Introduction
It has been well documented that people with mental health problems report high levels of discrimination (Sibitz et al. Reference Sibitz, Amering, Unger, Seyringer, Bachmann, Schrank, Benesch, Schulze and Woppmann2011; Evans-Lacko et al. Reference Evans-Lacko, Brohan, Mojtabai and Thornicroft2012; Farrelly et al. Reference Farrelly, Clement, Gabbidon, Jeffery, Dockery, Lassman, Brohan, Henderson, Williams, Howard and Thornicroft2014; Griffiths et al. Reference Griffiths, Carron-Arthur, Parsons and Reid2014). There is an increasing effort to try to end discrimination towards people affected by mental health problems (Heinz et al. Reference Heinz, Charlet and Rapp2015; Mehta et al. Reference Mehta, Clement, Marcus, Stona, Bezborodovs, Evans-Lacko, Palacios, Docherty, Barley, Rose, Koschorke, Shidhaye, Henderson and Thornicroft2015; Thornicroft et al. Reference Thornicroft, Mehta, Clement, Evans-Lacko, Doherty, Rose, Koschorke, Shidhaye, O'Reilly and Henderson2015; Wahlbeck, Reference Wahlbeck2015; Weissman, Reference Weissman2015), with the promotion of anti-stigma programmes worldwide such as ‘Like Minds, Like Mine’ (Vaughan & Hansen, Reference Vaughan and Hansen2004; Thornicroft et al. Reference Thornicroft, Wyllie, Thornicroft and Mehta2014), ‘Opening Minds’ (Sartorius, Reference Sartorius2014; Stuart et al. Reference Stuart, Chen, Christie, Dobson, Kirsh, Knaak, Koller, Krupa, Lauria-Horner, Luong, Modgill, Patten, Pietrus, Szeto and Whitley2014), and ‘Open the Doors’ (Rüsch et al. Reference Rüsch, Angermeyer and Corrigan2005; Gaebel et al. Reference Gaebel, Zäske, Baumann, Klosterkötter, Maier, Decker and Möller2008; NHS Scotland, 2008; Thornicroft et al. Reference Thornicroft, Brohan, Kassam and Lewis-Holmes2008; Evans-Lacko et al. Reference Evans-Lacko, Brohan, Mojtabai and Thornicroft2012; Evans-Lacko et al. Reference Evans-Lacko, Corker, Williams, Henderson and Thornicroft2014a , Reference Evans-Lacko, Courtin, Fiorillo, Knapp, Luciano, Park, Brunn, Byford, Chevreul, Forsman, Gulacsi, Haro, Kennelly, Knappe, Lai, Lasalvia, Miret, O'Sullivan, Obradors-Tarragó, Rüsch, Sartorius, Svab, van Weeghel, Van Audenhove, Wahlbeck, Zlati, McDaid and Thornicroft b ).
The Time to Change (TTC) anti-stigma programme, England's largest programme aimed at reducing stigma and discrimination against people with mental health problems, started in 2007 (http://www.time-to-change.org.uk/) (Henderson et al. Reference Henderson, Evans-Lacko and Thornicroft2013). One of the main strategies of the TTC programme was to encourage service user leadership including events with the active involvement of mental health service users (i.e. ‘Get moving’, ‘Living libraries’ and ‘Education not discrimination’ activities) (Evans-Lacko et al. Reference Evans-Lacko, Malcolm, West, Rose, London, Rüsch, Little, Henderson and Thornicroft2013; Friedrich et al. Reference Friedrich, Evans-Lacko, London, Rhydderch, Henderson and Thornicroft2013). As part of the evaluation of TTC, and specifically to assess the effect of the programme on people with mental health problems, the Viewpoint survey was run annually to assess individuals' experience of discrimination within the previous 12 months (Henderson & Thornicroft, Reference Henderson and Thornicroft2009; Henderson et al. Reference Henderson, Corker, Lewis-Holmes, Hamilton, Flach, Rose, Williams, Pinfold and Thornicroft2012; Corker et al. Reference Corker, Hamilton, Henderson, Weeks, Pinfold, Rose, Williams, Flach, Gill, Lewis-Holmes and Thornicroft2013; Evans-Lacko, Reference Evans-Lacko, Corker, Williams, Henderson and Thornicroft2014a ). Moreover, in the field of overcoming discrimination, it is important to assess service users' responses to discriminatory experiences, which constitute the process of coping (Mendoza-Denton et al. Reference Mendoza-Denton, Page-Gould, Pietrzak, Levin and van Laar2006; Hinshaw, Reference Hinshaw2007). Coping strategies may represent a way for service users to reduce the level of discrimination they experience (Farrelly et al. Reference Farrelly, Jeffery, Rüsch, Williams, Thornicroft and Clement2015).
According to Stuart et al. (Reference Stuart, Arboleda-Florez and Sartorius2012), the most important contribution to the conceptualization and measurement of stigma coping is the work by Link et al. (Reference Link, Struening, Neese-Todd, Asmussen and Phelan2001). Link distinguished several coping orientations: ‘secrecy’, described as concealing labelling information; ‘education’, consisting in providing information to counter stereotypes; ‘withdrawal’, defined as avoiding potential rejecting situations; ‘distancing’, cognitive separation of the potentially stigmatised person from the stigmatised group; and ‘challenging’, active confrontation of stigmatising behaviour (Link et al. Reference Link, Phelan, Hatzenbuehler, McLeod, Lawler and Schwalbe2014). The TTC programme aims to enhance the ‘challenging’ and ‘educating’ strategies in people with mental health problems. Since 2011, to provide a baseline for the second phase of the TTC programme – which began in October 2011 – questions on coping with stigma based on Link et al. conceptualization (Reference Link, Mirotznik and Cullen1991, Reference Link, Struening, Neese-todd, Asmussen and Phelan2002) were added.
Coping strategies are far from being uniform among mental health service users. Research has found their endorsement is influenced by socio-demographic characteristics, variables related to mental health problems, and by the person's social functioning (Major & Townsend, Reference Major, Townsend, Dovidio, Hewstone, Glick and Esses2010; Moses, Reference Moses2015).
To the best of our knowledge, no previous studies have evaluated whether anti-stigma programmes are possible predictors of coping strategies adopted by people with mental health problems.
Our primary hypothesis was that having actively participated in programme activities would be more strongly associated with the use of both ‘challenging’ and ‘educating’ coping strategies, than just having seeing some of the social marketing campaign, as the programme seeks to both educate and challenge.
Methods
From 2008 to 2014, telephone interview surveys (the Viewpoint survey) were conducted annually. Each year, five National Health Service (NHS) mental health trusts across England were selected to take part. Different trusts and/or different regions within the same trusts were selected each year. Participants were recruited through NHS mental health trusts (service provider organisations). The target sample was 1000 individual interviews in each year. The inclusion criteria were: age between 18 and 65 years; having a diagnosis of any mental disorder; being in contact with the specialist mental health services in the previous 6 months. Patients who were not currently living in the community (e.g., were in prison or hospital) were excluded as well as patients with a diagnosis of dementia. A specific part of the Viewpoint survey was the use of interviewers with lived experience of mental health problems (Hamilton et al. Reference Hamilton, Pinfold, Rose, Henderson, Lewis-Holmes, Flach and Thornicroft2011).Telephone interviewers were trained and supervised by members of the research team. Allocation of participants to interviewers was based on interviewer availability. The detailed methodology is reported elsewhere (Hamilton et al. Reference Hamilton, Pinfold, Rose, Henderson, Lewis-Holmes, Flach and Thornicroft2011; Corker et al. Reference Corker, Hamilton, Henderson, Weeks, Pinfold, Rose, Williams, Flach, Gill, Lewis-Holmes and Thornicroft2013; Henderson et al. Reference Henderson, Corker, Hamilton, Williams, Pinfold, Rose, Webber, Evans-Lacko and Thornicroft2014).
Assessment tools
The primary outcome of the study was to assess the possible predictive role of participation in the TTC programme on mental health users' reported coping strategies as per Link et al. (Reference Link, Struening, Neese-todd, Asmussen and Phelan2002). Coping strategies were assessed through a modified version of the scale developed by Link et al. (Reference Link, Struening, Neese-todd, Asmussen and Phelan2002). According to the main characteristics of the TTC programme, based on the active involvement and participation of people with mental health problems, the ‘challenging’ and ‘educating’ coping strategies were evaluated (Henderson et al. Reference Henderson, Evans-Lacko and Thornicroft2013). The ‘challenging’ strategy is defined as people's orientation to confronting prejudice and discrimination. It assesses how likely respondents are to challenge stigmatising behaviour when it occurs or to disagree with people who make stigmatising statements. Items are scored on a 5-level Likert scale, ranging from 1 = never to 5 = often. The global score of the scale is the mean of five items, with higher score indicating higher endorsement of the strategy. The ‘educating’ strategy is described as the respondents' orientation to educating others in order to reduce the possibility of rejection. This subscale comprises three items, each item ranges on a 4-level Likert score, from 1 = strongly agree to 4 = strongly disagree. The global score of the scale is the mean of three items, with higher scores indicating higher level of experience of using this strategy. As suggested by Link et al. (Reference Link, Struening, Neese-todd, Asmussen and Phelan2002), the 2.5 midpoint of each subscale was considered as cut-off for evaluating whether the coping strategy was used or not.
Regarding the evaluation of the experience of the TTC programme, participants were asked a question, which had three possible answers: have seen some publicity; have participated in some activities; or have not seen any publicity of TTC programme. This variable was managed as a categorical variable, considering ‘have not seen any publicity of TTC programme’ as the reference category.
The Discrimination and Stigma Scale (DISC-12) was used to measure both experienced and anticipated discrimination (Brohan et al. Reference Brohan, Clement, Rose, Sartorius, Slade and Thornicroft2013). The DISC was administered by the interviewer by telephone. It consists of 22 items on negative, mental health-related experiences of discrimination (covering 21 specific life areas, plus one for ‘other’ experience) and four items concerning anticipated discrimination. Each item is scored on a 4-point scale from ‘not at all’ to ‘a lot’.
The Resource Generator-UK (RG-UK) was used to evaluate the participant's access to social resources, a method of measuring social capital (Webber & Huxley, Reference Webber and Huxley2007). Social capital is defined as available resources accessible to the person through trusting and reciprocal relationships within the social networks (Henderson et al. Reference Henderson, Corker, Hamilton, Williams, Pinfold, Rose, Webber, Evans-Lacko and Thornicroft2014). The RG-UK evaluates the capacity of participants to obtain access to several skills and resources within their social network within 1 week, if they needed it. The items are grouped into 4 subscales, each representing a domain of social capital to which an individual may have access: domestic resources, personal skills, expert advice and problem-solving resources. A higher score indicates higher possibility to access to social capital.
In the telephone survey, participants' main socio-demographic and clinical data (i.e., age, gender, ethnicity, clinical diagnosis and employment status) were collected. These items were included in the analysis due to having potential impact on participant's coping strategy.
Statistical analysis
Descriptive statistics were performed in order to describe the overall sample and non-parametric tests were employed to test the association between coping strategies and experience with the TTC programme. In order to test the association between the experience with TTC programme on the ‘educating’ and ‘challenging’ coping strategies, linear regression models were employed and adjusted for: age, gender, psychiatric diagnosis, working status, ethnicity, RG-UK score, anticipated and experienced discrimination. In order to adjust for possible regional effects, NHS mental health trusts were grouped into four categories (North of England; England Midlands and East; South of England; and London) (http://www.healthcheck.nhs.uk/interactive_map) and also included in the models.
All confounders were identified a priori by previous studies (Miller & Kaiser, Reference Miller and Kaiser2001; Corrigan & Watson, Reference Corrigan and Watson2002; Mendoza-Denton et al. Reference Mendoza-Denton, Page-Gould, Pietrzak, Levin and van Laar2006; Ilic et al. Reference Ilic, Reinecke, Bohner, Röttgers, Beblo, Driessen, Frommberger and Corrigan2012; Evans-Lacko et al. Reference Evans-Lacko, Corker, Williams, Henderson and Thornicroft2014a , Reference Evans-Lacko, Courtin, Fiorillo, Knapp, Luciano, Park, Brunn, Byford, Chevreul, Forsman, Gulacsi, Haro, Kennelly, Knappe, Lai, Lasalvia, Miret, O'Sullivan, Obradors-Tarragó, Rüsch, Sartorius, Svab, van Weeghel, Van Audenhove, Wahlbeck, Zlati, McDaid and Thornicroft b ).
An interaction term was also added to the regression models between the time-point (each year of the Viewpoint campaign) and the exposure to the TTC programme variable, in order to identify any effect modification of the association between ‘Challenging’ and ‘Educating’ strategies.
Results
Descriptive results
During the period 2011–2014, 3903 mental health service users were interviewed. Respondents were disproportionately female (62.2%, n = 2430), with a mean (s.d.) age of 44.3 (11.4) years, and unemployment was reported by almost half of the sample (49.3%; N = 1922). The most commonly reported diagnoses were mood disorders (depression, 29.8%, n = 1059; bipolar disorder, 20.7%, n = 734), followed by schizophrenia/schizoaffective disorders (17.2%, n = 610); anxiety disorders (12.1%, n = 431); personality disorders (9.3%, n = 329); and other mental disorders (11.0%, n = 389) (see Table 1).
* Missing data, N = 17.
We found a slightly higher reported use of the educating strategy (40.9%, n = 1596) compared with the challenging strategy (38.7%, n = 1513) (p < 0.001).
As regards service users' awareness or involvement in TTC, the proportion of people who actively participated in the campaign ranged from 2.3% in 2011 to 3.8% in 2014. However, there was an increase in the proportion stating they had seen at least some publicity about TTC, from 17% in 2011 to 29.1% in 2014.
As regards the challenging strategy, respondents participating in programme activities 2011–2014 reported using it more frequently than people who had never heard about TTC (57.3% v. 37.0%; p < 0.001) as well as compared with people who had only seen some publicity (57.3% v. 41.2%; p < 0.001) (Table 2).
One-way ANOVA, with Bonferroni corrections.
a Having never heard about TTC v. Having participating in TTC, p < 0.001.
b Having seen some publicity v. Having participating in TTC, p < 0.001.
c Having never heard about TTC v. Having seen some publicity of TTC, p < 0.001.
For the educating coping strategy, mental health users having seen some publicity of TTC reported a higher endorsement of the strategy compared with those actively involved in the campaign (2.29 ± 0.73 v. 1.74 ± 0.79, p < 0.001). Respondents not aware of TTC also endorsed this strategy more frequently compared with people participating in some programme activities (2.34 ± 0.70 v. 1.74 ± 0.79, p < 0.001) (Table 2).
Association between TTC and coping strategies
We found that having actively participated in the campaign activities represented a good predictor of endorsing the challenging coping strategy (OR = 0.74, CI: 0.29–1.19; p < 0.05), adjusted for the impact of the year of the campaign, the geographical region and for the other socio-demographic confounding variables. Moreover, just having seen some publicity had a slight positive impact on endorsement of the challenging strategy, but it did not reach the level of statistical significance (see Table 3). Interestingly, we found that each psychiatric diagnosis had a different impact on the endorsement of the challenging coping strategy. In particular, people with depressive (OR = 0.20, CI: 0.04–0.36; p < 0.05) or personality disorders (OR = 0.23, CI: 0.04–0.43; p < 0.05) had a slightly higher probability of adopting such a strategy. Moreover, female participants (OR = 0.09, CI: 0.00–0.19; p < 0.05) and people with higher resources at the RG-UK scale (OR = 0.02, CI: 0.02–0.03; p < 0.05) were more prone to adopt the challenging strategy. Results of the multivariate multiple regression models are shown in Table 3.
*Significance level set at p < 0.005, all models adjusted for region, gender age, working status, ethnicity.
Wald test, educating: impact of TTC* year of the campaign, p < 0.001.
Wald test, challenging: impact of TTC* year of the campaign, p < 0.005.
As regards the educating coping strategy, mental health users actively participating in the programme's activities scored lower on the educating coping subscale (OR = −0.72, CI:−0.88 to −0.55; p < 0.05), also adjusting for confounding variables as the year of the Viewpoint survey. The clinical diagnosis seemed to have an impact on the endorsement of educating coping strategy, and people with a diagnosis of schizophrenia/schizoaffective disorders showed a higher probability of adopting such a strategy (OR = 0.1, CI: 0.01–0.22; p < 0.05). Interestingly, people reporting higher levels of anticipated discrimination were more likely to educate others on mental health topics (OR = 0.002, CI: 0.001–0.002; p < 0.05) (Table 3).
Discussion
Although there are several anti-stigma programmes ongoing in different countries, these have not to date explored the possible relationship between level of participation in such programmes and endorsement of coping strategies by service users. This study represents the first effort in Europe to test the possible role of an anti-stigma campaign as one of the potential predictors of mental health service users' ‘challenging’ and ‘educating’ coping strategies.
The hypothesis of the positive association between active involvements in TTC activities on two selected coping strategies was partially confirmed by our results. In particular, mental health service users actively participating in the anti-stigma project report that, they challenge stigma more than those not aware of TTC. Such a finding is consistent with the characteristics of TTC, which features contact-based activities between mental health users and members of the general population (Henderson & Thornicroft, Reference Henderson and Thornicroft2009; Henderson et al. Reference Henderson, Evans-Lacko and Thornicroft2013). On the other hand, longitudinal studies are needed in order to evaluate the long-term endorsement of the challenging strategy, beyond the duration of the anti-stigma campaign activity, which represents the ideal environment to apply it (Sartorius, Reference Sartorius2010).
Moreover, possible explanatory variables having an impact on challenging coping strategy were identified, as the role of female gender and of social capital. In particular, as regards gender, our data are in line with the results of the ‘Like Minds, Like Mine’ programme, which found that women were more likely than men to say they had coped with stigma and discrimination (Ministry of Health, New Zealand, 2011). Moreover, we found that social capital has a positive impact on the endorsement of the challenging coping strategy. This positive impact of social capital is in line with recent studies in the field of stigma showing that social capital is related with empowerment, impacting also on self-stigma (Brohan et al. Reference Brohan, Elgie, Sartorius and Thornicroft2010, Reference Brohan, Gauci, Sartorius and Thornicroft2011; Lanfredi et al. Reference Lanfredi, Zoppei, Ferrari, Bonetto, Van Bortel, Thornicroft, Knifton, Quinn, Rossi and Lasalvia2015; Corker et al. Reference Corker, Brown and Henderson2016).
On the other hand, our results did not confirm the hypothesis that participating in the programme activities is associated with more use of the educating coping strategy. To date, the total sample of mental health users interviewed reported adopting the educating strategy more frequently than the challenging one. This general trend in the sample may have reduced the possibility to evaluate the potential predictive role of the participation in the TTC programme on the adoption of such strategy. This finding deserves further study, considering that contact-based education strategies have been found to be more effective than protest for overcoming stigma in the adult population, while for adolescents education strategy seems more effective (Corrigan et al. Reference Corrigan, Morris, Michaels, Rafacz and Rüsch2012).
Moreover, we searched for the possible explanatory role of discrimination on coping strategies. It seems that the relationship between coping strategies and anticipated discrimination is very complex, considering that Brain et al. (Reference Brain, Sameby, Allerby, Quinlan, Joas, Lindström, Burns and Waern2014) found that anticipated discrimination was inversely associated with coping strategies. Such association was not confirmed in our study. A preliminary explanation could be due to the fact that some mental health users reporting anticipated discrimination want to take an action to prevent it, and so discrimination itself represents a good predictor for endorsing such coping strategies. Of course, this suggestion is tentative and future confirmatory studies are needed in order to disentangle and deepen the knowledge on the causal relationship between discrimination and coping responses.
Another interesting result is related to the increasing rate of mental health users stating they had ‘seen some publicity from the TTC programme’. It seems that since the start of the programme, mental health services' users are becoming more aware of TTC, findings in line with figures based on the social marketing campaign of the TTC (Evans-Lacko et al. Reference Evans-Lacko, Malcolm, West, Rose, London, Rüsch, Little, Henderson and Thornicroft2013).
The educating and challenging strategies were chosen as focus of the present study, as these strategies are related to the aims of the TTC programme (Henderson et al. Reference Henderson, Evans-Lacko and Thornicroft2013). In particular, the main feature of the TTC campaign activities was to invite people with mental disorders to participate in various sporting activity (i.e., ‘Get Moving!’) or in discussions on their diagnosis (e.g., ‘Living Libraries’) (London & Evans-Lacko, Reference London and Evans-Lacko2010). Taking this into account, the study focussed on the possible impact of the TTC activities on these two specific coping strategies. This methodological choice also avoided further increasing the length of the interview and the participants' burden in taking part.
In the present study, a cross-sectional design was adopted. This methodological choice could have limited our findings, considering that coping strategies are the results of a dynamic process (Hinshaw, Reference Hinshaw2007). Moreover, we were not able to detect to which extent the coping strategies are directly associated with exposure to the programme. This is due to the fact that the relevant questions were added in 2011, while the survey was launched in 2008. It could be that service users – already used to challenging stigma and educating others – were more likely to get involved in TTC. We addressed this limitation adjusting our regression analysis according to the years of the campaign and to the relevant interaction term.
Finally, a selection bias in respondents could have limited the generalisability of the present findings. It could be that those experiencing higher levels of discrimination were more likely to take part of the survey and were thus overrepresented. In fact, in our sample we found that people reporting higher levels of anticipated and experienced discrimination were more prone to adopt the challenging strategies. This could in part be due to them having more opportunities to do so.
The TTC anti-stigma programme represents one of the major efforts in England to end mental health stigma and discrimination. Evidence is encouraging on the positive relationship between participating in the activities of the TTC programme and using of challenging coping strategy. Such results shed light on the possible way forward in the field of fighting and overcoming stigma, although some gaps need to be filled in. To improve the research evidence base, a higher number of service users will need to be involved in the campaign activities, and the evaluation should have a longitudinal design. A possible solution could be represented by the promotion of further local activities led by service users and carers' as well as all others stakeholders' associations and by the more active involvement of mental health services (Fiorillo et al. Reference Fiorillo, Luciano, Del Vecchio, Sampogna, Obradors-Tarragó and Maj2013; Copeland et al. Reference Copeland, Thornicroft, Bird, Bowis and Slade2014; Forsman et al. Reference Forsman, Wahlbeck, Aarø, Alonso, Barry, Brunn, Cardoso, Cattan, de Girolamo, Eberhard-Gran, Evans-Lacko, Fiorillo, Hansson, Haro, Hazo, Hegerl, Katschnig, Knappe, Luciano, Miret, Nordentoft, Obradors-Tarragó, Pilgrim, Ruud, Salize, Stewart-Brown, Tómasson, van der Feltz-Cornelis, Ventus, Vuori and Värnik2015; Wykes et al. Reference Wykes, Haro, Belli, Obradors-Tarragó, Arango, Ayuso-Mateos, Bitter, Brunn, Chevreul, Demotes-Mainard, Elfeddali, Evans-Lacko, Fiorillo, Forsman, Hazo, Kuepper, Knappe, Leboyer, Lewis, Linszen, Luciano, Maj, McDaid, Miret, Papp, Park, Schumann, Thornicroft, van der Feltz-Cornelis, van Os, Wahlbeck, Walker-Tilley and Wittchen2015).
Acknowledgements
We are grateful for collaboration on the evaluation by: Sue Baker, Paul Farmer, and Paul Corry. During Phase 1 of TTC GT, DR and CH were funded in relation to a National Institute for Health Research (NIHR) Applied Programme grant awarded to the South London and Maudsley NHS Foundation Trust (GT). CH, SEL and EC were supported during phases 1 and 2 by the grants to Time to Change from Big Lottery, the UK Department of Health and Comic Relief, and ER during phase 2. CH was also funded by grants from the NIHR, Maudsley Charity and Guy’s and St Thomas’s Charity. GT is supported by the National Institute for Health Research (NIHR) Collaboration for Leadership in Applied Health Research and Care South London at King’s College London Foundation Trust. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health. GT acknowledges financial support from the Department of Health via the National Institute for Health Research (NIHR) Biomedical Research Centre and Dementia Unit awarded to South London and Maudsley NHS Foundation Trust in partnership with King’s College London and King’s College Hospital NHS Foundation Trust. GT is supported by the European Union Seventh Framework Programme (FP7/2007-2013) Emerald project.
Financial Support
The Time to Change evaluation was funded by the UK Government Department of Health, Comic Relief and Big Lottery Fund.
Conflict of Interest
None.
Ethical Standard
The authors assert that all procedures contributing to this work comply with the ethical standards of the relevant national and institutional committees on human experimentation and with the Helsinki Declaration of 1975, as revised in 2008.
Availability of Data and Materials
The DISC measure is available subject to terms and conditions at http://www.kcl.ac.uk/ioppn/depts/hspr/research/ciemh/cmh/CMH-Measures.aspx. The Viewpoint dataset is not available. Data sharing would first require an application to the UK's Health Research Authority, which the research team does not have the capacity to do now that the Viewpoint survey has been discontinued.