS  PubMed  Google Scholar 

  29. Colling C, Evans L, Broadbent M, Chandran D, Craig TJ, Kolliakou A, et al. Identification of the delivery of cognitive behavioural therapy for psychosis (CBTp) using a cross-sectional sample from electronic health records and open-text information in a large UK-based mental health case register. BMJ Open. 2017;7(7): e015297.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Coentre R, Mendes T, Rebelo A, Fonseca A, Levy P. PROFIP: A Portuguese early intervention programme for first-episode psychosis in Lisbon. Early Interv Psychiatry. 2019;13(6):1525–9.

    Article  PubMed  Google Scholar 

  31. Molag M, Beckers T, Mortel H. The implementation of the multidisciplinary guidelines for treatment of schizophrenia in teams for flexible assertive community treatment: a retrospective study of patient files. Tijdschr Psychiatr. 2018;60:521–6.

    CAS  PubMed  Google Scholar 

  32. Dubreucq J, Ycart B, Gabayet F, Perier CC, Hamon A, Llorca PM, et al. Towards an improved access to psychiatric rehabilitation: availability and effectiveness at 1-year follow-up of psychoeducation, cognitive remediation therapy, cognitive behaviour therapy and social skills training in the FondaMental Advanced Centers of Expertise-Schizophrenia (FACE-SZ) national cohort. Eur Arch Psychiatry Clin Neurosci. 2019;269(5):599–610.

    Article  PubMed  Google Scholar 

  33. Bioque M, Mezquida G, Amoretti S, García-Rizo C, López-Ilundain JM, Diaz-Caneja CM, et al. Clinical and treatment predictors of relapse during a three-year follow-up of a cohort of first episodes of schizophrenia. Schizophr Res. 2022;243:32–42.

    Article  PubMed  Google Scholar 

  34. Mason A, Irving J, Pritchard M, Sanyal J, Colling C, Chandran D, et al. Association between depressive symptoms and cognitive-behavioural therapy receipt within a psychosis sample: a cross-sectional study. BMJ Open. 2022;12(5): e051873.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Addington D, McKenzie E, Smith H, Chuang H, Boucher S, Adams B, et al. Conformance to evidence-based treatment recommendations in schizophrenia treatment services. Can J Psychiatry. 2012;57(5):317–23.

    Article  PubMed  Google Scholar 

  36. Coleman KJ, Stewart C, Waitzfelder BE, Zeber JE, Morales LS, Ahmed AT, et al. Racial-ethnic differences in psychiatric diagnoses and treatment across 11 health care systems in the mental health research network. Psychiatr Serv. 2016;67(7):749–57.

    Article  PubMed  PubMed Central  Google Scholar 

  37. Oluwoye O, Stokes B, Stiles B, Monroe-DeVita M, McDonell MG. Understanding differences in family engagement and provider outreach in New Journeys: a coordinated specialty care program for first episode psychosis. Psychiatry Res. 2020;291: 113286.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Lieberman JA, Stroup TS, McEvoy JP, Swartz MS, Rosenheck RA, Perkins DO, et al. Effectiveness of Antipsychotic Drugs in Patients with Chronic Schizophrenia. N Engl J Med. 2005;353(12):1209–23.

    Article  CAS  PubMed  Google Scholar 

  39. Roe D, Mashiach-Eizenberg M, Garber Epstein P, Yamin A, Hoter Ishay G, Zisman-Ilani Y. Implementation of NAVIGATE for first episode psychosis in Israel: Clients’ characteristics, program utilization and ratings of change. Early Interv Psychiatry. 2021;15(5):1343–8.

    Article  PubMed  Google Scholar 

  40. Switzer F, Harper SF. A narrative review of the barriers to the implementation of cognitive behavioural therapy for psychosis. Psychosis. 2019;11(2):151–61.

    Article  Google Scholar 

  41. Bucci S, Berry K, Barrowclough C, Haddock G. Family interventions in psychosis: a review of the evidence and barriers to implementation. Aust Psychol. 2016;51(1):62–8.

    Article  Google Scholar 

  42. Prytys M, Garety PA, Jolley S, Onwumere J, Craig T. Implementing the NICE guideline for schizophrenia recommendations for psychological therapies: a qualitative analysis of the attitudes of CMHT staff. Clin Psychol Psychother. 2011;18(1):48–59.

    Article  CAS  PubMed  Google Scholar 

  43. Lecomte T, Samson C, Naeem F, Schachte L, Farhall J. Implementing cognitive behavioral therapy for psychosis: An international survey of clinicians’ attitudes and obstacles. Psychiatr Rehabil J. 2018;41(2):141–8.

    Article  PubMed  Google Scholar 

  44. Ignatova D, Kamusheva M, Petrova G, Onchev G. Costs and outcomes for individuals with psychosis prior to hospital admission and following discharge in Bulgaria. Soc Psychiatry Psychiatr Epidemiol. 2019;54(11):1353–62.

    Article  PubMed  Google Scholar 

  45. Matić K, Gereš N, Gerlach J, Prskalo-Čule D, Zadravec Vrbanc T, Lovretić V, et al. Early intervention services for early-phase psychosis—centre for integrative psychiatry in Psychiatric Hospital “Sveti Ivan.” Croatia Psychiatria Danubina. 2018;30(Suppl 4):158–65.

    PubMed  Google Scholar 

  46. Patel V, Xiao S, Chen H, Hanna F, Jotheeswaran AT, Luo D, et al. The magnitude of and health system responses to the mental health treatment gap in adults in India and China. Lancet. 2016;388(10063):3074–84.

    Article  PubMed  Google Scholar 

  47. Aceituno D, Mena C, Vera N, Gonzalez-Valderrama A, Gadelha A, Diniz E, et al. Implementation of early psychosis services in Latin America: A scoping review. Early Interv Psychiatry. 2020;15:1104.

    Article  PubMed  Google Scholar 

  48. Mirza A, Birtel MD, Pyle M, Morrison AP. Cultural differences in psychosis: the role of causal beliefs and stigma in White British and South Asians. J Cross Cult Psychol. 2019;50(3):441–59.

    Article  Google Scholar 

  49. Bedard TE, Nadin S, Zufelt C, Cheng C. Implementation and evaluation of a quality improvement project: carepaths for Early Psychosis Intervention Programmes in Northeastern Ontario. Early Interv Psychiatry. 2016;10(6):547–53.

    Article  PubMed  Google Scholar 

  50. Cotter J, Zabel E, French P, Yung AR. Prolonged duration of untreated psychosis: a problem that needs addressing. Early Interv Psychiatry. 2017;11(3):263–8.

    Article  PubMed  Google Scholar 

  51. North CS, Simic Z, Burruss J. Design, implementation, and assessment of a public comprehensive specialty care program for early psychosis. J Psychiatr Pract. 2019;25(2):91–102.

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

Not applicable.

Author information

Authors and Affiliations

Authors

Contributions

SB, GT, and PJ led the design of the study. SB, EN, BV, NS & AN contributed to running searches, screening records, and extracting data. SB led the analysis of the data, supervised by GT and PJ. All authors contributed to data interpretation. SB wrote the initial draft of the manuscript, and all authors contributed to revising and finalising the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Pamela Jacobsen.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1.

Database search terms

Additional file 2: Figure S1.

Pooled prevalence of service-users who were offered CBTp. Figure S2. Pooled prevalence of service-users who received CBTp in countries with defined treatment guidelines. Figure S3. Pooled prevalence of service-users who received CBTp in countries where treatment guidelines were not available. Figure S4. Pooled prevalence of service-users who received CBTp_EI only. Figure S5. Pooled prevalence of service-users who received FI_EI only. Table S1. Summary of other recommended therapies. Table S2. Summary of predictors of therapy receipt.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Burgess-Barr, S., Nicholas, E., Venus, B. et al. International rates of receipt of psychological therapy for psychosis and schizophrenia: systematic review and meta-analysis. Int J Ment Health Syst 17, 8 (2023). https://doi.org/10.1186/s13033-023-00576-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13033-023-00576-9

Keywords