Introduction
Common mental disorders (CMDs) such as depression and anxiety cause considerable burden to both individuals and the economy, with an estimated 72 million working days lost each year (Centre for Mental Health, 2017). In England alone, one in six adults experience a CMD in a given week (Mcmanus, Bebbington, Jenkins, & Brugha, Reference Mcmanus, Bebbington, Jenkins and Brugha2016). Left untreated, CMDs can result in poor physical, social and occupational functioning and premature death (Stansfeld, Fuhrer, & Head, Reference Stansfeld, Fuhrer and Head2011; Zivin et al., Reference Zivin, Yosef, Miller, Valenstein, Duffy, Kales and Kim2015). In the UK, there are ethnic inequalities in seeking and receiving mental health treatment (Cooper et al., Reference Cooper, Spiers, Livingston, Jenkins, Meltzer, Brugha and Bebbington2013; Grey, Sewell, Shapiro, & Ashraf, Reference Grey, Sewell, Shapiro and Ashraf2013; Sizmur & McCulloch, Reference Sizmur and McCulloch2016). Racial and ethnic minority groups may have an increased vulnerability to CMDs through experiences of racism and discrimination (Hatch et al., Reference Hatch, Gazard, Williams, Frissa, Goodwin and Hotopf2016; Karlsen, Nazroo, McKenzie, Bhui, & Weich, Reference Karlsen, Nazroo, McKenzie, Bhui and Weich2005; Wallace, Nazroo, & Bécares, Reference Wallace, Nazroo and Bécares2016), and being more likely to experience social inequalities that can contribute to mental ill-health (Allen, Balfour, Bell, & Marmot, Reference Allen, Balfour, Bell and Marmot2014; Marmot & Bell, Reference Marmot and Bell2012). Delayed access to psychological support for CMDs can have a substantial negative impact on quality of life and functioning and can lead to CMDs developing into disorders more difficult to treat (Stansfeld et al., Reference Stansfeld, Fuhrer and Head2011).
In 2007, only a quarter of individuals diagnosed with CMDs were receiving appropriate specialist care in the UK (Layard, Clark, Knapp, & Mayraz, Reference Layard, Clark, Knapp and Mayraz2007). As a result, the Improving Access to Psychological Therapies (IAPT) programme was launched to provide equitable access to evidence-based psychological interventions for people experiencing CMDs (Clark, Reference Clark2011). Each clinical commissioning group across England is responsible for funding health services for their local area and providing their own IAPT services (NHS Digital, 2020). As such, there may be slight area level variations in the way these services are run, i.e. location of service delivery (GP surgeries, hospitals, community centres), the interventions available and level of service advertisement (British Association for Counselling and Psychotherapy, 2016; National Collaborating Centre for Mental Health, 2020) – all of which potentially impact on performance indicators such as waiting times and treatment outcomes. It is therefore important to also consider how the area in which service users live, i.e. their borough or locality of IAPT service, may impact treatment pathways.
Despite evidence of ethnic inequalities in wider mental health service use, there is a lack of research into referral and treatment pathways for racial and ethnic minority service user groups accessing IAPT. Of the limited existing research, studies examining ethnic differences in IAPT access and outcomes used data from the initial IAPT pilot sites between 2006 and 2010, which may now present an outdated representation of IAPT services. These initial studies found racial and ethnic minority groups were underrepresented in IAPT services, being less likely to be referred into the service than White groups (de Lusignan, Chan, Parry, Dent-Brown, & Kendrick, Reference de Lusignan, Chan, Parry, Dent-Brown and Kendrick2012; Parry et al., Reference Parry, Barkham, Brazier, Dent-, Hardy and Kendrick2011.), and greater proportions of Black and Asian service users accessed services via self-referral rather than their general practitioner (GP) (Clark et al., Reference Clark, Layard, Smithies, Richards, Suckling and Wright2009; Parry et al., Reference Parry, Barkham, Brazier, Dent-, Hardy and Kendrick2011.). An IAPT service in south London offering a self-referral option between 2009 and 2010 was shown to lead to more equitable access to psychological therapies for racial and ethnic minority groups compared to GP-referral (Brown et al., Reference Brown, Ferner, Wingrove, Aschan, Hatch and Hotopf2014). This reflects inequalities in wider mental health service use among racial and ethnic minority groups in the UK; survey findings also suggest that racial and ethnic minority groups are less likely to seek help for CMDs through primary care than their White counterparts (National Psychiatric Morbidity Survey – Cooper et al., Reference Cooper, Spiers, Livingston, Jenkins, Meltzer, Brugha and Bebbington2013), or to receive any treatment for mental ill-health (medication, counselling or both), with Black groups least likely to receive treatment (Adult Psychiatric Morbidity Survey Mcmanus et al., Reference Mcmanus, Bebbington, Jenkins and Brugha2016). All IAPT service users are now able to self-refer. Analysis of current IAPT data is required to determine whether and the extent to which such inequalities in service provision still persist.
Identifying inequalities in referral and treatment pathways of IAPT services for racial and ethnic minority service users is crucial for ensuring equity of access and the provision of appropriate, evidence-based NHS mental health care for these groups. The current study aimed to examine variation by ethnicity in (1) source of referral, (2) receipt of an initial assessment following referral, and (3) receipt of at least one treatment session within an IAPT service. The impact of the area (specific borough) of IAPT service on outcomes was examined for each aim. We hypothesised that compared to the White British service user group, IAPT service users from racial and ethnic minority groups would be (i) more likely to self-refer than be referred by a GP, (ii) less likely to receive an assessment and (iii) less likely to receive a treatment session.
Method
Setting and data source
The South London and Maudsley (SLaM) NHS Foundation Trust provides access to psychological therapies across four South London boroughs; Croydon, Lambeth, Lewisham and Southwark. Each borough implements their own IAPT services, with the majority of referrals coming from GPs or via self-referral. The service implements a stepped-care model to ensure that service users are offered the least-intrusive appropriate intervention first (National Collaborating Centre for Mental Health, 2020). Low intensity interventions may include self-help programmes, online cognitive behavioural therapy or group interventions. High intensity treatments are often a form of individual therapy but can include other intervention methods. Service users can be stepped up to high intensity or stepped down to low intensity as required (NHS Digital, 2018a).
IAPT services provide treatment for people with common mental health problems, including; depression, generalised anxiety disorder, social anxiety disorder, panic disorder, agoraphobia, OCD, phobias, PTSD, health anxiety and body dysmorphic disorder. For more information on referral criteria please see online Supplementary Material B.
Routine clinical data from the IAPTus electronic service user database (http://www.iaptus.co.uk) were exported to the Clinical Record Interactive Search (CRIS) system at SLaM, which provides pseudo-anonymised electronic health record data for the purposes of research analysis (Stewart et al., Reference Stewart, Soremekun, Perera, Broadbent, Callard, Denis and Lovestone2009).
Participants
Participants were adults (aged 16 years and older) who had been referred into IAPT services provided by SLaM between 1st January 2013 (when all four boroughs had established IAPT services) and 31st December 2016 (N = 85 800). Some individuals were referred more than once during the specified time period. To ensure independence of data, only the first treatment episode per person was included in the analysis.
Measure of referral source
Referral source was extracted from structured fields in IAPTus and were categorised into GP referral, self-referral, secondary health services or community service referral. Secondary health services included secondary mental health services, hospital services and outpatient clinics. Community services included statutory services such as Job Centre Plus (a government-funded employment agency), voluntary organisations, education providers and criminal justice (prison and probation services).
Measure of assessment and treatment
If there was at least one service user session record that had a purpose of ‘assessment’ and it was attended, the service user was categorised as having received an assessment (1 = assessed, 0 = not assessed). A service user was categorised as having received treatment if at least one of their session records had a purpose of ‘treatment’ (1 = treated, 0 = not treated). The latter analysis was restricted to those who had been assessed.
Measures of demographic characteristics
Service user gender (male, female) and exact age were recorded in IAPTus. Age was collapsed into age bands for descriptive purposes (16–24, 25–34, 35–44, 45–54, 55–64 and 65+ years), exact age was used for all age-adjusted models. Information on the ethnicity of the service user was collected at triage or initial assessment. The 17 ethnicity categories from the UK Census and used in IAPTus were recoded into White British, Black Caribbean, Black African, Black Other, Asian, Mixed, White Other and Other. The black ethnic group was disaggregated into three categories because sample size was sufficient enough to do so and we felt it important to explore black ethnicities separately due to their distinct experiences.
Measures of mental health
Patient health questionnaire depression scale
Symptoms of depression were measured using the validated nine-item Patient Health Questionnaire (PHQ-9; Kroenke, Spitzer, and Williams, Reference Kroenke, Spitzer and Williams2001). A PHQ-9 score ⩾10 is considered to be of clinical significance (sensitivity of 88% and a specificity of 88% for major depression) and is used as a cut-off to identify caseness in IAPT (National Collaborating Centre for Mental Health, 2020). Both the internal consistency and test−retest reliability of the PHQ-9 is excellent (Cronbach α = 0.89, intraclass correlation = 0.84).
Generalised anxiety disorder scale
Symptoms of anxiety were measured using the validated seven-item generalised anxiety disorder assessment (GAD-7; Spitzer, Kroenke, Williams, and Löwe, Reference Spitzer, Kroenke, Williams and Löwe2006). A score of ⩾8 has a sensitivity of 89% and a specificity of 82% and is used as a cut-off point for caseness in IAPT (National Collaborating Centre for Mental Health, 2020). The internal consistency of the GAD-7 is excellent (Cronbach α = 0.92). Test−retest reliability is also good (intraclass correlation = 0.83).
For the purposes of these analyses, scores collected at the initial contact stage, prior to assessment, were used to measure baseline symptoms of depression and anxiety.
Statistical analysis
Missing data
A total of 85 800 SLaM IAPT service users from 2013 to 2016 over the age of 16 were identified. There was missing data on some outcome and exposure variables – 0.7% of the sample (n = 593) had missing data on method of referral, 0.1% (n = 91) of the sample had missing data on gender and 18.5% (n = 15 917) had missing ethnicity data.
Though the amount of missing data for method of referral and gender is negligible, the amount of missing ethnicity data is substantial, particularly as ethnicity is the focal point of this study. Low levels of recording for ethnicity is an issue that typically constrains studies using health record data (Aspinall & Jacobson, Reference Aspinall and Jacobson2007; Kumarapeli, Stepaniuk, De Lusignan, Williams, & Rowlands, Reference Kumarapeli, Stepaniuk, De Lusignan, Williams and Rowlands2006; Mathur et al., Reference Mathur, Bhaskaran, Chaturvedi, Leon, vanStaa, Grundy and Smeeth2014). Often, missing ethnicity data are addressed by removing ethnicity from the analysis entirely (complete case analysis) (Osborn et al., Reference Osborn, Hardoon, Omar, Holt, King, Larsen and Petersen2015), or by performing single imputation of missing values with the White ethnic group (Hippisley-Cox et al., Reference Hippisley-Cox, Coupland, Vinogradova, Robson, Minhas, Sheikh and Brindle2008) − these methods generally lead to biased estimates of association and standard errors (Sterne et al., Reference Sterne, White, Carlin, Spratt, Royston, Kenward and Carpenter2009). Multiple imputation (MI) is another common method of addressing missing data. However, the probability that ethnicity is recorded in primary care may well vary systematically by ethnic group, even after adjusting for other variables (Mathur et al., Reference Mathur, Bhaskaran, Chaturvedi, Leon, vanStaa, Grundy and Smeeth2014).This implies a potential missing not at random (MNAR) mechanism for ethnicity, and as a result, standard MI might fail to give valid reference for the underlying population.
Weighted MI can be used to address the specific problem of MNAR ethnicity data in health records and overcome the limitations of the more commonly used methods mentioned (Pham, Morris, & Petersen, Reference Pham, Morris and Petersen2015). Weighted MI combines MI and probability weights which are calculated using marginal population distribution of ethnicity available in the UK census data. Census summary statistics for ethnicity provide weights which inform the MI such that the imputed dataset better reflects the ethnicity of the population in question (in this instance, residents of the four boroughs which comprise SLaM) and not that of the complete data. Several studies have found this to reduce bias compared to standard MI methods (Pham et al., Reference Pham, Morris and Petersen2015; Pham, Carpenter, Morris, Wood, & Petersen, Reference Pham, Carpenter, Morris, Wood and Petersen2019). This method assumes that a particular service user group is somewhat representative of the population, which may not always be the case. Racial and ethnic minority populations experience barriers to care and are less likely to engage with health services (Cooper et al., Reference Cooper, Spiers, Livingston, Jenkins, Meltzer, Brugha and Bebbington2013; Mcmanus et al., Reference Mcmanus, Bebbington, Jenkins and Brugha2016). However, self-referral options (such as those provided by IAPT) have been shown to lead to more equitable provision of psychological therapies for racial and ethnic minority groups compared to GP-referral (Brown et al., Reference Brown, Ferner, Wingrove, Aschan, Hatch and Hotopf2014; Parry et al., Reference Parry, Barkham, Brazier, Dent-, Hardy and Kendrick2011.). Therefore, although this weighted MI approach may overestimate proportions of racial and ethnic minority service users (because these populations can be underrepresented in healthcare), IAPT's self-referral options may mitigate against this underrepresentation.
To ensure a robust analysis, this study reports the findings of analyses from (i) complete case data and (ii) an imputed dataset where ethnicity has been imputed using weighted MI, utilising 2011 census data on ethnicity for Croydon, Lambeth, Lewisham and Southwark (see online Supplementary Material C for these Census data). In addition, analysis of data where ethnicity has been imputed using a more standard approach – multiple imputation with chained equations (MICE) (White, Royston, & Wood, Reference White, Royston and Wood2011) – will be reported in online Supplementary Material D. Findings from the MICE imputed dataset will be commented on in manuscript if they contradict findings from either complete case or weighted mi datasets.
The proportion of missing ethnicity data varied across boroughs; 6% of data from Lewisham was missing, 8% from Lambeth, 30% from Croydon and 34% from Southwark. As such, the socio-demographic characteristics and prevalence of anxiety and depression among service users, as well as the main outcomes of this study, will be broken down by borough.
Analysis
Data analyses were conducted using Stata 15 (StataCorp, 2019). Descriptive statistics were calculated to describe the analytic sample by ethnicity, age, gender, borough of service, depression and anxiety symptoms, referral source, receipt of an assessment and of at least one treatment session (among those assessed). Due to each borough implementing its own IAPT service and the potential differences this may pose for service user pathways to treatment, borough was adjusted for separately to explore the impact of borough of service on the outcomes of interest. Therefore, to examine variation by ethnicity in IAPT referral source, multinomial regression analyses were conducted; unadjusted (model 1), adjusting for age and gender and year of referral (model 2), and adjusting to additionally include borough of service (model 3). Relative risk ratios (RRRs) with 95% confidence intervals (CI) are reported. Next, logistic regression analysis was used to determine whether ethnicity was associated with (i) receiving an assessment session, and (ii) receipt of at least one IAPT treatment session (among those who were assessed). Odds ratios (ORs) with 95% CI are reported. These analyses were also adjusted for age, gender, year of referral and borough in the same manner. Interaction effects were also tested using a Wald test to compare models with and without an interaction term to determine whether borough moderated the effect of ethnicity on any of the main outcomes.
In our examination of variations in referral source, assessment, and treatment by ethnicity, we will first report findings where there were no discrepancies between imputed and complete case data and then highlight discrepant findings.
Results
The characteristics of the sample are shown in Table 1. The majority of the sample identified as White British (52.4%), female (63.0%) and were referred to IAPT services in Lambeth (30.9%). The largest racial and ethnic minority groups were Black Caribbean (12.0%) and White Other (12.4%), and over a third of the sample were aged between 25 and 34 years (33.5%). Upon referral, 77.6% of the sample met caseness for depression and 82.2% for anxiety. Most referrals to IAPT services were via primary care (54.3%) or self-referral (40.3%). The majority of the sample had received an assessment session (64.9%) and of those, over two-thirds received at least one treatment session thereafter (70.4%). See online Supplementary Material A for a breakdown of sample characteristics by ethnicity.
Table 1. Characteristics of service users aged 16 + referred to IAPT services between 2013 and 2016 across the four London borough that comprise SLaM
Community services include: voluntary sector organisations, government service providers, education providers and criminal justice referrals (prison and probation services).
a Missing referral method data on n = 462.
Variations in referral source
Self-referral
Analysis of weighted MI data found that, following all stages of adjustment, compared to the White British group, Black African (OR 0.67, CI 0.63–0.71), Asian (OR 0.65, CI 0.61–0.69) and Mixed ethnic groups (OR 0.80, CI 0.76–0.84) were less likely to self-refer than be referred through their GP (see Table 2). This was also found in the complete case data.
Table 2. Association between ethnic groups and method of referral to IAPT services treatment [referral by general practitioner (GP) is the reference]
Weighted MI is the process of replacing missing data with substituted values as informed by complete data and marginal population level data. It is used here to address missing ethnicity data.
Numbers (n), percentages (%),RRRs and 95% CI are shown.
Though not detected in the complete case or MICE imputed datasets, the weighted MI data also indicated that the Black Other (OR 0.68, CI 0.62–0.76), White Other (OR 0.81, CI 0.75–0.87) and Other (OR 0.83, CI 0.74–0.94) ethnic groups were also less likely to self-refer than be referred through their GP compared to the White British ethnic group.
Secondary care
Analysis of weighted MI data found that, compared to the White British group, Asian (OR 1.24, CI 1.08–1.41) and Black Caribbean (OR 1.16, CI 1.01–1.33) groups were more likely to be referred to IAPT via secondary care than their GP following all levels of adjustment. This was found in both complete case and weighted MI datasets.
Community services
Analysis of the weighted MI dataset found that, compared to the White British service users, Black Caribbean (OR 1.92, CI 1.65–2.24), Black Other (OR 2.62, CI 2.03–3.38) and White Other (OR 1.85, CI 1.52–2.24) groups were more likely to be referred through community services than via their GP following all levels of adjustment. Black African (OR 1.77, CI 1.43–2.19) and Asian groups (OR 1.64, CI 1.38–1.94) were also more likely to be referred through community services in fully adjusted models. This was also found in the complete case data.
Though not detected in the weighted MI data, both complete case data and MICE imputed data found that the Mixed ethnic group was less likely to be referred through community services (OR 0.77, CI 0.63–0.95).
Due to low cell count, interaction effects to identify whether borough moderates the association between ethnicity and referral source could not be tested for.
Variations in assessment receipt
Compared to the White British ethnic group, analysis of both the complete case and the weighted MI datasets indicated that the Black Caribbean, Black African, Black Other, Asian, Mixed and White Other ethnic groups were less likely to receive an assessment following referral (see Table 3). These associations remained significant following all levels of adjustment.
Table 3. Associations between ethnic groups and receiving an assessment after being referred to IAPT with the use of logistic regression analysis
Weighted MI is the process of replacing missing data with substituted values as informed by complete data and marginal population level data. It is used here to address missing ethnicity data.
Numbers (n), percentages (%),OR and 95% CI are shown.
Analysis of the weighted MI dataset also indicated that the Other ethnic group was significantly less likely to receive an assessment following all levels of adjustment (OR 0.55, CI 0.49–0.61). This is in contrast to the analysis of the complete case dataset which found a positive non-significant association (OR 1.10, CI 0.97–1.25) – these findings from the complete case analysis are supported by the findings from the MICE imputed dataset (see online Supplementary Material D).
Borough of service was found to significantly moderate the effect of ethnicity on receiving an assessment (p < 0.01, χ2 = 71, df = 21).
Variations in treatment receipt
Findings from both the complete case and weighted MI datasets indicate that, among service users who received an assessment, compared to the White British group all other ethnic groups (with the exception of the Mixed ethnic group) were less likely to receive treatment (see Table 4). The Mixed ethnic group was only significantly less likely to receive treatment after adjusting for age, gender, year of referral and borough. For other levels of adjustment this association was non-significant for the Mixed ethnic group in both complete case and weighted MI datasets (OR 0.93, CI 0.88–1.00).
Table 4. Associations between ethnic group and treatment receipt among those assessed with the use of logistic regression analysis
Weighted MI is the process of replacing missing data with substituted values as informed by complete data and marginal population level data. It is used here to address missing ethnicity data.
Numbers (n), percentages (%),OR and 95% CI are shown.
Borough was not found to significantly moderate the effect of ethnicity on receiving treatment (p > 0.05, χ2 = 32, df = 21).
Reason for not receiving assessment for treatment
Service users may not receive an assessment or treatment for a variety of reasons; either they did not attend assessment/treatment or dropped out, were discharged, declined treatment, treatment was not suitable for them, or they were referred elsewhere. Percentages across all ethnic groups are not dissimilar (as shown in Table 5). However, in terms of those in the sample who did not receive an assessment, Black African service users had the highest percentage for declining as assessment out of all ethnic groups (26.5%), and Black Other service users had the highest percentage for being referred elsewhere out of all ethnic groups (19%). In terms of those who did not receive treatment following an assessment, no major disparities were shown between ethnic groups.
Table 5. Available data on reason for end-of-care pathway
a e.g. specialist service or community mental health team.
b n = 18 541 due to missing ethnicity data.
c n = 15 110 due to missing ethnicity data.
Discussion
This study utilised electronic IAPT records to identify ethnic inequalities in the method of referral to IAPT services and whether the odds of receiving an assessment and/or initiating treatment varied by ethnicity. The analysis in this study was restricted to the four south London boroughs that fall within the remit of an NHS foundation trust that specialises in and is the sole provider for mental health services in these areas. These boroughs are ethnically diverse and have a greater number of Black Caribbean residents than other London boroughs. This study was able to further examine where disparities in access to and uptake of mental health care for CMDs are experienced by racial and ethnic minority service users, and importantly, highlighted differences between these groups through disaggregating ethnicity. Overall, our findings indicate that racial and ethnic minority groups were less likely to self-refer to IAPT than the White British group and were more likely to be referred via community services. Most racial and ethnic minority groups were also less likely to receive an assessment after being referred and those assessed were also less likely to receive a treatment session than the White British group.
Method of referral
In contrast to literature demonstrating that self-referral may improve access to IAPT for racial and ethnic minority groups (Brown et al., Reference Brown, Ferner, Wingrove, Aschan, Hatch and Hotopf2014; Parry et al., Reference Parry, Barkham, Brazier, Dent-, Hardy and Kendrick2011), we found many racial and ethnic minority groups to be less likely to self-refer than the White British group; contradicting our first hypothesis.
Disparities in referral pathways may be attributable to a mix of structural and cultural barriers. Self-referral to IAPT is commonly advised and sometimes expected by primary care clinicians as it allows their service users to ‘take ownership’ of their recovery (Thomas et al., Reference Thomas, Hansford, Ford, Wyatt, McCabe and Byng2020). However, qualitative interviews with low-income primary care service users highlighted that being advised to self-refer this could make them feel dismissed or invalidated by their GP after building the courage to seek help for their mental health (Thomas et al., Reference Thomas, Hansford, Ford, Wyatt, McCabe and Byng2020). Further, completing a self-referral via telephone call or online form could seem a challenging task to those dealing with difficulties such as low mood and anxiety. These experiences could exacerbate feelings of disconnect between GP and service user and may lead to individuals not self-referring as advised. Such experiences may also have increased detrimental impact for racial and ethnic minority service users. Literature shows these groups are already less likely to seek help for CMDs from primary care than White ethnic groups (Cooper et al., Reference Cooper, Spiers, Livingston, Jenkins, Meltzer, Brugha and Bebbington2013), may mistrust mental health services and professionals as a result of discrimination from the healthcare system, or may have previously experienced culturally insensitive or naïve interactions with health professionals (Bhui, Warfa, Edonya, McKenzie, & Bhugra, Reference Bhui, Warfa, Edonya, McKenzie and Bhugra2007; Henderson et al., Reference Henderson, Williams, Gabbidon, Farrelly, Schauman, Hatch and Clement2015; Memon et al., Reference Memon, Taylor, Mohebati, Sundin, Cooper, Scanlon and De Visser2016).
Additionally, cultural beliefs about mental health among some racial and ethnic groups can act as a barrier to care. For example, Black African women with experiences of depression were found to have thought the disorder was less serious and less amenable to psychological treatment than White British women (Brown, Boardman, Whittinger, & Ashworth, Reference Brown, Boardman, Whittinger and Ashworth2010). Some racial and ethnic minority groups, for example South Asian, may be less likely to perceive mental health problems as medical disorders that can be treated professionally, instead sometimes being attributable to the will of God or poor parenting (Rethink, 2010). We found racial and ethnic minority service users were more likely to have been referred to IAPT via community services, such as a government funded employment agency, voluntary organisations, education providers or criminal justice, than White British service users; this was especially pertinent for Black Caribbean and Black Other ethnic groups. This may be reflective of structural racism generating greater feelings of mistrust towards mental health services, with previous literature showing Black and African Caribbean groups to be over-represented in mental health services, experience worse outcomes and to be over four-times more likely to be detained under the Mental Health Act than White individuals (Bhui et al., Reference Bhui, Stansfeld, Hull, Priebe, Mole and Feder2003; McKenzie, Reference McKenzie2007; NHS Digital, 2018b; Sharpley, Hutchinson, McKenzie, & Murray, Reference Sharpley, Hutchinson, McKenzie and Murray2001). However, it may also reflect efforts by IAPT services to liaise with community services to address the under-referral of racial or ethnic minority individuals and highlights the successful work of community services at supporting access to treatment as well as the important role they can play in ensure the health needs of all populations are met.
Assessment and treatment
In fully adjusted models in both weighted MI and complete case datasets, almost all racial and ethnic minority groups had decreased odds of both receiving an assessment and of receiving at least one treatment session following assessment compared with those in the White British group. This supports our second and third hypotheses that racial and ethnic minority groups would be less likely than the White British group to receive both an assessment and a treatment session, and also supports previous literature that has found racial and ethnic minority groups to be less likely to receive any type of psychological treatment, medication or counselling (Cooper et al., Reference Cooper, Spiers, Livingston, Jenkins, Meltzer, Brugha and Bebbington2013; Mcmanus et al., Reference Mcmanus, Bebbington, Jenkins and Brugha2016; Sizmur & McCulloch, Reference Sizmur and McCulloch2016), or to be referred to specialist mental health services (Bhui et al., Reference Bhui, Stansfeld, Hull, Priebe, Mole and Feder2003). Similar proportions of service users across all racial and ethnic minority groups did not attend or dropped out of offered treatment, declined treatment or were referred elsewhere, giving no indication of disparities by ethnicity in reasons for not receiving treatment. Previous literature suggests that stigma around mental illness in certain cultures may result in treatment avoidance due to shame, fear or secrecy (Alvidrez, Snowden, & Kaiser, Reference Alvidrez, Snowden and Kaiser2008; Rethink, 2010; Shefer et al., Reference Shefer, Rose, Nellums, Thornicroft, Henderson and Evans-Lacko2013). However, it is important to note that discriminatory processes, structures and attitudes exist within mental health care that impact care quality and appropriateness for racial and ethnic minority service users (Joint Commissioning Panel for Mental Health, 2014). Limited research exists evidencing a positive relationship between cultural competency training and improved experiences for racial and ethnic minority health service users (Bennett & Keating, Reference Bennett and Keating2009; Healey et al., Reference Healey, Stager, Woodmass, Dettlaff, Vergara, Janke and Wells2017; Lie, Lee-Rey, Gomez, Bereknyei, & Braddock, Reference Lie, Lee-Rey, Gomez, Bereknyei and Braddock2011). Further, training in cultural competency may allude that inequality is due to the individual's cultural difference and not structural racial bias. IAPT must work towards addressing structural barriers to care, emphasise active anti-racist professional practice and allow for the exploration of racial inequality within their service (Bennett & Keating, Reference Bennett and Keating2009; Cénat, Reference Cénat2020). Addressing barriers to treatment are important; treatment avoidance or delay can lead to worsened CMD symptoms so that the level of severity becomes too high for the scope of IAPT practice.
The moderating effect of borough on the association between ethnicity and assessment suggests potentially unequal provision of care for different ethnic groups across the four boroughs that comprise SLaM. This would imply that both the service user's racial or ethnic background and their area of residence impacts the odds of entering the service. This interaction between ethnicity and borough must be addressed through substantial structural changes implemented across SLaM. Addressing the high proportion of missing ethnicity data from IAPT services in Croydon (30%) and Southwark (34%) – considerably higher than Lewisham (6%) and Lambeth (8%) – would be the first step in addressing the problem of unequal provision.
Strengths and limitations
Using a large dataset, this study demonstrated variation in the way that IAPT service users enter services by ethnicity, and that racial and ethnic minority service users are less likely to receive psychological treatment in IAPT services in four south London boroughs. However, explanations for our results remain speculative and it is unknown whether these individuals received psychological treatment elsewhere or not at all. Unfortunately, socio-economic data (to contextualise our analysis) and mental health prior to treatment (to establish need) were either unavailable to us through IAPT or the large amount of missing data. There is no information available to us in IAPTus about existing mental health diagnoses for those who are referred, we also have no information on those with a mental health need who were not referred to IAPT. Therefore, it is unknown whether these factors may have influenced individual's ability to engage with IAPT services.
We used electronic health record data to identify our dataset, which meant our study was dependent upon IAPT clinicians' input of accurate data. Missing data were an issue with this study, with 18.5% of service users not having data recorded for their ethnicity. This is unfortunately a common issue when utilising healthcare records, despite ethnicity being an incredibly important factor when examining healthcare provision and inequalities. To address this issue, ethnicity data were imputed using two different techniques and reported alongside the complete dataset. Overall results from both these datasets for all research questions were highly similar, increasing the validity of our conclusions.
Implications
Our findings pose implications for primary care clinicians in facilitating more racial and ethnic minority IAPT referrals, and for IAPT services to consider barriers specific to their racial and ethnic minority service users when engaging with the service. Racial and ethnic minority service users are more likely to be engaging with IAPT services after being referred through more adverse pathways, potentially indicating that their mental health may have been untreated for some time. Further research is needed to examine variation in the number of IAPT referrals by ethnicity and to understand why racial and ethnic minority service users are declining or dropping out of assessments and treatments in IAPT. Clinicians also need to be made aware of this issue and procedures introduced to improve engagement and retention.
Many racial and ethnic minority service users are less likely to self-refer than White British service users, which may mean that they are either unaware of this method of referral, experience more barriers to the use of this method, do not recognise their problems as being appropriate for psychological treatment, or do not trust IAPT services specifically or health services more generally. More effort should be made to gain the trust of racial and ethnic minority service users.
The missing data for ethnicity highlighted in this study is concerning, and more should be done by IAPT to ensure this information is recorded. Analysis of our weighted MI data sometimes highlighted starker ethnic inequalities than that found in the complete case and MICE datasets. This indicates that if the ethnic breakdown of SLaM IAPT service users does reflect that of the population across the boroughs, then due to the amount of missing ethnicity data in IAPT records, the extent of the ethnic inequalities in these boroughs is being obscured.
In addition, the intersections of ethnicity and migration status could not be considered in this study due to country of origin not being recorded in IAPTus. The distinct, and intersecting experiences of migrant service users also from a racial or ethnic minority group may differ greatly from those of British-born, racial and ethnic minority service users, considering migrants face specific barriers to engaging with health services (Gazard, Frissa, Nellums, Hotopf, & Hatch, Reference Gazard, Frissa, Nellums, Hotopf and Hatch2015), potential language limitations (Fountain & Hicks, Reference Fountain and Hicks2010; Memon et al., Reference Memon, Taylor, Mohebati, Sundin, Cooper, Scanlon and De Visser2016) and additional burdens of discrimination or underemployment following migration increasing vulnerability to CMDs (Das-Munshi, Leavey, Stansfeld, & Prince, Reference Das-Munshi, Leavey, Stansfeld and Prince2012; Hatch et al., Reference Hatch, Gazard, Williams, Frissa, Goodwin and Hotopf2016). Changes should be made to IAPTus to capture this information so that IAPT can cater for any specific needs of its migrant service users.
More could be done to ensure mental health services and psychometric measures are adapted to a culturally diverse population. For example, migrant groups may be more likely to require assistance with English language. Potential bias can arise when psychometric scales created from western understandings of mental health are directly translated into other languages (Searight & Searight, Reference Searight and Searight2009). Moreover, whilst SLaM IAPT services do offer interpreters to those who require them, being unable to communicate directly with their therapist can lead to issues detrimental to the therapeutic relationship. This might include problems expressing empathy to the client and impairments in the development of a shared understanding, which may deter from service engagement and lead to a poorer client satisfaction (Bowl, Reference Bowl2007; Fountain & Hicks, Reference Fountain and Hicks2010; Memon et al., Reference Memon, Taylor, Mohebati, Sundin, Cooper, Scanlon and De Visser2016; Tutani, Eldred, & Sykes, Reference Tutani, Eldred and Sykes2018). Interpreter availability can also cause delays in assessment and treatment appointments which could have negative effects on access or treatment benefit. As IAPT is a talking therapies service, these factors may influence migrant individuals' ability and desire to attend an assessment or treatment session. For consideration of these and other issues, IAPT have produced a positive practice guide for working with Black, Asian and minority ethnic service users (Beck, Naz, Brooks & Jankowska, Reference Beck, Naz, Brooks and Jankowska2019).
Conclusion
This study identifies inequalities in referral source, receipt of an assessment and receipt of treatment for racial and ethnic minority service users. These disparities may be due to a range of cultural, structural and practical barriers along the pathway. Future research making use of qualitative methods would enable exploration of IAPT pathways among racial and ethnic minority service users in more detail, allowing for the identification and exploration of factors and potential mechanisms that are contributing to the generation and perpetuation of these inequalities.
Supplementary material
The supplementary material for this article can be found at https://doi.org/10.1017/S0033291721002518
Acknowledgements
We would like to thank the National Institute for Health Research (NIHR) Biomedical Research Centre at South London and Maudsley NHS Foundation Trust.
Author contribution
SH conceived the TIDES study concept and design with input from BG. Data were prepared by SM and BG. HH and RR conducted the statistical analysis and wrote the article supervised by SH and CW. IB and ZC provided guidance on the analysis. JH and KA aiding with the interpretation of the data. All authors provided critical feedback on the manuscript.
Financial support
This work was supported by the Wellcome Trust [ 203380/Z/16/Z] and the National Institute for Health Research (NIHR) Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King's College London. CW is supported by and SLH are part supported by the Economic and Social Research Council (ESRC) Centre for Society and Mental Health at King's College London (ESRC Reference: ES/S 012567/1). IB and SLH are part-funded by the NIHR Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King's College London. IB is also supported by the NIHR Applied Research Collaboration South London (NIHR ARC South London) at King's College Hospital NHS Foundation Trust. The views expressed are those of the authors and not necessarily those of the funders, NHS, NIHR, Department of Health. The funders did not have a role in the study design; collection, analysis, or interpretation of data; the writing of the manuscript; or in the decision to submit the manuscript for publication.
Conflict of interest
None.
Ethical statement
This study received ethical approval from King's College London Research Ethics Committee for Psychiatry, Nursing and Midwifery (REC reference: HR-17/18-4629 – IRAS project ID: 230692). It also received approval from South London and Maudsley NHS Foundation Trust and was approved by the CRIS Oversight Committee.
Open access
