Perceived helpfulness of treatment for generalized anxiety disorder: a World Mental Health Surveys report

Dan J Stein; Alan E Kazdin; Ayelet Meron Ruscio; Wai Tat Chiu; Nancy A Sampson; Hannah N Ziobrowski; Sergio Aguilar-Gaxiola; Ali Al-Hamzawi; Jordi Alonso; Yasmin Altwaijri; Ronny Bruffaerts; Brendan Bunting; Giovanni de Girolamo; Peter de Jonge; Louisa Degenhardt; Oye Gureje; Josep Maria Haro; Meredith G Harris; Aimee Karam; Elie G Karam; Viviane Kovess-Masfety; Sing Lee; Maria Elena Medina-Mora; Jacek Moskalewicz; Fernando Navarro-Mateu; Daisuke Nishi; José Posada-Villa; Kate M Scott; Maria Carmen Viana; Daniel V Vigo; Miguel Xavier; Zahari Zarkov; Ronald C Kessler; on behalf of the WHO World Mental Health Survey collaborators

doi:10.1186/s12888-021-03363-3

. 2021 Aug 9;21:392. doi: 10.1186/s12888-021-03363-3

Perceived helpfulness of treatment for generalized anxiety disorder: a World Mental Health Surveys report

Dan J Stein ^1,^✉, Alan E Kazdin ², Ayelet Meron Ruscio ³, Wai Tat Chiu ⁴, Nancy A Sampson ⁴, Hannah N Ziobrowski ⁴, Sergio Aguilar-Gaxiola ⁵, Ali Al-Hamzawi ⁶, Jordi Alonso ^7,^8,⁹, Yasmin Altwaijri ¹⁰, Ronny Bruffaerts ¹¹, Brendan Bunting ¹², Giovanni de Girolamo ¹³, Peter de Jonge ^14,¹⁵, Louisa Degenhardt ¹⁶, Oye Gureje ¹⁷, Josep Maria Haro ¹⁸, Meredith G Harris ^19,²⁰, Aimee Karam ²¹, Elie G Karam ^21,^22,²³, Viviane Kovess-Masfety ²⁴, Sing Lee ²⁵, Maria Elena Medina-Mora ²⁶, Jacek Moskalewicz ²⁷, Fernando Navarro-Mateu ²⁸, Daisuke Nishi ^29,³⁰, José Posada-Villa ³¹, Kate M Scott ³², Maria Carmen Viana ³³, Daniel V Vigo ^34,³⁵, Miguel Xavier ³⁶, Zahari Zarkov ³⁷, Ronald C Kessler ⁴; on behalf of the WHO World Mental Health Survey collaborators

¹Department of Psychiatry & Mental Health and South African Medical Council Research Unit on Risk and Resilience in Mental Disorders, University of Cape Town and Groote Schuur Hospital, Cape Town, South Africa

²Department of Psychology, Yale University, New Haven, CT USA

³Department of Psychology, University of Pennsylvania, Philadelphia, PA USA

⁴Department of Health Care Policy, Harvard Medical School, Boston, MA USA

⁵Center for Reducing Health Disparities, UC Davis Health System, Sacramento, California, USA

⁶College of Medicine, Al-Qadisiya University, Diwaniya governorate, Al Diwaniyah, Iraq

⁷Health Services Research Unit, IMIM-Hospital del Mar Medical Research Institute, Barcelona, Spain

⁸CIBER en Epidemiología y Salud Pública (CIBERESP), Madrid, Spain

⁹Pompeu Fabra University (UPF), Barcelona, Spain

¹⁰Epidemiology Section, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia

¹¹Universitair Psychiatrisch Centrum - Katholieke Universiteit Leuven (UPC-KUL), Campus Gasthuisberg, Leuven, Belgium

¹²School of Psychology, Ulster University, Londonderry, UK

¹³IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Brescia, Italy

¹⁴Department of Developmental Psychology, University of Groningen, Groningen, Netherlands

¹⁵Interdisciplinary Center Psychopathology and Emotion Regulation, University Medical Center Groningen, Groningen, Netherlands

¹⁶National Drug and Alcohol Research Centre, University of New South Wales, Sydney, Australia

¹⁷Department of Psychiatry, University College Hospital, Ibadan, Nigeria

¹⁸Parc Sanitari Sant Joan de Déu, CIBERSAM, Universitat de Barcelona, Sant Boi de Llobregat, Barcelona, Spain

¹⁹School of Public Health, The University of Queensland, Herston, QLD 4006 Australia

²⁰Queensland Centre for Mental Health Research, The Park Centre for Mental Health, Wacol, QLD 4072 Australia

²¹Institute for Development, Research, Advocacy & Applied Care (IDRAAC), Beirut, Lebanon

²²Department of Psychiatry and Clinical Psychology, St George Hospital University Medical Center, Beirut, Lebanon

²³Faculty of Medicine, Balamand University, Beirut, Lebanon

²⁴Ecole des Hautes Etudes en Santé Publique (EHESP), EA 4057, Paris Descartes University, Paris, France

²⁵Department of Psychiatry, Chinese University of Hong Kong, Tai Po, Hong Kong

²⁶National Institute of Psychiatry-Ramón de la Fuente Muñiz, Mexico City, Mexico

²⁷Institute of Psychiatry and Neurology, Warsaw, Poland

²⁸UDIF-SM, Servicio Murciano de Salud; IMIB-Arrixaca; CIBERESP-Murcia, Región de Murcia, Murcia, Spain

²⁹Department of Mental Health, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

³⁰National Center of Neurology and Psychiatry, Tokyo, Japan

³¹Colegio Mayor de Cundinamarca University, Faculty of Social Sciences, Bogota, Colombia

³²Department of Psychological Medicine, University of Otago, Dunedin, Otago New Zealand

³³Department of Social Medicine, Postgraduate Program in Public Health, Federal University of Espírito Santo, Vitoria, Brazil

³⁴Department of Psychiatry, University of British Columbia, Vancouver, BC Canada

³⁵Department of Global Health and Social Medicine, Harvard Medical School, Boston, MA USA

³⁶Lisbon Institute of Global Mental Health and Chronic Diseases Research Center (CEDOC), NOVA Medical School-Faculdade de Ciências Médicas, Universidade Nova de Lisboa, Lisbon, Portugal

³⁷Department of Mental Health, National Center of Public Health and Analyses, Sofia, Bulgaria

^✉

Corresponding author.

PMCID: PMC8351147 PMID: 34372811

Abstract

Background

Treatment guidelines for generalized anxiety disorder (GAD) are based on a relatively small number of randomized controlled trials and do not consider patient-centered perceptions of treatment helpfulness. We investigated the prevalence and predictors of patient-reported treatment helpfulness for DSM-5 GAD and its two main treatment pathways: encounter-level treatment helpfulness and persistence in help-seeking after prior unhelpful treatment.

Methods

Data came from community epidemiologic surveys in 23 countries in the WHO World Mental Health surveys. DSM-5 GAD was assessed with the fully structured WHO Composite International Diagnostic Interview Version 3.0. Respondents with a history of GAD were asked whether they ever received treatment and, if so, whether they ever considered this treatment helpful. Number of professionals seen before obtaining helpful treatment was also assessed. Parallel survival models estimated probability and predictors of a given treatment being perceived as helpful and of persisting in help-seeking after prior unhelpful treatment.

Results

The overall prevalence rate of GAD was 4.5%, with lower prevalence in low/middle-income countries (2.8%) than high-income countries (5.3%); 34.6% of respondents with lifetime GAD reported ever obtaining treatment for their GAD, with lower proportions in low/middle-income countries (19.2%) than high-income countries (38.4%); 3) 70% of those who received treatment perceived the treatment to be helpful, with prevalence comparable in low/middle-income countries and high-income countries. Survival analysis suggested that virtually all patients would have obtained helpful treatment if they had persisted in help-seeking with up to 10 professionals. However, we estimated that only 29.7% of patients would have persisted that long. Obtaining helpful treatment at the person-level was associated with treatment type, comorbid panic/agoraphobia, and childhood adversities, but most of these predictors were important because they predicted persistence rather than encounter-level treatment helpfulness.

Conclusions

The majority of individuals with GAD do not receive treatment. Most of those who receive treatment regard it as helpful, but receiving helpful treatment typically requires persistence in help-seeking. Future research should focus on ensuring that helpfulness is included as part of the evaluation. Clinicians need to emphasize the importance of persistence to patients beginning treatment.

Supplementary Information

The online version contains supplementary material available at 10.1186/s12888-021-03363-3.

Keywords: Generalized anxiety disorder, Pathways to treatment, Patient-centered outcomes, Treatment helpfulness

Background

Generalized Anxiety Disorder (GAD) encompasses a variety of symptoms including excessive worrying, restlessness, irritability, difficulties in concentration, and constantly feeling on edge. Among the anxiety disorders, GAD is perhaps the least well researched or understood in part because of multiple revisions of the diagnostic criteria, consideration of the diagnosis as a “wastebasket” category when other anxiety diagnoses could not made, and because worrying was assumed a part of everyday life and associated with minimal impairment. However, GAD is now known now to be a significant disorder with high prevalence and significant impairment and disability [1, 2]. Worldwide an estimated 3.7% of individuals will have GAD in their lifetime [1]. The role and quality of life impairments of GAD are comparable in magnitude to those of major depression and greater than those associated with substance abuse disorders [3].

Randomized controlled trials (RCTs) have identified effective pharmacological and psychosocial treatments [4–7]. However, results from RCTs do not necessarily translate into real-world settings and are largely restricted to high-income countries (HICs) with little global evaluation of the effects of treatment [8–10]. Moreover, RCTs have focused on symptom reduction as the critical and sometimes the sole outcome. Yet, symptom reduction does not necessarily equate with functional improvement, quality of life, or feelings on the part of the patient that they have been helped [11, 12].

Perceived helpfulness of treatment is a key construct that may capture whether patients achieve personally meaningful goals through treatment. Helpfulness is important in its own right, but also has a critical role in treatment in that perceived helpfulness relates directly to treatment adherence as well as to critical processes that span diverse forms psychotherapy (e.g., the therapeutic alliance, critical incidents during treatment, openness of the therapist) [13–16]. Helpfulness as an outcome of treatment has received little attention in GAD trials [17]. The extent to which helpfulness is achieved with treatment and whether this is achieved initially as the patient traverses different treatments remain to be evaluated. Such research might help identify unmet patient needs that can be targeted through policy and service responses [14, 18, 19]. Patient-centered research on perceived GAD treatment helpfulness may also inform treatment guidelines for GAD, which are currently based on a relatively small number of RCTs.

The likelihood of a help-seeking individual ever obtaining helpful treatment is a joint function of two treatment pathways: 1) the probability that a given treatment provider will be helpful, and 2) the probability that a patient will persist in help-seeking after prior unhelpful treatment encounters. Research on these processes for depression and posttraumatic stress disorder found that the majority of patients who persisted after previous unhelpful treatments eventually obtained helpful treatments, but that only a minority persisted in help-seeking after more than a few unsuccessful treatment encounters [20, 21]. It is unknown whether these patterns also are true for GAD. Decomposing treatment pathways for GAD would answer this question and might also reveal modifiable predictors of GAD treatment helpfulness and persistence that could be the focus of treatment quality improvement initiatives.

The present study evaluated the helpfulness of treatment encounters and predictors and pathways leading to helpfulness in national community epidemiological samples that included respondents with a history of GAD who sought treatment for their GAD. The data come from the World Mental Health (WMH) Survey Initiative [22]. This is a coordinated series of general population surveys under the auspices of the World Health Organization. Data were collected in 23 countries of varying income levels. This data set provides a unique opportunity to evaluate helpfulness internationally and to investigate predictors and pathways of perceived treatment response in countries varying in income levels.

Methods

Samples

The World Health Organization’s (WHO) World Mental Health (WMH) surveys are a coordinated set of community epidemiological surveys administered to probability samples of the non-institutionalized household population in countries throughout the world (https://www.hcp.med.harvard.edu/wmh/) [23]. Data for the current report came from 26 WMH surveys carried out in 23 countries – 9 in countries classified by the World Bank as low/middle-income (Brazil, Bulgaria [separate surveys carried out in 2002 and 2016], Colombia, Colombia [Medellin], Iraq, Lebanon, Mexico, and Peru) and 17 in countries classified as HICs (Argentina, Australia, Belgium, France, Germany, Israel, Italy, Japan, the Kingdom of Saudi Arabia, the Netherlands, New Zealand, Northern Ireland, Poland, Portugal, Spain, Spain [Murcia], and the United States). Response rates ranged from 45.9% (France) to 97.2% (Colombia [Medellin]) and averaged 67.4% across surveys (see eTable 1 for detailed survey characteristics).

The interview schedule was developed in English and translated into other languages using a standardized WHO translation, back-translation, and harmonization protocol [24]. Interviews were administered face-to-face in respondents’ homes after obtaining informed consent using procedures approved by local Institutional Review Boards. To reduce respondent burden, interviews were administered in two parts. Part I was administered to all respondents and assessed core DSM-IV mental disorders. Part II assessed additional disorders and correlates and was administered to all respondents who met lifetime criteria for any Part I disorder and a probability subsample of other Part I respondents [25].

Measures

Generalized anxiety disorder (GAD)

Lifetime history of GAD was assessed with the fully structured WHO Composite International Diagnostic Interview (CIDI) Version 3.0 [23]. In an evaluation carried out in conjunction with the US WMH survey [26], GAD diagnoses based on the CIDI had good concordance with diagnoses based on blinded clinical reassessments with the Structured Clinical Interview for DSM-IV (SCID) [27]. A clinical reappraisal study in other WMH surveys, although not evaluating GAD in isolation, found good concordance between diagnoses based on the CIDI and SCID for any 12-month anxiety disorder including GAD [28]. Consistent with previous studies that modified the CIDI GAD algorithm [1, 26, 29], we generated DSM-5 GAD diagnoses by removing the DSM-IV hierarchical exclusion of a GAD diagnosis when symptoms occur exclusively during a mood disorder [30]. Age of onset (AOO) of GAD was assessed using probing methods demonstrated to improve dating accuracy [31].

Perceived helpfulness of treatment for GAD

Respondents who met lifetime criteria for GAD were asked whether they had ever “talk [ed] to a medical doctor or other professional about their worry or anxiety” and, if so, how old they were the first time they did so. “Other professionals” were defined broadly to include “psychologists, counselors, spiritual advisors, herbalists, acupuncturists, and other healing professionals.” Respondents who had ever spoken to a professional about their GAD were asked whether they ever received treatment they “considered helpful or effective” (emphasis in original). If so, they were asked how many professionals they ever talked to about their worry or anxiety “up to and including the first time [they] ever got helpful treatment”. Respondents who said they never received helpful treatment were asked how many professionals they ever talked to about their worry or anxiety.

Predictors of obtaining helpful treatment for GAD

In addition to age of onset of GAD (continuous), we considered 5 classes of predictors of helpful treatment: Socio-demographic characteristics included sex, marital status (currently married, never married, or previously married) at the time of first treatment, and education (in quartiles defined by within-country distributions) at the time of first treatment. Lifetime comorbid conditions included other lifetime anxiety disorders (including panic disorder or agoraphobia with/ without panic disorder, post-traumatic stress disorder, specific phobia, and social phobia), major depressive disorder, broadly defined bipolar spectrum disorder [32], alcohol and/ or drug abuse, and alcohol and/ or drug dependence but not abuse. Comorbid conditions were restricted to disorders with an age-of-onset prior to the age at which the respondent first sought treatment for GAD. All comorbid conditions were assessed with the CIDI. Treatment type was defined as a cross-classification of (i) whether the respondent reported receiving medication, psychotherapy, or both, as of the age of first GAD treatment; and (ii) the types of treatment providers seen as of that age. Types of providers included mental health specialists (psychiatrist, psychiatric nurse, psychologist, psychiatric social worker, mental health counselor), primary care providers, human services providers (social worker or counselor in a social services agency, spiritual advisor), and complementary-alternative medicine (other type of healer or self-help group). Treatment timing included a continuous variable for length of delay in years between age of onset of GAD and age of initially seeking treatment, and a dichotomous measure for whether the respondent’s first attempt to seek treatment occurred before or after the year 2000. The year 2000 was the typical midpoint between the start of observations and survey field dates. Childhood adversities included retrospective reports of significant stressors experienced during childhood, including family dysfunction (physical or sexual abuse, neglect, parental mental disorder, parental substance use disorder, parental criminal behavior, and family violence) and other adversities (parental death, parental divorce, other loss of a parent, physical illness, and economic adversity).

Analysis methods

The sample was limited to respondents with a history of DSM-5 GAD treatment who sought treatment for the disorder at some time in their life. Cases were limited to those who first sought GAD treatment in 1990 or later to reduce the potential effects of recall bias. To investigate the two pathways of helpful treatment separately, we used discrete-event survival analysis to calculate the conditional and cumulative probabilities of: (i) obtaining helpful treatment after seeing between 1 and 10 professionals; and (ii) persisting in help-seeking after obtaining prior unhelpful treatment [33]. We followed respondents up through 10 professionals in the total sample and in HICs because this was the last number where at least n = 30 respondents received treatment. However, in low/middle-income countries (LMICs), we followed respondents only up through 3 professionals seen because this was the last number where at least n = 30 respondents received treatment.

We then carried out parallel survival analyses of the predictors of these two decomposed, encounter-level outcomes using standard discrete-time methods and a logistic link function [34], followed by a person-level model of overall probability of ever obtaining helpful treatment regardless of number of professionals seen (composite outcome). This allowed us to investigate predictors of obtaining helpful treatment at the person level and to investigate the extent to which these predictors were important because they predicted differential helpfulness at the encounter level, differential probability of persisting after earlier unhelpful treatments, or both.

We also investigated possible interactions of each significant person-level predictor with country income group and historical time (beginning treatment in 1990–1999 vs. 2000+) in an effort to examine the generalizability of the findings. Because the WMH sample design used weighting and clustering in all countries, all statistical analyses were carried out using the Taylor series linearization method [35], a design-based method implemented in the SAS 9.4 program [36]. Logistic regression coefficients and +/− 2 of their design-based standard errors were exponentiated to create odds-ratios (ORs) and 95% confidence intervals (CIs) (with odds ratios less than 1 indicating lower likelihood, and odds ratios greater than 1 indicating greater likelihood, of the relevant association). Significance of sets of coefficients was evaluated with Wald χ² tests based on design-corrected coefficient variance-covariance matrices. Statistical significance was evaluated using two-sided, design-based .05 level tests.

Results

GAD prevalence, treatment, and perceived helpfulness of treatment

Lifetime prevalence (SE) of GAD was 2.8% (0.1) in LMICs, 5.3% (0.1) in HICs, and 4.5% (0.1) across all WMH surveys (Table 1). Among respondents with lifetime GAD, approximately one-third reported ever obtaining GAD treatment (34.6% [0.8]) and 70.0% (1.4) of those who obtained GAD treatment perceived the treatment to be helpful. Respondents with GAD in LMICs were significantly less likely than those in HICs to obtain GAD treatment (19.2% vs. 38.4%; χ²₁ = 63.6, p < 0.001), but probability of treatment being perceived as helpful did not differ significantly by country income level (62.8% vs. 70.9%; χ²₁ = 2.7, p = 0.099).

Table 1.

Lifetime prevalence of DSM-5 generalized anxiety disorder (GAD), proportion of respondents with lifetime GAD who obtained treatment, and proportion of treated respondents who perceived treatment as helpful

	Total sample			Respondents with lifetime GAD			Respondents who obtained treatment for GAD
	Prevalence of lifetime GAD			Proportion who obtained treatment^a			Proportion who perceived treatment as helpful^b
	%	(SE)	(n)	%	(SE)	(n)	%	(SE)	(n)
I. Low/middle-income countries
Sao Paulo, Brazil	5.1	(0.4)	(5037)	23.6	(3.5)	(280)	71.4	(7.4)	(63)
Bulgaria	2.2	(0.2)	(6826)	16.8	(3.2)	(157)	69.4	(10.0)	(27)
Colombia	1.9	(0.3)	(4426)	15.8	(4.6)	(84)	45.0	(17.4)	(15)
Medellin, Colombia	3.8	(0.5)	(3261)	17.9	(3.4)	(127)	73.7	(9.8)	(31)
Iraq	5.0	(0.6)	(4332)	22.2	(5.5)	(220)	52.5	(13.8)	(33)
Lebanon	2.3	(0.3)	(2857)	12.4	(4.7)	(71)	38.1	(19.1)	(9)
Mexico	1.1	(0.2)	(5782)	8.5	(3.8)	(78)	28.4	(17.6)	(8)
Peru	1.0	(0.1)	(3930)	23.0	(8.3)	(40)	82.1	(8.5)	(10)
All	2.8	(0.1)	(36,451)	19.2	(1.8)	(1057)	62.8	(4.9)	(196)
χ²₇	242.3*			8.4			11.2
II. High-income countries
Argentina	5.2	(0.6)	(3927)	34.7	(6.0)	(224)	85.1	(6.0)	(70)
Australia	8.0	(0.4)	(8463)	49.0	(2.5)	(713)	76.7	(3.0)	(326)
Belgium	3.2	(0.8)	(1043)	35.6	(12.5)	(62)	33.9	(18.5)	(20)
France	6.0	(0.7)	(1436)	33.2	(4.4)	(159)	71.1	(7.7)	(62)
Germany	1.7	(0.4)	(1323)	34.2	(8.7)	(48)	80.5	(13.3)	(19)
Israel	4.4	(0.3)	(4859)	36.9	(3.4)	(216)	44.6	(5.9)	(76)
Italy	1.9	(0.3)	(1779)	24.3	(4.8)	(78)	89.1	(6.2)	(25)
Japan	2.6	(0.3)	(4129)	30.9	(4.8)	(105)	67.5	(10.2)	(30)
Netherlands	3.6	(0.4)	(1094)	46.4	(6.3)	(95)	88.3	(5.3)	(45)
New Zealand	7.9	(0.3)	(12,790)	41.2	(1.9)	(1084)	68.0	(2.8)	(411)
Northern Ireland	6.4	(0.4)	(4340)	39.6	(2.3)	(334)	70.2	(4.9)	(131)
Poland	0.9	(0.1)	(10,081)	37.8	(5.0)	(90)	73.7	(7.4)	(33)
Portugal	6.1	(0.5)	(3849)	41.3	(2.7)	(269)	73.4	(5.7)	(104)
Saudi Arabia	2.3	(0.4)	(3638)	27.5	(9.1)	(81)	56.7	(17.7)	(23)
Spain	1.9	(0.2)	(2121)	36.3	(5.0)	(114)	90.1	(3.5)	(41)
Murcia, Spain	7.0	(0.9)	(2621)	37.5	(4.6)	(193)	76.4	(9.4)	(80)
United States	7.8	(0.3)	(9282)	28.1	(2.3)	(752)	69.5	(3.2)	(205)
All	5.3	(0.1)	(76,775)	38.4	(0.9)	(4617)	70.9	(1.4)	(1701)
	%	(SE)	(n)	%	(SE)	(n)	%	(SE)	(n)
χ²₁₆	731.6*			53.7*			54.1*
III. Pooled countries
All countries	4.5	(0.1)	(113,226)	34.6	(0.8)	(5674)	70.0	(1.4)	(1897)
χ²₂₄	1276.3*			150.4*			67.0*
Low/middle-income countries vs. high-income countries
χ²₁	206.6*			63.6*			2.7

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Abbreviations. GAD generalized anxiety disorder; SE, standard error

*Significant at the .05 level, two-sided test

^aCases are based on three conditions: (i) Respondents obtained GAD treatment; (ii) Year of first GAD treatment ≥1990; and (iii) Age at onset of GAD ≤ Year of first GAD treatment

^bCases are based on four conditions: (i) Respondents obtained GAD treatment; (ii) Year of first GAD treatment ≥1990; and (iii) Age at onset of GAD ≤ Year of first GAD treatment; and (iv) Respondents obtained helpful treatment

Helpful GAD treatment across professionals seen

Across all countries, 26.7% (1.0) of respondents who received treatment said they were helped by the first professional they saw (Table 2, Part I). The conditional probability of obtaining helpful treatment from a second professional seen after an initial unhelpful treatment was 36.6%. Conditional probabilities of obtaining helpful treatment generally declined after subsequent professionals seen but projected cumulative probabilities of obtaining helpful treatment rose from 26.7% after the first professional seen to 53.5% among respondents who persisted in seeing a second professional and to 96.9% among those who persisted in seeing up to 10 professionals after prior unhelpful treatments (Table 2, Part II). These cumulative probabilities were broadly similar for LMICs and HICs up through three professionals seen (66.9% vs. 68.9%), after which the number of remaining respondents in LMICs became too small for analysis (eTable 2).

Table 2.

Conditional and cumulative probabilities of obtaining helpful treatment for generalized anxiety disorder after each professional seen, among respondents with lifetime DSM-5 generalized anxiety disorder who obtained treatment

	I. Conditional probabilities of obtaining helpful treatment			II. Cumulative probabilities of obtaining helpful treatment (n = 1897)
Number of professionals seen until the respondent obtained helpful treatment	%	(SE)	(n)	%	(SE)
1	26.7	(1.0)	(1897)	26.7	(1.0)
2	36.6	(1.7)	(1070)	53.5	(1.6)
3	33.1	(2.4)	(585)	68.9	(1.7)
4	29.0	(3.4)	(335)	77.9	(1.5)
5	25.2	(3.1)	(213)	83.5	(1.4)
6	33.1	(5.1)	(136)	89.0	(1.2)
7	16.4	(4.7)	(88)	90.8	(1.2)
8	16.6	(3.7)	(72)	92.3	(1.1)
9	3.5	(3.4)	(59)	92.6	(1.1)
10	57.9	(7.2)	(58)	96.9	(0.7)

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Abbreviations. SE standard error

Persistence with help-seeking for GAD following treatment failure

Across all countries, 77.3% (1.1) of respondents persisted in seeing a second professional after initial unhelpful GAD treatment (Table 3). This proportion was higher in HICs (79.6% [1.2]) than LMICs (55.8% [3.5]). Conditional probabilities of help-seeking persistence remained quite high (81.9–100.0%) in the total sample up through 10 professionals seen. Unlike the situation with cumulative probabilities of obtaining helpful treatment, which, by definition, either remains the same or rises as the number of professionals seen increases, the cumulative probability of help-seeking persistence either remains the same or decreases as the number of professionals seen increases. In the total sample, the cumulative probability of persistence through 10 professionals was 29.7%. We were able to compare respondents in LMICs to those in high income countries through four professionals seen, where the cumulative probability of persistence was lower in LMICs (43.2% [5.9]) than in high income countries (57.5% [2.5]) (eTable 3).

Table 3.

Conditional and cumulative probabilities of persistence in help-seeking after previous unhelpful treatment, among respondents with lifetime DSM-5 generalized anxiety disorder who obtained treatment

	I. Conditional probabilities of persistence in help-seeking			II. Cumulative probabilities of persistence in help-seeking (n = 1373)
Number of professionals seen after not being helped previously	%	(SE)	(n)	%	(SE)
2	77.3	(1.1)	(1373)	77.3	(1.1)
3	83.4	(1.5)	(696)	64.4	(1.9)
4	87.1	(1.8)	(385)	56.1	(2.3)
5	83.9	(2.1)	(248)	47.1	(2.4)
6	83.8	(2.8)	(157)	39.5	(2.6)
7	81.9	(4.9)	(102)	32.3	(2.9)
8	94.6	(1.9)	(77)	30.6	(2.9)
9	97.0	(0.4)	(61)	29.7	(2.9)
10	100.0	(0.0)	(58)	29.7	(2.9)

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Abbreviations. SE standard error

Predictors of obtaining helpful treatment for GAD

We examined predictors of each respondent ever obtaining helpful GAD treatment regardless of number of professionals seen (Model 1; Table 4), then examined predictors separately for the two pathways to helpful treatment: obtaining helpful treatment from a given professional (Model 2; Table 4) and persisting in help-seeking after prior unhelpful treatment (Model 3; Table 4). We focus on the significant predictors at the person-level (Model 1; Table 4) and examine how the results in the decomposed models help explain these person-level associations. Due to high comorbidity between disorders and the potential for multicollinearity, we evaluated associations with comorbid disorders in separate univariate and then multivariate models. Only comorbid disorders that significantly predicted obtaining helpful treatment in the multivariate models were included in Models 1–3 as individual predictors (eTable 4).

Table 4.

Multivariable analysis of predictors of obtaining helpful treatment (person-level composite outcome) and of the decomposed encounter-level outcomes of helpful treatment and persistence, among people with lifetime DSM-5 generalized anxiety disorder who obtained treatment

	Composite outcome				Decomposed outcomes
	Model 1: Person-level relative-odds of obtaining helpful treatment (regardless of the number of professionals seen)				Model 2: Encounter-level relative-odds of obtaining helpful treatment from a given professional (pooled across professionals seen)				Model 3: Encounter-level relative-odds of the respondent persisting in help-seeking after prior unhelpful treatment (pooled across all unhelpful treatments)
	Prevalence		Multivariate		Prevalence		Multivariate		Prevalence		Multivariate
	Mean/%	(SE)	OR	(95% CI)	Mean/%	(SE)	OR	(95% CI)	Mean/%	(SE)	OR	(95% CI)
Age of GAD onset (years)	29.4	(0.3)	1.01	(1.00–1.02)	28.4	(0.4)	1.02*	(1.01–1.02)	27.7	(0.4)	0.99	(0.98–1.00)
χ²₁	2.63				22.41*				1.48
Female	67.3	(1.2)	1.18	(0.90–1.54)	66.8	(1.6)	1.21*	(1.03–1.41)	66.2	(1.8)	1.08	(0.85–1.39)
χ²₁	1.47				5.51*				0.42
Marital Status
Never married	36.9	(1.2)	1.06	(0.80–1.42)	36.6	(1.5)	1.18*	(1.01–1.38)	36.2	(1.7)	0.85	(0.65–1.10)
Previously married	22.9	(1.2)	0.99	(0.71–1.36)	24.0	(1.6)	0.88	(0.73–1.06)	24.6	(1.8)	1.08	(0.80–1.46)
Currently married	40.2	(1.2)	1.00	–	39.4	(1.5)	1.00	–	39.2	(1.7)	1.00	–
χ²₂	0.21				9.66*				2.03
Education
Low	13.7	(0.8)	0.63*	(0.42–0.95)	15.1	(1.1)	0.62*	(0.48–0.80)	16.1	(1.4)	0.92	(0.66–1.28)
Low-average	23.7	(1.2)	0.79	(0.57–1.09)	23.3	(1.4)	0.95	(0.77–1.17)	23.2	(1.6)	0.86	(0.62–1.18)
High-average	31.9	(1.2)	0.80	(0.58–1.10)	30.6	(1.5)	0.96	(0.81–1.15)	30.0	(1.7)	0.80	(0.58–1.10)
Student	10.4	(0.8)	0.59*	(0.36–0.99)	12.0	(1.2)	0.81	(0.59–1.11)	12.7	(1.5)	0.62*	(0.39–0.99)
High	20.2	(0.9)	1.00	–	19.0	(1.1)	1.00	–	18.0	(1.2)	1.00	–
χ²₄	7.74				17.37*				4.43
Treatment delay (years)^a	6.4	(0.3)	0.99	(0.98–1.00)	6.1	(0.3)	1.01*	(1.00–1.02)	6.2	(0.4)	0.98*	(0.96–0.99)
χ²₁	1.95				4.24*				12.44*
Started GAD treatment > = 2000 (vs. 1990–1999)	52.6	(1.2)	0.78	(0.60–1.01)	45.5	(1.4)	1.22*	(1.06–1.40)	43.1	(1.5)	0.61*	(0.48–0.76)
χ²₁	3.66				7.25*				18.38*
Treatment type^b
Mental health specialist + psychotherapy	55.3	(1.2)	0.83	(0.62–1.12)	60.3	(1.6)	0.73*	(0.59–0.91)	61.9	(1.8)	1.33	(0.98–1.81)
Mental health specialist + medication	55.7	(1.4)	1.46*	(1.05–2.02)	65.8	(1.6)	0.76*	(0.62–0.93)	67.8	(1.8)	2.00*	(1.50–2.67)
General medical	74.1	(1.1)	0.88	(0.63–1.22)	79.4	(1.2)	0.60*	(0.50–0.72)	81.5	(1.3)	1.56*	(1.14–2.14)
Complementary/alternative medicine	20.4	(1.0)	1.38	(0.97–1.97)	27.9	(1.5)	0.73*	(0.63–0.84)	30.1	(1.7)	1.99*	(1.43–2.77)
Human services	16.6	(0.9)	1.00	–	21.0	(1.4)	1.00	–	22.6	(1.6)	1.00	–
χ²₄	12.27*				50.39*				32.32*
Exactly 2 or more of the above	67.5	(1.1)	1.30	(0.89–1.89)	77.7	(1.1)	1.01	(0.75–1.35)	80.1	(1.2)	1.49*	(1.03–2.15)
χ²₁	1.80				0.00				4.56*
χ²₅	27.34*				77.21*				131.57*
Comorbidity
Number of comorbid disorders^c	1.7	(0.0)	1.06	(0.92–1.21)	1.9	(0.0)	0.98	(0.91–1.06)	1.9	(0.0)	1.10	(0.98–1.24)
χ²₁	0.67				0.20				2.56
Panic disorder or agoraphobia with/without panic	19.5	(1.0)	1.79*	(1.22–2.62)	24.8	(1.7)	0.93	(0.78–1.12)	25.8	(1.9)	2.12*	(1.53–2.94)
χ²₁	8.89*				0.57				20.15*
Major depressive disorder	51.3	(1.3)	1.21	(0.91–1.61)	51.4	(1.4)	1.26*	(1.07–1.49)	50.6	(1.6)	0.91	(0.69–1.20)
χ²₁	1.64				7.83*				0.47
Bipolar disorder	10.9	(0.8)	1.40	(0.89–2.21)	12.9	(1.2)	1.18	(0.93–1.50)	13.3	(1.3)	1.15	(0.76–1.75)
χ²₁	2.12				1.77				0.44
χ²₄	24.46*				10.08*				42.86*
Childhood adversities
Family dysfunction^d	31.4	(1.1)	0.75*	(0.58–0.96)	31.8	(1.4)	0.93	(0.78–1.10)	32.4	(1.5)	0.73*	(0.57–0.93)
Other^e	18.0	(0.9)	1.47*	(1.09–1.99)	17.8	(1.1)	1.13	(0.95–1.34)	17.5	(1.2)	1.51*	(1.10–2.07)
χ²₂	9.73*				2.84				12.06*
Global χ²₂₁	88.45*				181.41*				260.66*

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Abbreviations: CI confidence interval; GAD generalized anxiety disorder; OR odds ratio; SE standard error

*Significant at .05 level, two-sided test

^aTreatment delay (years) = Age at first GAD treatment – Age at onset of GAD

^bTreatment providers: mental health specialists (psychiatrist, psychiatric nurse, psychologist, psychiatric social worker, mental health counselor), primary care providers, human services providers (social worker or counselor in a social services agency, spiritual advisor), and complementary/alternative medicine (other type of healer or self-help group)

^cComorbid disorders include: panic disorder or agoraphobia with/without panic disorder, post-traumatic stress disorder, specific phobia, social phobia, major depressive disorder, bipolar disorder, alcohol and/or drug abuse, and alcohol or drug dependence but not abuse

^dFamily dysfunction includes: physical abuse, sexual abuse, neglect, parental mental disorder, parental substance use disorder, parental criminal behavior, and family violence

^eOther childhood adversities include: parental death, parental divorce, other loss of a parent, physical illness, and economic adversity

At the person-level, significant predictors of obtaining helpful treatment were treatment type (χ²₄ = 12.3, p = 0.015), comorbid panic/agoraphobia (χ²₁ = 8.9, p = 0.003), and childhood adversities (χ²₂ = 9.7, p = 0.008). The association with treatment type was because respondents who received treatment from a mental health specialist in combination with medication had significantly increased relative-odds of obtaining helpful treatment than those who received treatment in the human services sector (the reference category; OR:1.46; 95% CI: 1.05, 2.02). Decomposition showed that this person-level association of treatment from a mental health specialist in combination with the outcome was due to lower relative-odds of encounter-level helpfulness (OR: 0.76; 95% CI: 0.62, 0.93), but higher relative-odds of treatment persistence (OR: 2.00; 95% CI: 1.50, 2.67). Comorbid panic/agoraphobia was associated at the person-level with having significantly increased relative-odds of obtaining helpful treatment (OR: 1.79; 95% CI: 1.22, 2.62) due to increased relative-odds of treatment persistence (OR: 2.12; 95% CI: 1.53, 2.94).

Childhood adversities were also important predictors of treatment helpfulness, but unexpectedly, the pattern of associations was different for the two classes of adversities. A history of family dysfunction was significantly associated with reduced relative-odds of obtaining helpful treatment at the person-level (OR: 0.75; 95% CI: 0.58, 0.96), whereas a history of other childhood adversities was significantly associated with increased relative-odds of obtaining helpful treatment (OR: 1.47; 95% CI: 1.09, 1.99). Decomposition showed that the person-level association of family dysfunction with the outcome was due to significantly reduced relative-odds of treatment persistence (OR: 0.73; 95% CI: 0.57, 0.93), whereas the person-level association other childhood adversities with the outcome was due to significantly increased relative-odds of treatment persistence (OR: 1.51; 95% CI: 1.10, 2.07). It is noteworthy that the zero- Pearson correlation between the two CA measures is too low (r = 0.23) to create an opposite-sign pattern as a methodological artifact. Consistent with this observation, the same opposite-sign pattern was also observed in models where only one of the two CA measures was included.

Although the omnibus χ² tests for treatment timing and treatment delay were not significant, there were significantly increased relative-odds of both predictors with significantly decreased relative-odds of with persistence in help-seeking after an initial unhelpful treatment, were found for both beginning treatment in more recent years (2000 or later) and longer treatment delays in obtaining helpful treatment from a given professional, resulting in nonsignificant associations at the person-level.

We found significant interactions of treatment type and childhood adversities with country income level (eTable 5). These interactions were due to the predictors being more strongly associated with person-level treatment helpfulness in LMICs than HICs (eTables 6 and 7), but the significant associations were based on such small numbers of cases that substantive interpretation is hazardous. Significant interactions were also found between treatment type and historical time (eTable 8). These were due to mental health specialist and psychotherapy treatment and general medical treatment both having increased relative-odds of person-level treatment helpfulness only during the years 1990–1999 and receiving treatment from 2+ types of professionals having increased relative-odds of person-level treatment helpfulness only during the years 2000+ (eTables 9 and 10). Again, though, these interactions were based on relatively small numbers of cases and should be interpreted with caution.

Discussion

The main findings of the study are as follows. First, only about one-third of people with GAD reported ever obtaining treatment, with a lower proportion in LMICs than HICs (19.2% vs. 38.4%). Second, 70% of those who received treatment perceived the treatment to be helpful. This did not vary by country income level. Third, persistence in help-seeking was required to obtain helpful treatment, as only about one-fourth of patients were helped by the first professional they saw and about half by the first two professionals. Projections from our survival models suggest that up to 10 professionals might be needed to have a 90% probability of being helped, but that only 29.7% of patients would persist that long in the face of repeated unhelpful treatment encounters. Fourth, only relatively modest predictors were found of obtaining helpful treatment at the person-level, most of which were important because they predicted persistence rather than encounter-level treatment helpfulness.

It is encouraging that the large majority (70.0%) of respondents with lifetime DSM-5 GAD who sought treatment eventually obtained treatment they considered helpful. This means that the majority of patients persisted up to 3–4 professions in the face of initial unhelpful treatment. This is a lower persistence rate than found in a parallel analysis of specific phobia [37], but a higher persistence rate than found in parallel analyses of patients with major depression [20] and PTSD [21], possibly because depressive and PTSD symptoms are more likely than anxiety symptoms to lead to discouragement in help-seeking. Even so, we estimated than only 22.7% of GAD patients would persist in help-seeking to a point where they had near certainty of receiving helpful treatment.

Our data on the predictors of helpfulness are useful in beginning to delineate pathways. Patients who received treatment from a mental health specialist in combination with medication had significantly increased relative-odds of obtaining helpful treatment at the person-level than those who received treatment in the human services sector. This was due to lower relative-odds of encounter-level helpfulness, but higher relative-odds of treatment persistence. Patients who receive medication in addition to seeing a mental health specialist may have been more severe than other patients, resulting in lower relative-odds of encounter-level helpfulness due to the severity of their illness, but also more motivation to persist in help-seeking because of that high severity. Likewise, panic/agoraphobia was also associated with having significantly increased relative-odds of obtaining helpful treatment at the person-level due to increased relative-odds of treatment persistence. These individuals may have more chronic and impairing courses of illness [38] which may motivate them to persist in help-seeking.

The relationship between childhood adversity and treatment helpfulness was less straightforward. Family dysfunction was associated with lower relative-odds of obtaining helpful treatment due to lower relative-odds of treatment persistence. In contrast, other childhood adversities were associated with greater relative-odds of obtaining helpful treatment due to increased relative-odds of treatment persistence. One possible explanation for this difference is that the family dysfunction category included violent and traumatic forms of adversity, whereas the other childhood adversities category did not [39]. If this finding is replicated in other studies, future research should focus on why traumatic childhood events are associated with lower persistence in help-seeking, which could inform treatment guidelines.

Important limitations of this study should be noted. First, there was limited information about the precise nature of the interventions that respondents received and no information about sequencing of treatments across types of providers. Moreover, the treatments were not randomized nor evaluated in relation to quality of delivery (treatment integrity) or compliance on the part of the patient (adherence). Consequently, the relation of critical dimensions of treatment to helpfulness could not be discerned. Second, the sample was limited to respondents with onset of GAD treatment after 1990. Recall may have been biased and influenced evaluations of the treatments and helpfulness [40]. It is unclear whether these limitations would lead to upward or downward bias in estimates of treatment effectiveness at the encounter level or patient level. Despite these limitations, to our knowledge this is the first study of perceived helpfulness of treatment of GAD. A strength of the study is including large sample representing multiple countries and with the ability to evaluate commonalities and differences among low and middle income and high- income countries.

RCTs are clearly required to determine the efficacy and effectiveness of GAD treatments [4–7]. Although our data do not fill this need, they are important because they address issues that RCTs cannot. Specifically, RCTs typically focus on short-term effects (e.g., 3 months), assess mainly symptomatic changes, and exclude many people who might have more complicated disorders, such as those with psychiatric comorbidities but who would benefit from treatment [8]. Our study, in comparison, looked at a broad and representative sample without these exclusionary criteria and included information on how patients view their treatment. We would encourage the assessment of treatment helpfulness in clinical trials because it is distinguishable from symptomatic change. One can readily conceive of patients showing similar or identical changes on standardized symptom measures but in fact profiting in different degrees from treatment in their everyday lives and hence in their views of how much they have been helped [41].

Our findings suggest that treatment guidelines should not only encourage evidence-based interventions, but also should emphasize the value of treatment persistence. Our data do not allow us to study new treatments from the same provider. The persistence we examined was across providers. It should be noted, though, that evidence is clear in showing that patients can also be helped by new treatments from the same provider [42]. Further work is needed to expand GAD care to address treatment motivations and expectations and to determine the extent to which interventions to improve GAD treatment quality and persistence can improve outcomes.

Supplementary Information

12888_2021_3363_MOESM1_ESM.docx^{(93.5KB, docx)}

Additional file 1: Table 1. WMH sample characteristics by World Bank income categories^a. Table 2. Conditional and cumulative probabilities of obtaining helpful treatment for generalized anxiety disorder after each professional seen, among respondents with lifetime DSM-5 generalized anxiety disorder who obtained treatment in low/middle-income and high-income countries. Table 3. Conditional and cumulative probabilities of persistence in help-seeking after previous unhelpful treatment, among respondents with lifetime DSM-5 generalized anxiety disorder who obtained treatment in low/middle-income and high-income countries. Table 4. Predictors of obtaining helpful treatment (person-level), among people with lifetime DSM-5 generalized anxiety disorder who obtained treatment. Table 5. Interactions between main effects and country income group to predict obtaining helpful treatment (person-level composite outcome) and the decomposed encounter-level outcomes of helpful treatment and persistence, among people with lifetime DSM-5 generalized anxiety disorder who obtained treatment. Table 6. (Low/middle-income countries): Predictors of obtaining helpful treatment (person-level composite outcome) and of the decomposed encounter-level outcomes of helpful treatment and persistence, among people with lifetime DSM-5 generalized anxiety disorder who obtained treatment. Table 7. (High-income countries): Predictors of obtaining helpful treatment (person-level composite outcome) and of the decomposed encounter-level outcomes of helpful treatment and persistence, among people with lifetime DSM-5 generalized anxiety disorder who obtained treatment. Table 8. Interactions between main effects and historical time to predict obtaining helpfulness of treatment (person-level composite outcome) and the decomposed encounter-level outcomes of helpful treatment and persistence, among people with lifetime DSM-5 generalized anxiety disorder who obtained treatment. Table 9. (Started GAD treatment in 2000 or later): Predictors of obtaining helpful treatment (person-level composite outcome) and of the decomposed encounter-level outcomes of helpful treatment and persistence, among people with lifetime DSM-5 generalized anxiety disorder who obtained treatment. Table 10. (Started GAD treatment 1990 to 1999): Predictors of obtaining helpful treatment (person-level composite outcome) and of the decomposed encounter-level outcomes of helpful treatment and persistence, among people with lifetime DSM-5 generalized anxiety disorder who obtained treatment.

Acknowledgements

The WHO World Mental Health Survey collaborators are Sergio Aguilar-Gaxiola, MD, PhD; Ali Al-Hamzawi, MD; Mohammed Salih Al-Kaisy, MD; Jordi Alonso, MD, PhD; Yasmin A. Altwaijri, PhD; Laura Helena Andrade, MD, PhD; Lukoye Atwoli, MD, PhD; Corina Benjet, PhD; Guilherme Borges, ScD; Evelyn J. Bromet, PhD; Ronny Bruffaerts, PhD; Brendan Bunting, PhD; Jose Miguel Caldas-de-Almeida, MD, PhD; Graça Cardoso, MD, PhD; Somnath Chatterji, MD; Alfredo H. Cia, MD; Louisa Degenhardt, PhD; Koen Demyttenaere, MD, PhD; Silvia Florescu, MD, PhD; Giovanni de Girolamo, MD; Oye Gureje, MD, DSc, FRCPsych; Josep Maria Haro, MD, PhD; Meredith G. Harris, PhD; Hristo Hinkov, MD, PhD; Chi-yi Hu, MD, PhD; Peter de Jonge, PhD; Aimee Nasser Karam, PhD; Elie G. Karam, MD; Norito Kawakami, MD, DMSc; Ronald C. Kessler, PhD; Andrzej Kiejna, MD, PhD; Viviane Kovess-Masfety, MD, PhD; Sing Lee, MBBS; Jean-Pierre Lepine, MD; John J. McGrath, MD, PhD; Maria Elena Medina-Mora, PhD; Zeina Mneimneh, PhD; Jacek Moskalewicz, PhD; Fernando Navarro-Mateu, MD, PhD; Marina Piazza, MPH, ScD; Jose Posada-Villa, MD; Kate M. Scott, PhD; Tim Slade, PhD; Juan Carlos Stagnaro, MD, PhD; Dan J. Stein, FRCPC, PhD; Margreet ten Have, PhD; Yolanda Torres, MPH, Dra.HC; Maria Carmen Viana, MD, PhD; Daniel V. Vigo, MD, DrPH; Harvey Whiteford, MBBS, PhD; David R. Williams, MPH, PhD; Bogdan Wojtyniak, ScD.

Abbreviations

CIDI: Composite International diagnostic interview
GAD: Generalized anxiety disorder
RCT: Randomized control trial
WHO: World health organization
WMH: World mental health

Authors’ contributions

Substantial contribution to the conception of the work: DJS, AEK, MGH, DVV, RCK made substantial contribution to the conception of the work, and AEK, NAS, DVV, RCK made substantial contribution to design of the work. DJS, SAG, AAH, JA, YA, RB, BB, GDG, PDJ, LD, OG, JMH, AK, EGK, VKM, SL, MEMM, JM, FNM, DN, JPV, KMS, MCV, MX, ZZ, RCK made substantial contribution to the acquisition of data. WTC, NAS, RCK made substantial contribution to data analysis, and all authors made substantial contribution to interpretation of data. DJS, AEK, AMR, NAS, HNZ, RCK drafted the work and all authors substantively revised the work. All authors approved the submitted version and agreed to both to be personally accountable for the author’s own contributions and to ensure that questions related to the accuracy or integrity of any part of the work, even ones in which the author was not personally involved, are appropriately investigated, resolved, and the resolution documented in the literature.

Funding

The World Health Organization World Mental Health (WMH) Survey Initiative is supported by the United States National Institute of Mental Health (NIMH; R01 MH070884), the John D. and Catherine T. MacArthur Foundation, the Pfizer Foundation, the United States Public Health Service (R13-MH066849, R01-MH069864, and R01 DA016558), the Fogarty International Center (FIRCA R03-TW006481), the Pan American Health Organization, Eli Lilly and Company, Ortho-McNeil Pharmaceutical Inc., GlaxoSmithKline, and Bristol-Myers Squibb. We thank the staff of the WMH Data Collection and Data Analysis Coordination Centres for assistance with instrumentation, fieldwork, and consultation on data analysis. None of the funders had any role in the design, analysis, interpretation of results, or preparation of this paper. The views and opinions expressed in this report are those of the authors and should not be construed to represent the views of the World Health Organization, other sponsoring organizations, agencies, or governments.

The Argentina survey -- Estudio Argentino de Epidemiología en Salud Mental (EASM) -- was supported by a grant from the Argentinian Ministry of Health (Ministerio de Salud de la Nación) - (Grant Number 2002–17270/13–5). The 2007 Australian National Survey of Mental Health and Wellbeing is funded by the Australian Government Department of Health and Ageing. The São Paulo Megacity Mental Health Survey is supported by the State of São Paulo Research Foundation (FAPESP) Thematic Project Grant 03/00204–3. The Bulgarian Epidemiological Study of common mental disorders EPIBUL is supported by the Ministry of Health and the National Center for Public Health Protection. EPIBUL 2, conducted in 2016–17, is supported by the Ministry of Health and European Economic Area Grants. The Colombian National Study of Mental Health (NSMH) is supported by the Ministry of Social Protection. The Mental Health Study Medellín – Colombia was carried out and supported jointly by the Center for Excellence on Research in Mental Health (CES University) and the Secretary of Health of Medellín. The ESEMeD project is funded by the European Commission (Contracts QLG5–1999-01042; SANCO 2004123, and EAHC 20081308), (the Piedmont Region (Italy)), Fondo de Investigación Sanitaria, Instituto de Salud Carlos III, Spain (FIS 00/0028), Ministerio de Ciencia y Tecnología, Spain (SAF 2000–158-CE), Generalitat de Catalunya (2017 SGR 452; 2014 SGR 748), Instituto de Salud Carlos III (CIBER CB06/02/0046, RETICS RD06/0011 REM-TAP), and other local agencies and by an unrestricted educational grant from GlaxoSmithKline. Implementation of the Iraq Mental Health Survey (IMHS) and data entry were carried out by the staff of the Iraqi MOH and MOP with direct support from the Iraqi IMHS team with funding from both the Japanese and European Funds through United Nations Development Group Iraq Trust Fund (UNDG ITF). The Israel National Health Survey is funded by the Ministry of Health with support from the Israel National Institute for Health Policy and Health Services Research and the National Insurance Institute of Israel. The World Mental Health Japan (WMHJ) Survey is supported by the Grant for Research on Psychiatric and Neurological Diseases and Mental Health (H13-SHOGAI-023, H14-TOKUBETSU-026, H16-KOKORO-013, H25-SEISHIN-IPPAN-006) from the Japan Ministry of Health, Labour and Welfare. The Lebanese Evaluation of the Burden of Ailments and Needs Of the Nation (L.E.B.A.N.O.N.) is supported by the Lebanese Ministry of Public Health, the WHO (Lebanon), National Institute of Health/Fogarty International Center (R03 TW006481–01), anonymous private donations to IDRAAC, Lebanon, and unrestricted grants from, Algorithm, AstraZeneca, Benta, Bella Pharma, Eli Lilly, Glaxo Smith Kline, Lundbeck, Novartis, OmniPharma, Pfizer, Phenicia, Servier, UPO. The Mexican National Comorbidity Survey (MNCS) is supported by The National Institute of Psychiatry Ramon de la Fuente (INPRFMDIES 4280) and by the National Council on Science and Technology (CONACyT-G30544- H), with supplemental support from the Pan American Health Organization (PAHO). Te Rau Hinengaro: The New Zealand Mental Health Survey (NZMHS) is supported by the New Zealand Ministry of Health, Alcohol Advisory Council, and the Health Research Council. The Northern Ireland Study of Mental Health was funded by the Health & Social Care Research & Development Division of the Public Health Agency. The Peruvian World Mental Health Study was funded by the National Institute of Health of the Ministry of Health of Peru. The Polish project Epidemiology of Mental Health and Access to Care –EZOP Project (PL 0256) was carried out by the Institute of Psychiatry and Neurology in Warsaw in consortium with Department of Psychiatry - Medical University in Wroclaw and National Institute of Public Health-National Institute of Hygiene in Warsaw and in partnership with Psykiatrist Institut Vinderen–Universitet, Oslo. The project was funded by the European Economic Area Financial Mechanism and the Norwegian Financial Mechanism. EZOP project was co-financed by the Polish Ministry of Health. The Portuguese Mental Health Study was carried out by the Department of Mental Health, Faculty of Medical Sciences, NOVA University of Lisbon, with collaboration of the Portuguese Catholic University, and was funded by Champalimaud Foundation, Gulbenkian Foundation, Foundation for Science and Technology (FCT) and Ministry of Health. The Saudi National Mental Health Survey (SNMHS) is conducted by the King Salman Center for Disability Research. It is funded by Saudi Basic Industries Corporation (SABIC), King Abdulaziz City for Science and Technology (KACST), Ministry of Health (Saudi Arabia), and King Saud University. Funding in-kind was provided by King Faisal Specialist Hospital and Research Center, and the Ministry of Economy and Planning, General Authority for Statistics. The Psychiatric Enquiry to General Population in Southeast Spain – Murcia (PEGASUS-Murcia) Project has been financed by the Regional Health Authorities of Murcia (Servicio Murciano de Salud and Consejería de Sanidad y Política Social) and Fundación para la Formación e Investigación Sanitarias (FFIS) of Murcia. The US National Comorbidity Survey Replication (NCS-R) is supported by the National Institute of Mental Health (NIMH; U01-MH60220) with supplemental support from the National Institute of Drug Abuse (NIDA), the Substance Abuse and Mental Health Services Administration (SAMHSA), the Robert Wood Johnson Foundation (RWJF; Grant 044708), and the John W. Alden Trust.

A complete list of all within-country and cross-national WMH publications can be found at http://www.hcp.med.harvard.edu/wmh/.

Availability of data and materials

Access to the cross-national World Mental Health (WMH) data is governed by the organizations funding and responsible for survey data collection in each country. These organizations made data available to the WMH consortium through restricted data sharing agreements that do not allow us to release the data to third parties. The exception is that the U.S. data are available for secondary analysis via the Inter-University Consortium for Political and Social Research (ICPSR), http://www.icpsr.umich.edu/icpsrweb/ICPSR/series/00527.

Declarations

Ethics approval and consent to participate

The study protocol was approved by all local institutional review boards. Written or verbal informed consent was obtained in a manner consistent with the regulations of each country. Details of the ethics committees for the WMH surveys can be viewed at this link: http://www.hcp.med.harvard.edu/wmh/ftpdir/WMH_Ethics_approval.pdf. They are:

Bioethics Committee, School of Medicine, University of Buenos Aires (Argentina); the authority of Census and Statistics Act, 1905 (Australia); Ethics Committee of the Institute of Public

Health (Federal Public Service Health, Food Chain Safety, and Environment) (Belgium); Research and Ethics Committee of the School of Medicine, University of Sao Paulo (Brazil);

Deputy Minister and head of the Executive Committee of the National Psychiatric Program

(Bulgaria); Ethical committee of the National Center of Public Health and Analyses

(Bulgaria); Ethics Committee for the FES Social Foundation (Colombia); Comité Institucional de Ética Universidad CES (Colombia-Medellin); Committee of the CNIL - Commission Nationale Informatique et Libertés (France): Germany Ethics Committee of the University of Leipzig (Germany); Ethics Scientific Committee of the Ministry of Health Iraq (Iraq); Human Subjects Committee for survey and field procedures in Eitanim-Kfar Shaul Hospital (Israel); Italy Italian National Institute of Health (Italy); National Center of Neurology and Psychiatry; Okayama University School of Medicine; Nagasaki University School of Medicine; Keio University School of Medicine; Jichi University School of Medicine; Juntendo University School of Medicine; Yamagata University School of Medicine (Japan); University of Balamand Faculty of Medicine Institutional Review Board (Lebanon); Ethics committee in research of the National Institute of Psychiatry Ramon de la Fuente Muñiz (Mexico); Ethics Committee of the Netherlands Institute of Mental Health and Addiction (Netherlands); New Zealand Health Ethics Committees (New Zealand); University of Ulster Ethics Committee (Northern Ireland); Peru National Institute of Health Peru (Peru); Komisja Bioetyczna (Bioethical Committee) of Instytut Psychiatrii i Neurologi (Poland); Ethics Committee, Faculdade de Ciencias Médicas, Universidade Nova (Portugal); Office of Research Affairs at King Faisal Specialist Hospital and Research Center (Saudia Arabia); Ethical Committee of Sant Joan de Deu Serveis de Salut Mental and Ethical Committee of IMIMHospital del Mar Medical Research Institute (Spain-Murcia); The Clinical Research Ethics Committee of the University Hospital Virgen de la Arrixaca of Murcia (Spain); Human Subjects Committees of the Institute for Social Research at the University of Michigan and of Harvard Medical School (USA)

Consent for publication

Not applicable.

Competing interests

In the past 3 years, RCK reports being a consultant for Datastat, Inc., RallyPoint Networks, Inc., Sage Pharmaceuticals, and Takeda. FNM reports non-financial support from Otsuka outside and not related to the submitted work. In the past 3 years LD has received untied educational grant funding from Indivior and Seqirus, not related to the submitted work. DJS has received research grants and/or honoraria from Lundbeck, Johnson & Johnson, Servier and Takeda. The remaining authors declare that they have no competing interests.

Footnotes

Publisher’s Note

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

Contributor Information

Dan J. Stein, Email: dan.stein@uct.ac.za

on behalf of the WHO World Mental Health Survey collaborators:

Sergio Aguilar-Gaxiola, Ali Al-Hamzawi, Mohammed Salih Al-Kaisy, Jordi Alonso, Yasmin A. Altwaijri, Laura Helena Andrade, Lukoye Atwoli, Corina Benjet, Guilherme Borges, Evelyn J. Bromet, Ronny Bruffaerts, Brendan Bunting, Jose Miguel Caldas-de-Almeida, Graça Cardoso, Somnath Chatterji, Alfredo H. Cia, Louisa Degenhardt, Koen Demyttenaere, Silvia Florescu, Giovanni de Girolamo, Oye Gureje, Josep Maria Haro, Meredith G. Harris, Hristo Hinkov, Chi-yi Hu, Peter de Jonge, Aimee Nasser Karam, Elie G. Karam, Norito Kawakami, Ronald C. Kessler, Andrzej Kiejna, Viviane Kovess-Masfety, Sing Lee, Jean-Pierre Lepine, John J. McGrath, Maria Elena Medina-Mora, Zeina Mneimneh, Jacek Moskalewicz, Fernando Navarro-Mateu, Marina Piazza, Jose Posada-Villa, Kate M. Scott, Tim Slade, Juan Carlos Stagnaro, Dan J. Stein, Margreet ten Have, Yolanda Torres, Maria Carmen Viana, Daniel V. Vigo, Harvey Whiteford, David R. Williams, and Bogdan Wojtyniak

References

1.Ruscio AM, Hallion LS, Lim CCW, Aguilar-Gaxiola S, Al-Hamzawi A, Alonso J, et al. Cross-sectional comparison of the epidemiology of DSM-5 generalized anxiety disorder across the globe. JAMA Psychiatry. 2017;74(5):465–475. doi: 10.1001/jamapsychiatry.2017.0056. [DOI] [PMC free article] [PubMed] [Google Scholar]
2.Alonso J, Petukhova M, Vilagut G, Chatterji S, Heeringa S, Üstün TB, et al. Days out of role due to common physical and mental conditions: results from the WHO world mental health surveys. Mol Psychiatry. 2011;16(12):1234–46. 10.1038/mp.2010.101. [DOI] [PMC free article] [PubMed]
3.Hoffman DL, Dukes EM, Wittchen HU. Human and economic burden of generalized anxiety disorder. Depress Anxiety. 2008;25(1):72–90. doi: 10.1002/da.20257. [DOI] [PubMed] [Google Scholar]
4.Carl E, Witcraft SM, Kauffman BY, Gillespie EM, Becker ES, Cuijpers P, et al. Psychological and pharmacological treatments for generalized anxiety disorder (GAD): a meta-analysis of randomized controlled trials. Cogn Behav Ther. 2020;49(1):1–21. 10.1080/16506073.2018.1560358. [DOI] [PMC free article] [PubMed]
5.Mitte K. Meta-analysis of cognitive-behavioral treatments for generalized anxiety disorder: a comparison with pharmacotherapy. Psychol Bull. 2005;131(5):785–795. doi: 10.1037/0033-2909.131.5.785. [DOI] [PubMed] [Google Scholar]
6.Robichaud M, Koerner N, Dugas MJ. Cognitive behavioral treatment for generalized anxiety disorder: from science to practice: Routledge; 2019. 10.4324/9781315709741.
7.Stein DJ. Evidence-based treatment of anxiety disorders. Int J Psychiatry Clin Pract. 2006;10(sup1):16–21. [DOI] [PubMed]
8.Hoertel N, Le Strat Y, Blanco C, Lavaud P, Dubertret C. Generalizability of clinical trial results for generalized anxiety disorder to community samples. Depress Anxiety. 2012;29(7):614–620. doi: 10.1002/da.21937. [DOI] [PubMed] [Google Scholar]
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17.Alang SM, McAlpine DD. Pathways to mental health services and perceptions about the effectiveness of treatment. Soc Ment Health. 2019;9(3):388–407. doi: 10.1177/2156869318802341. [DOI] [Google Scholar]
18.Cuijpers P. Targets and outcomes of psychotherapies for mental disorders: an overview. World Psychiatry. 2019;18(3):276–285. doi: 10.1002/wps.20661. [DOI] [PMC free article] [PubMed] [Google Scholar]
19.Sharma T, Bamford M, Dodman D. Person-centred care: an overview of reviews. Contemp Nurse. 2015;51(2–3):107–120. doi: 10.1080/10376178.2016.1150192. [DOI] [PubMed] [Google Scholar]
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21.Stein DJ, Harris MG, Vigo DV, Tat Chiu W, Sampson N, Alonso J, et al. Perceived helpfulness of treatment for posttraumatic stress disorder: findings from the world mental health surveys. Depress Anxiety. 2020;37(10):972–94. 10.1002/da.23076. [DOI] [PMC free article] [PubMed]
22.Kessler RC, Ustun TB. The WHO mental health surveys. Global perspectives on the epidemiology of mental disorders. Cambridge, England: Cambridge University Press; 2008. [Google Scholar]
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24.Harkness J, Pennell B, Villar A, Gebler N, Aguilar-Gaxiola S, Bilgen I. Translation procedures and translation assessment in the world mental health survey initiative. In: Kessler R, Üstün T, editors. The WHO world mental health surveys: global perspectives on the epidemiology of mental disorders. New York, NY: Cambridge University Press; 2008. pp. 91–113. [Google Scholar]
25.Heeringa S, Wells J, Hubbard F, Mneimneh Z, Chiu W, Sampson N, et al. Sample designs and sampling procedures. In: Kessler R, Üstün T, et al., editors. The WHO world mental health surveys: global perspectives on the epidemiology of mental disorders. New York, NY: Cambridge University Press; 2008. pp. 14–32. [Google Scholar]
26.Ruscio AM, Lane M, Roy-Byrne P, Stang PE, Stein DJ, Wittchen H-U, et al. Should excessive worry be required for a diagnosis of generalized anxiety disorder? Results from the US National Comorbidity Survey Replication. Psychol Med. 2005;35(12):1761–1772. doi: 10.1017/S0033291705005908. [DOI] [PMC free article] [PubMed] [Google Scholar]
27.Spitzer M, Robert L, Gibbon M, Williams J. Structured clinical interview for DSM-IV-TR axis I disorders, research version, non-patient edition (SCID-I/NP) New York: Biometrics Research, New York State Psychiatric Institute; 2002. [Google Scholar]
28.Haro JM, Arbabzadeh-Bouchez S, Brugha TS, De Girolamo G, Guyer ME, Jin R, et al. Concordance of the composite international diagnostic interview version 3.0 (CIDI 3.0) with standardized clinical assessments in the WHO world mental health surveys. Int J Methods Psychiatr Res. 2006;15(4):167–180. doi: 10.1002/mpr.196. [DOI] [PMC free article] [PubMed] [Google Scholar]
29.Ruscio AM, Chiu WT, Roy-Byrne P, Stang PE, Stein DJ, Wittchen HU, et al. Broadening the definition of generalized anxiety disorder: effects on prevalence and associations with other disorders in the National Comorbidity Survey Replication. J Anxiety Disord. 2007;21(5):662–76. 10.1016/j.janxdis.2006.10.004. [DOI] [PMC free article] [PubMed]
30.American Psychiatric Association . Diagnostic and statistical manual of mental disorders (5th ed) Washington, DC: American Psychiatric Press; 2013. [Google Scholar]
31.Knäuper B, Cannell CF, Schwarz N, Bruce ML, Kessler RC. Improving accuracy of major depression age-of-onset reports in the US National Comorbidity Survey. Int J Methods Psychiatr Res. 1999;8(1):39–48. doi: 10.1002/mpr.55. [DOI] [Google Scholar]
32.Merikangas KR, Jin R, He JP, Kessler RC, Lee S, Sampson NA, et al. Prevalence and correlates of bipolar spectrum disorder in the world mental health survey initiative. Arch Gen Psychiatry. 2011;68(3):241–51. 10.1001/archgenpsychiatry.2011.12. [DOI] [PMC free article] [PubMed]
33.Halli SS, Rao KV. Advanced techniques of population analysis. Springer Science & Business Media: Boston, MA; 2013. [Google Scholar]
34.Willett JB, Singer JD. Investigating onset, cessation, relapse, and recovery: why you should, and how you can, use discrete-time survival analysis to examine event occurrence. J Conult Clin Psychol. 1993;61(6):952–965. doi: 10.1037/0022-006X.61.6.952. [DOI] [PubMed] [Google Scholar]
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36.SAS/ STAT . 14.3 software version 9.4 [computer program] Cary, NC: SAS Institute Inc; 2016. [Google Scholar]
37.de Vries YA, Harris MG, Vigo D, Chiu WT, Sampson NA, Al-Hamzawi A, et al. Perceived helpfulness of treatment for specific phobia: findings from the world mental health surveys. J Affect Disord. 2021;288:199–209. doi: 10.1016/j.jad.2021.04.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
38.Bruce SE, Yonkers KA, Otto MW, Eisen JL, Weisberg RB, Pagano M, et al. Influence of psychiatric comorbidity on recovery and recurrence in generalized anxiety disorder, social phobia, and panic disorder: a 12-year prospective study. Am J Psychiatry. 2005;162(6):1179–87. 10.1176/appi.ajp.162.6.1179. [DOI] [PMC free article] [PubMed]
39.Kessler RC, McLaughlin KA, Green JG, Gruber MJ, Sampson NA, Zaslavsky AM, et al. Childhood adversities and adult psychopathology in the WHO world mental health surveys. Br J Psychiatry. 2010;197(5):378–385. doi: 10.1192/bjp.bp.110.080499. [DOI] [PMC free article] [PubMed] [Google Scholar]
40.Zlomuzica A, Dere D, Machulska A, Adolph D, Dere E, Margraf J. Episodic memories in anxiety disorders: clinical implications. Front Behav Neurosci. 2014;8:131. doi: 10.3389/fnbeh.2014.00131. [DOI] [PMC free article] [PubMed] [Google Scholar]
41.Olatunji BO, Cisler JM, Tolin DF. Quality of life in the anxiety disorders: a meta-analytic review. Clin Psychol Rev. 2007;27(5):572–581. doi: 10.1016/j.cpr.2007.01.015. [DOI] [PubMed] [Google Scholar]
42.Maj M. Helpful treatment of depression-delivering the right messages. JAMA Psychiatry. 2020;77(8):784–786. doi: 10.1001/jamapsychiatry.2020.0363. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

12888_2021_3363_MOESM1_ESM.docx^{(93.5KB, docx)}

Data Availability Statement

[CR1] 1.Ruscio AM, Hallion LS, Lim CCW, Aguilar-Gaxiola S, Al-Hamzawi A, Alonso J, et al. Cross-sectional comparison of the epidemiology of DSM-5 generalized anxiety disorder across the globe. JAMA Psychiatry. 2017;74(5):465–475. doi: 10.1001/jamapsychiatry.2017.0056. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR2] 2.Alonso J, Petukhova M, Vilagut G, Chatterji S, Heeringa S, Üstün TB, et al. Days out of role due to common physical and mental conditions: results from the WHO world mental health surveys. Mol Psychiatry. 2011;16(12):1234–46. 10.1038/mp.2010.101. [DOI] [PMC free article] [PubMed]

[CR3] 3.Hoffman DL, Dukes EM, Wittchen HU. Human and economic burden of generalized anxiety disorder. Depress Anxiety. 2008;25(1):72–90. doi: 10.1002/da.20257. [DOI] [PubMed] [Google Scholar]

[CR4] 4.Carl E, Witcraft SM, Kauffman BY, Gillespie EM, Becker ES, Cuijpers P, et al. Psychological and pharmacological treatments for generalized anxiety disorder (GAD): a meta-analysis of randomized controlled trials. Cogn Behav Ther. 2020;49(1):1–21. 10.1080/16506073.2018.1560358. [DOI] [PMC free article] [PubMed]

[CR5] 5.Mitte K. Meta-analysis of cognitive-behavioral treatments for generalized anxiety disorder: a comparison with pharmacotherapy. Psychol Bull. 2005;131(5):785–795. doi: 10.1037/0033-2909.131.5.785. [DOI] [PubMed] [Google Scholar]

[CR6] 6.Robichaud M, Koerner N, Dugas MJ. Cognitive behavioral treatment for generalized anxiety disorder: from science to practice: Routledge; 2019. 10.4324/9781315709741.

[CR7] 7.Stein DJ. Evidence-based treatment of anxiety disorders. Int J Psychiatry Clin Pract. 2006;10(sup1):16–21. [DOI] [PubMed]

[CR8] 8.Hoertel N, Le Strat Y, Blanco C, Lavaud P, Dubertret C. Generalizability of clinical trial results for generalized anxiety disorder to community samples. Depress Anxiety. 2012;29(7):614–620. doi: 10.1002/da.21937. [DOI] [PubMed] [Google Scholar]

[CR9] 9.Heneghan C, Goldacre B, Mahtani KR. Why clinical trial outcomes fail to translate into benefits for patients. Trials. 2017;18(1):122. doi: 10.1186/s13063-017-1870-2. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR10] 10.Janiaud P, Dal-Ré R, Ioannidis JPA. Assessment of pragmatism in recently published randomized clinical trials. JAMA Intern Med. 2018;178(9):1278–1280. doi: 10.1001/jamainternmed.2018.3321. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR11] 11.Sheehan DV, Harnett-Sheehan K, Spann ME, Thompson HF, Prakash A. Assessing remission in major depressive disorder and generalized anxiety disorder clinical trials with the discan metric of the Sheehan disability scale. Int Clin Psychopharmacol. 2011;26(2):75–83. doi: 10.1097/YIC.0b013e328341bb5f. [DOI] [PubMed] [Google Scholar]

[CR12] 12.Kazdin AE. Research design in clinical psychology (5th ed.) Boston, MA: Pearson; 2017. [Google Scholar]

[CR13] 13.Cocklin AA, Mansell W, Emsley R, McEvoy P, Preston C, Comiskey J, et al. Client perceptions of helpfulness in therapy: a novel video-rating methodology for examining process variables at brief intervals during a single session. Behav Cogn Psychother. 2017;45(6):647–60. 10.1017/S1352465817000273. [DOI] [PubMed]

[CR14] 14.Colman E, Missinne S, Bracke P. The role of perceived helpfulness in predicting subjective unmet need and the frequency of health care use. Arch Psychiatr Nurs. 2014;28(1):43–49. doi: 10.1016/j.apnu.2013.10.007. [DOI] [PubMed] [Google Scholar]

[CR15] 15.Lee SH, Ahn SC, Lee YJ, Choi TK, Yook KH, Suh SY. Effectiveness of a meditation-based stress management program as an adjunct to pharmacotherapy in patients with anxiety disorder. J Psychosom Res. 2007;62(2):189–195. doi: 10.1016/j.jpsychores.2006.09.009. [DOI] [PubMed] [Google Scholar]

[CR16] 16.Mojtabai R, Olfson M, Sampson NA, Jin R, Druss B, Wang PS, et al. Barriers to mental health treatment: results from the National Comorbidity Survey Replication (NCS-R). Psychol Med. 2011;41(8):1751–61. 10.1017/S0033291710002291. [DOI] [PMC free article] [PubMed]

[CR17] 17.Alang SM, McAlpine DD. Pathways to mental health services and perceptions about the effectiveness of treatment. Soc Ment Health. 2019;9(3):388–407. doi: 10.1177/2156869318802341. [DOI] [Google Scholar]

[CR18] 18.Cuijpers P. Targets and outcomes of psychotherapies for mental disorders: an overview. World Psychiatry. 2019;18(3):276–285. doi: 10.1002/wps.20661. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR19] 19.Sharma T, Bamford M, Dodman D. Person-centred care: an overview of reviews. Contemp Nurse. 2015;51(2–3):107–120. doi: 10.1080/10376178.2016.1150192. [DOI] [PubMed] [Google Scholar]

[CR20] 20.Harris MG, Kazdin AE, Chiu WT, Sampson NA, Aguilar-Gaxiola S, Al-Hamzawi A, et al. Findings from world mental health surveys of the perceived helpfulness of treatment for patients with major depressive disorder. JAMA Psychiatry. 2020;77(8):830–841. doi: 10.1001/jamapsychiatry.2020.1107. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR21] 21.Stein DJ, Harris MG, Vigo DV, Tat Chiu W, Sampson N, Alonso J, et al. Perceived helpfulness of treatment for posttraumatic stress disorder: findings from the world mental health surveys. Depress Anxiety. 2020;37(10):972–94. 10.1002/da.23076. [DOI] [PMC free article] [PubMed]

[CR22] 22.Kessler RC, Ustun TB. The WHO mental health surveys. Global perspectives on the epidemiology of mental disorders. Cambridge, England: Cambridge University Press; 2008. [Google Scholar]

[CR23] 23.Kessler RC, Ustün TB. The world mental health (WMH) survey initiative version of the World Health Organization (WHO) composite international diagnostic interview (CIDI) Int J Methods Psychiatr Res. 2004;13(2):93–121. doi: 10.1002/mpr.168. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR24] 24.Harkness J, Pennell B, Villar A, Gebler N, Aguilar-Gaxiola S, Bilgen I. Translation procedures and translation assessment in the world mental health survey initiative. In: Kessler R, Üstün T, editors. The WHO world mental health surveys: global perspectives on the epidemiology of mental disorders. New York, NY: Cambridge University Press; 2008. pp. 91–113. [Google Scholar]

[CR25] 25.Heeringa S, Wells J, Hubbard F, Mneimneh Z, Chiu W, Sampson N, et al. Sample designs and sampling procedures. In: Kessler R, Üstün T, et al., editors. The WHO world mental health surveys: global perspectives on the epidemiology of mental disorders. New York, NY: Cambridge University Press; 2008. pp. 14–32. [Google Scholar]

[CR26] 26.Ruscio AM, Lane M, Roy-Byrne P, Stang PE, Stein DJ, Wittchen H-U, et al. Should excessive worry be required for a diagnosis of generalized anxiety disorder? Results from the US National Comorbidity Survey Replication. Psychol Med. 2005;35(12):1761–1772. doi: 10.1017/S0033291705005908. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR27] 27.Spitzer M, Robert L, Gibbon M, Williams J. Structured clinical interview for DSM-IV-TR axis I disorders, research version, non-patient edition (SCID-I/NP) New York: Biometrics Research, New York State Psychiatric Institute; 2002. [Google Scholar]

[CR28] 28.Haro JM, Arbabzadeh-Bouchez S, Brugha TS, De Girolamo G, Guyer ME, Jin R, et al. Concordance of the composite international diagnostic interview version 3.0 (CIDI 3.0) with standardized clinical assessments in the WHO world mental health surveys. Int J Methods Psychiatr Res. 2006;15(4):167–180. doi: 10.1002/mpr.196. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR29] 29.Ruscio AM, Chiu WT, Roy-Byrne P, Stang PE, Stein DJ, Wittchen HU, et al. Broadening the definition of generalized anxiety disorder: effects on prevalence and associations with other disorders in the National Comorbidity Survey Replication. J Anxiety Disord. 2007;21(5):662–76. 10.1016/j.janxdis.2006.10.004. [DOI] [PMC free article] [PubMed]

[CR30] 30.American Psychiatric Association . Diagnostic and statistical manual of mental disorders (5th ed) Washington, DC: American Psychiatric Press; 2013. [Google Scholar]

[CR31] 31.Knäuper B, Cannell CF, Schwarz N, Bruce ML, Kessler RC. Improving accuracy of major depression age-of-onset reports in the US National Comorbidity Survey. Int J Methods Psychiatr Res. 1999;8(1):39–48. doi: 10.1002/mpr.55. [DOI] [Google Scholar]

[CR32] 32.Merikangas KR, Jin R, He JP, Kessler RC, Lee S, Sampson NA, et al. Prevalence and correlates of bipolar spectrum disorder in the world mental health survey initiative. Arch Gen Psychiatry. 2011;68(3):241–51. 10.1001/archgenpsychiatry.2011.12. [DOI] [PMC free article] [PubMed]

[CR33] 33.Halli SS, Rao KV. Advanced techniques of population analysis. Springer Science & Business Media: Boston, MA; 2013. [Google Scholar]

[CR34] 34.Willett JB, Singer JD. Investigating onset, cessation, relapse, and recovery: why you should, and how you can, use discrete-time survival analysis to examine event occurrence. J Conult Clin Psychol. 1993;61(6):952–965. doi: 10.1037/0022-006X.61.6.952. [DOI] [PubMed] [Google Scholar]

[CR35] 35.Wolter K. Introduction to variance estimation. Springer- Verlag: New York, NY; 1985. [Google Scholar]

[CR36] 36.SAS/ STAT . 14.3 software version 9.4 [computer program] Cary, NC: SAS Institute Inc; 2016. [Google Scholar]

[CR37] 37.de Vries YA, Harris MG, Vigo D, Chiu WT, Sampson NA, Al-Hamzawi A, et al. Perceived helpfulness of treatment for specific phobia: findings from the world mental health surveys. J Affect Disord. 2021;288:199–209. doi: 10.1016/j.jad.2021.04.001. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR38] 38.Bruce SE, Yonkers KA, Otto MW, Eisen JL, Weisberg RB, Pagano M, et al. Influence of psychiatric comorbidity on recovery and recurrence in generalized anxiety disorder, social phobia, and panic disorder: a 12-year prospective study. Am J Psychiatry. 2005;162(6):1179–87. 10.1176/appi.ajp.162.6.1179. [DOI] [PMC free article] [PubMed]

[CR39] 39.Kessler RC, McLaughlin KA, Green JG, Gruber MJ, Sampson NA, Zaslavsky AM, et al. Childhood adversities and adult psychopathology in the WHO world mental health surveys. Br J Psychiatry. 2010;197(5):378–385. doi: 10.1192/bjp.bp.110.080499. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR40] 40.Zlomuzica A, Dere D, Machulska A, Adolph D, Dere E, Margraf J. Episodic memories in anxiety disorders: clinical implications. Front Behav Neurosci. 2014;8:131. doi: 10.3389/fnbeh.2014.00131. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR41] 41.Olatunji BO, Cisler JM, Tolin DF. Quality of life in the anxiety disorders: a meta-analytic review. Clin Psychol Rev. 2007;27(5):572–581. doi: 10.1016/j.cpr.2007.01.015. [DOI] [PubMed] [Google Scholar]

[CR42] 42.Maj M. Helpful treatment of depression-delivering the right messages. JAMA Psychiatry. 2020;77(8):784–786. doi: 10.1001/jamapsychiatry.2020.0363. [DOI] [PubMed] [Google Scholar]

PERMALINK

Perceived helpfulness of treatment for generalized anxiety disorder: a World Mental Health Surveys report

Dan J Stein

Alan E Kazdin

Ayelet Meron Ruscio

Wai Tat Chiu

Nancy A Sampson

Hannah N Ziobrowski

Sergio Aguilar-Gaxiola

Ali Al-Hamzawi

Jordi Alonso

Yasmin Altwaijri

Ronny Bruffaerts

Brendan Bunting

Giovanni de Girolamo

Peter de Jonge

Louisa Degenhardt

Oye Gureje

Josep Maria Haro

Meredith G Harris

Aimee Karam

Elie G Karam

Viviane Kovess-Masfety

Sing Lee

Maria Elena Medina-Mora

Jacek Moskalewicz

Fernando Navarro-Mateu

Daisuke Nishi

José Posada-Villa

Kate M Scott

Maria Carmen Viana

Daniel V Vigo

Miguel Xavier

Zahari Zarkov

Ronald C Kessler

Abstract

Background

Methods

Results

Conclusions

Supplementary Information

Background

Methods

Samples

Measures

Generalized anxiety disorder (GAD)

Perceived helpfulness of treatment for GAD

Predictors of obtaining helpful treatment for GAD

Analysis methods

Results

GAD prevalence, treatment, and perceived helpfulness of treatment

Table 1.

Helpful GAD treatment across professionals seen

Table 2.

Persistence with help-seeking for GAD following treatment failure

Table 3.

Predictors of obtaining helpful treatment for GAD

Table 4.

Discussion

Supplementary Information

Acknowledgements

Abbreviations

Authors’ contributions

Funding

Availability of data and materials

Declarations

Ethics approval and consent to participate

Consent for publication

Competing interests

Footnotes

Contributor Information

References

Associated Data

Supplementary Materials

Data Availability Statement

ACTIONS

PERMALINK

RESOURCES

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