Skip to main content
PLOS One logoLink to PLOS One
. 2024 Mar 13;19(3):e0296949. doi: 10.1371/journal.pone.0296949

Response to anxiety treatment before, during, and after the COVID-19 pandemic

David H Rosmarin 1,2,*, Steven Pirutinsky 2,3
Editor: Mohammad Farris Iman Leong Bin Abdullah4
PMCID: PMC10936764  PMID: 38478468

Abstract

Background

The COVID-19 pandemic yielded a substantial increase in worldwide prevalence and severity of anxiety, but less is known about effects on anxiety treatment.

Objective

We evaluated effects of the COVID-19 pandemic on responses to Cognitive Behavioral Therapy for anxiety, in a clinically heterogeneous sample of patients.

Methods

A sample of 764 outpatients were separated into four groups: (1) Pre-pandemic (start date on or prior to 12/31/2019), (2) Pandemic-Onset (start date from 01/01/2020 to 03/31/2020), (3) During-Pandemic (start date from 04/01/2020 through 12/31/2020), and (4) Post-Pandemic (start date on or after 01/01/2021). We subsequently compared treatment trajectories and effects within and between these groups over 5621 total time points (mean of 7.38 measurements per patient).

Results

Overall, patients presented with moderate levels of anxiety (M = 13.25, 95%CI: 12.87, 13.62), which rapidly decreased for 25 days (M = 9.46, 95%CI: 9.09, 9.83), and thereafter slowly declined into the mild symptom range over the remainder of the study period (M = 7.36, 95%CI: 6.81, 7.91), representing clinically as well as statistically significant change. A series of conditional multilevel regression models indicated that there were no substantive differences between groups, and no increase in anxiety during the acute pandemic phase.

Conclusions

Our results suggest that responses to treatment for anxiety were equivalent before, during, and after the COVID-19 pandemic. Among patients who were in treatment prior to the pandemic, we failed to detect an increase in anxiety during the pandemic’s acute phase (March 20th, 2020 through July 1st, 2020).

Introduction

It is well established that the COVID-19 pandemic led to adverse effects on mental health for the population as a whole [15], and vulnerable subgroups in particular [6, 7]. Anxiety demonstrably increased substantially from the pandemic’s onset in early 2020 [810], through the first availability of vaccinations in early 2021 (dubbed by some as the “light at the end of the tunnel”) [11]. To quantify these trends: One large meta-analytic study with over two million adults found that 35% had significant anxiety during the pandemic [2], and the World Health Organization estimated a 25% increase overall [12, 13]. These effects are not surprising given that intolerance of uncertainty–which was rampant during the pandemic given high levels of perceived threat–is a key factor in the development and severity of anxiety [14, 15].

Less is known about the effects of the pandemic on treatment for anxiety. On the one hand, there is reason to believe that COVID-19 was detrimental to anxiety treatment. During 2020, several helpful commentaries and case reports were rapidly published to provide clinicians with specific strategies to support patients with pre-existing anxiety by bolstering treatment delivery [16, 17]. In retrospect, these efforts were well-warranted since it is now known that a history of mental health treatment prior to the pandemic predicted greater likelihood of having symptoms meeting criteria for Generalized Anxiety Disorder during the pandemic [18]. On the other hand, one study found that individuals who received Cognitive Behavioral Therapy (CBT) for social anxiety disorder prior to the pandemic, benefited from enduring effects [19]. Similarly, in another study of patients with severe obsessive-compulsive disorder, the trajectory and outcomes of intensive CBT was similar among those receiving treatment prior to vs. during the pandemic [20]. These findings are encouraging, and may suggest that the acquisition of cognitive and behavioral skills is a harbinger of better mental health, even in the context of uniquely high worldwide stress. However, further research in more clinically diverse samples is needed to assess whether CBT for anxiety was equally effective for those who entered treatment during the pandemic, compared to before, or after.

We therefore evaluated responses to anxiety treatment before, during, and after the pandemic, in a clinically heterogeneous sample of patients presenting to a naturalistic outpatient setting. We separated patients into four groups, in accordance with a COVID-19 pandemic timeline proposed by the Yale School of Medicine [21]: (1) Pre-pandemic: Those who entered and completed treatment before the start of the pandemic (start date on or prior to 12/31/2019); (2) Pandemic-Onset: Those who were in treatment during the onset of the pandemic (start date from 01/01/2020 to 03/31/2020); (3) During-Pandemic: Those who commenced treatment after the onset of the pandemic (start date from 04/01/2020 through 12/31/2020); and (4) Post-Pandemic: Those who entered treatment once vaccines started to become available (start date after 01/01/2021). Subsequently, we assessed and compared treatment trajectories and effects within and between these groups. We also examined whether patients in treatment during the pandemic experienced any specific changes in anxiety during the initial acute phase of COVID-19 (March 20th 2020 through July 1st 2020). We hypothesized that patients presenting to treatment prior to (group 1) and after the pandemic (group 4) would benefit more from treatment than those who received treatment during the pandemic’s onset or prior to the availability of vaccines (groups 2 and 3). We further hypothesized that anxiety would worsen during the initial acute phase of the pandemic.

Materials and methods

Procedures & participants

Data was collected from adult patients presenting to the offices of Center for Anxiety, a multisite outpatient clinic in the northeastern United States between 10/1/2019 and 3/1/2021. The study was approved by the Touro University Institutional Review Board for the Protection of Human Subjects, protocol # IRB1-2023-003. At treatment intake, patients provided written informed consent to have data from their clinical questionnaires and medical records used in research. Medical record data was assessed retrospectively and was fully de-identified prior to access by the study team. At intake and at each treatment session, patients were asked to complete self-report measures of anxiety using Psych-Surveys™ software. At intake, patients also received a general psychosocial interview, as well as the Miniature International Neuropsychiatric Interview [22]. Inclusion criteria for the current study included age 18 years or older, and completion of anxiety measure at intake plus at least three additional times within the first 100 days treatment. We included only measurements that took place within the first 100 days of treatment, since measurements post 100 days were highly variable and sparse; this resulted in the exclusion of only 0.3% of patients. Our final sample included 764 patients, with anxiety assessed at 5621 total time points, representing a mean average 7.38 anxiety measurements per patient. Group sizes were as follows: Pre-pandemic (n = 221), (2) Pandemic-Onset (n = 42), (3) During-Pandemic (n = 104), (4) Post-Pandemic (n = 384).

All patients were provided with Cognitive-Behavioral Therapy (CBT) and/or Dialectical Behavior Therapy (DBT) as per usual clinic procedures. While no standardized treatment protocols were used given the naturalistic setting, a chart review revealed that a variety of specific cognitive and dialectical behavior therapy techniques were utilized including psychoeducation, monitoring of symptoms/target behaviors (e.g., thought records, diary cards), exposure, response prevention, behavioral activation, identifying and restructuring cognitive distortions, as well as mindfulness and acceptance. Therapists included doctoral level trainees as well as master’s level clinicians, all of whom received weekly supervision and additional consultation as needed throughout treatment by a licensed provider. This study was approved by the Touro University Institutional Review Board for the Protection of Human Subjects.

Measures

Demographic information was collected from electronic health records, and obtained from patients using a combination of self-report items and a semi-structured interview at intake.

Diagnoses were assessed with Miniature International Neuropsychiatric Interview [22], and conferred by supervising licensed doctoral-level staff.

Levels of anxiety were assessed at intake and each subsequent session using the GAD-7, a seven-item self-report measure of generalized anxiety symptoms that is used to assess for anxiety in a variety of clinical settings [23]. The scale yields a single total score between 0 and 21 and can be interpreted using four validated levels of anxiety severity: “Minimal” (0–4) “Mild” (5–9); “Moderate” (10–14) and “Severe” (15–21) [23].

Statistical analyses

Given unequal group sizes, we modeled changes in anxiety over the course of treatment using multilevel growth curve models [24], which are widely used in psychotherapy research since they are robust, allow for missing data, handle designs with varying measurement times, and control for unmeasured between-subject differences. Models were estimated with the lme4 library [25] using restricted maximum likelihood estimation, and coefficients tested with the lmerTest library [26] in the R programming language [27]. Non-linear terms were constructed using Orthogonal Polynomials estimated by the poly function in the stats package [27], plots were created using the sjPlot library [28]. Descriptive statistics and preliminary analyses were calculated in SPSS 23.

Power analyses for longitudinal multilevel regression models require complex simulations with extensive assumptions to provide accurate estimates of power [29]. Given the complex nature of our analyses, we were unable to develop reasonable assumptions. However, previous simulation studies indicate that multilevel modeling is highly robust and yields unbiased estimates of fixed effects even in small samples (e.g., as many as 10 groups with as few as five units each [30], and that these models generally require few cases to have sufficient power (e.g., as many as 50 groups with as few as five observations each [31]). Following these heuristics, we estimated that the current sample was likely to capture even small effects.

Results

Preliminary analyses

Demographic and clinical characteristics of each group within the sample are presented in Table 1. Results indicated that groups did not differ significantly in terms of any demographic variables. Subsequent analyses therefore did not include demographic covariates. Similarly, or diagnoses and levels of anxiety at intake were also statistically equivalent between groups. Groups also had equivalent numbers of weekly sessions, suggesting that treatment was not more or less intensive for any particular group.

Table 1. Demographic & clinical characteristics of the sample.

Variable Pre-pandemic (on or before 12/31/2019) Pandemic-Onset (01/01/2020-03/31/2020 During-Pandemic (04/01/2020-12/31/2020) Post-Pandemic (1/1/2021 and thereafter) Test Statistics
n 221 42 104 384
Demographic Characteristics
Age M(SD) 30.67 (10.68) (26.42) 7.87 35.34 (15.47) 31.92 (13.77) F(3,550) = 3.79
Gender (female) 63% 71% 56% 61% χ2(6,598) = 15.90
Marital Status Single 64% Single 76% Single 58% Single 67% X2(15,600) = 13.01
Married 28% Married 24% Married 29% Married 25%
Sep/Div 5% Sep/Div 0% Sep/Div 7% Sep/Div 4%
Cohab 3% Cohab 0% Cohab 6% Cohab 3%
Household size M(SD) 3.11 (1.55) 2.88 (1.61) 2.93 (1.58) 2.95 (1.54) F(3,596) = .62
College Graduate 63% 67% 63% 64% χ2 (12,600) = 14.12
Unemployed 11% 7% 13% 11% χ2(21,600) = 26.29
Clinical Characteristic
Anxiety M = 13.52 M = 14.38 M = 13.33 M = 13.10 F(3, 598) = .75
M (SD) SD = 5.18 SD = 5.20 SD = 5.79 SD = 5.35
Diagnoses Anxiety 66% Anxiety 50% Anxiety 62% Anxiety 64% χ2 (3, 554) < 8.4
OC 23% OC 8% OC 20% OC 23% for all analyses
Mood 39% Mood 50% Mood 45% Mood 41%
Other 12% Other 16% Other 18% Other 30%
Weekly Sessions .86 (.52) .92 (.39) .92 (.53) .84 (.44) F(3, 748) = 1.11

Notes: All tests were not significant (p-level adjusted for multiple comparisons); n differs slightly between analyses due to missing data for some patients; Unemployed excludes homemakers, students, and retirees; Anxiety refers to GAD-7 scores at intake; Diagnoses sum to more than 100% as some patients presented with multiple concerns.

Treatment effects

Examination of raw treatment trajectories (Fig 1) suggested that changes in anxiety over the course of treatment was best described by a cubic pattern, with an initial period of rapid decline lasting roughly 25 days followed by a longer period of slower improvement that slowly trailed off over roughly 75 days. Consistent with these descriptive data and previous research [32] results indicated that a model allowing for individual random variation in the linear and non-linear rates of change was the best fit for our data (Table 2). Specifically, cubic models fit significantly better than simpler linear models (∆AIC = -10.99, ∆BIC = -5.36, χ2(1) = 12.99, p = .0003), quadratic models (∆AIC = -10.99, ∆BIC = -5.36, χ2(1) = 12.99, p = .0003) and log-linear models (∆AIC = -10.99, ∆BIC = -5.36, χ2(1) = 12.99, p = .0003). Coefficients for a baseline cubic treatment model are presented in Table 3. These indicate that on average, patients presented with moderate levels of anxiety (M = 13.25, 95%CI: 12.87, 13.62), which rapidly decreased for 25 days (M = 9.46, 95%CI: 9.09, 9.83), and thereafter slowly declined into the mild symptom range over the remainder of the study period (M = 7.36, 95%CI: 6.81, 7.91). These results represent both clinically as well as statistically significant change in the sample as a whole.

Fig 1. Changes in anxiety before, during, and after the COVID-19 pandemic.

Fig 1

Table 2. Multilevel regression models of anxiety over the course of clinical treatment.

df AIC BIC -2LL Χ 2 p
Baseline Models
    M0: Intercept Only 3 319009 31929 -15951
    M1: Linear Time 6 30424 30463 -15206 1491.27 < .0001
    M2: Quadric Time 10 29739 29806 -14860 692.31 < .0001
    M3: Cubic Time 15 29508 29608 -14739 241.17 < .0001
Conditional Models
    M4: Intake period (Intercept only) 18 29511 29630 -14737 3.46 0.33
    M5: Intake period (Slopes) 27 29521 29700 -14733 7.80 0.55
    M6: Acute Pandemic (Intercept) 28 29522 29708 -14733 .62 0.43

Notes: All models were based on 764 patients and 5621 observations and including random intercepts and slopes for each patient

Table 3. Unconditional multilevel regression models (treatment effects).

Fixed Effects B SE t p
Intercept 9.65 0.17 57.76 < .00001
Linear Time -118.85 5.30 22.42 < .00001
Quadratic Time 61.36 4.28 14.32 < .00001
Cubic Time -26.60 3.62 7.34 < .00001
Random Effects SD Linear Quadratic Cubic
Intercept 4.43 .03 -.26 .08
Linear Time 107.50 -.21 -.30
Quadratic Time 84.83 -.54
Cubic Time 2.31

Notes: Model based on n = 764 patients and 5621 observations; Time represents the number of days since intake and was coded using Orthogonal Polynomials.

Pandemic effects

Building upon the above baseline model, we estimated a series of conditional multilevel regression models to assess if the course of anxiety differed between the above-mentioned four groups in our sample: (1) Pre-pandemic, (2) Pandemic-Onset, (3) During-Pandemic, (4) Post-Pandemic. Model comparisons are reported in Table 3 and indicate that there were no substantive differences between these groups: All entered treatment with roughly the same (moderate) levels of anxiety, all progressed through treatment in a similar cubic pattern, and all terminated with similar (mild) levels of anxiety. These results suggest that responses to psychotherapy for anxiety were equivalent before, during, and after the COVID-19 pandemic. Furthermore, among patients who were in treatment at the start of the pandemic (groups 2 and 3), an additional model assessing whether levels of anxiety increased during the initial acute phase of COVID-19 (March 20th 2020 through July 1st 2020) was similarly non-significant, suggesting that existing patients did not experience increased in anxiety over that time (Table 2, Model M6).

Discussion

In this study, we examined effects and trajectories of anxiety treatment within a large and clinically diverse sample of patients presenting prior to, during, and after the COVID-19 pandemic. Contrary to our expectations, the course of anxiety and its treatment effects were equivalent among patients, irrespective of when they entered treatment. That is, irrespective of when patients commenced or terminated treatment, they had roughly the same levels of anxiety at the start of treatment, they then experienced a cubic pattern of anxiety change characterized by an initial period of rapid decline lasting roughly 25 days, followed by a longer period of slower improvement that slowly trailed off over roughly 75 days, and treatment resulted in similar levels of anxiety 100 days after patients’ initial sessions. These results are consistent with a large body of literature highlighting the efficacy and effectiveness of CBT for anxiety-related concerns (e.g., [3335]), which includes several studies demonstrating large, stable, and enduring effects [3638]. Our findings support and extend this work by suggesting that treatments for anxiety are effective, even in the context of uniquely heightened periods of prolonged stress. While treatment was not standardized, the naturalistic setting of our study has ecological validity and highlights the real-world value of CBT and DBT, even when delivered under unusual conditions.

Of potentially even greater significance, we found that pre-pandemic patients did not experience a discernable increase in anxiety during the initial acute phase of COVID-19. As noted above, this period of time was marked by significant mental distress [810] due to intense uncertainty, strain, and social isolation. The initiation of the COVID-19 pandemic was likely of particular concern for anxiety treatment-seekers, who experienced the additional stress of shifting to 100% telehealth in delivering their treatment, over the span of just a few weeks. Our findings optimistically suggests that the acquisition of psychosocial skills is a key predictor of mental health, wellbeing, and resilience–those who acquire such skills can benefit, even when facing to significant life stressors. Our findings also suggests that, ironically, those who experienced anxiety prior to the pandemic and took the opportunity to enter treatment, may have been better off than others who had never experienced significant anxiety before the pandemic. In this regard, previous experience of anxiety leading to treatment may reduce future susceptibility to symptoms in the context of increased stress.

Our study has several limitations that should be noted. First, our sample was demographically and clinically diverse, but highly educated overall and geographically specific to the northeastern United States. Treatment effects over the course of the pandemic might have been different within other regions, countries, or populations. Second, while multilevel modeling is robust to differences in group size, the pandemic-onset group was substantially smaller than the others. While this likely represents a smaller date range for group 3, it may also reflect that timing of psychosocial challenges and limited availability of in-person services can preclude entry into treatment. Our results should therefore not be construed to represent or reflect aggregate effects of stressors on anxiety overall, rather effects of the pandemic on the course and effects of symptoms among treatment-seekers. Finally, our study is limited to an analysis of anxiety, and treatment effects on other symptoms such as depression and substance abuse–both of which increased substantially during the pandemic [39, 40]–might have varied over the course of 2020.

In sum, our results indicate that response to anxiety treatment was strikingly similar for patients presenting before, during, and after the COVID-19 pandemic, suggesting that acquisition of skills to cope with anxiety is protective even in the context of a global crisis.

Data Availability

Data are publicly available from OSF at https://osf.io/yusdk/.

Funding Statement

The authors received no specific funding for this work.

References

  • 1.Amsalem D, Dixon LB, Neria Y. The Coronavirus Disease 2019 (COVID-19) Outbreak and Mental Health: Current Risks and Recommended Actions. JAMA Psychiatry. 2021;78(1):9–10. doi: 10.1001/jamapsychiatry.2020.1730 [DOI] [PubMed] [Google Scholar]
  • 2.Delpino FM, da Silva CN, Jerônimo JS, Mulling ES, da Cunha LL, Weymar MK, et al. Prevalence of anxiety during the COVID-19 pandemic: A systematic review and meta-analysis of over 2 million people. J Affect Disord. 2022;318:272–282. doi: 10.1016/j.jad.2022.09.003 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Xiong J, Lipsitz O, Nasri F, Lui LMW, Gill H, Phan L, et al. Impact of COVID-19 pandemic on mental health in the general population: A systematic review. J Affect Disord. 2020;277:55–64. doi: 10.1016/j.jad.2020.08.001 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Kumar A, Nayar KR. COVID 19 and its mental health consequences. J Ment Health. 2021;30(1):1–2. doi: 10.1080/09638237.2020.1757052 [DOI] [PubMed] [Google Scholar]
  • 5.Office of the Surgeon General (OSG). Protecting Youth Mental Health: The U.S. Surgeon General’s Advisory. Washington (DC): US Department of Health and Human Services; 2021. [PubMed] [Google Scholar]
  • 6.Thomeer MB, Moody MD, Yahirun J. Racial and Ethnic Disparities in Mental Health and Mental Health Care During The COVID-19 Pandemic. J Racial and Ethnic Health Disparities. 2023;10(2):961–976. doi: 10.1007/s40615-022-01284-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Muller AE, Hafstad EV, Himmels JPW, Smedslund G, Flottorp S, Stensland SØ, et al. The mental health impact of the covid-19 pandemic on healthcare workers, and interventions to help them: A rapid systematic review. Psychiatry Res. 2020;293:113441. doi: 10.1016/j.psychres.2020.113441 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Hyland P, Shevlin M, McBride O, Murphy J, Karatzias T, Bentall RP, et al. Anxiety and depression in the Republic of Ireland during the COVID‐19 pandemic. Acta Psychiatr Scand. 2020;142(3):249–256. doi: 10.1111/acps.13219 [DOI] [PubMed] [Google Scholar]
  • 9.Pashazadeh Kan F, Raoofi S, Rafiei S, Khani S, Hosseinifard H, Tajik F, et al. A systematic review of the prevalence of anxiety among the general population during the COVID-19 pandemic. J Affect Disord. 2021;293:391–398. doi: 10.1016/j.jad.2021.06.073 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Mann FD, Krueger RF, Vohs KD. Personal economic anxiety in response to COVID-19. Pers Individ Dif. 2020;167:110233. doi: 10.1016/j.paid.2020.110233 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Chu H, Liu S. Light at the end of the tunnel: Influence of vaccine availability and vaccination intention on people’s consideration of the COVID-19 vaccine. Soc Sci Med. 2021;286:114315. doi: 10.1016/j.socscimed.2021.114315 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.World Health Organization [Internet]. COVID-19 pandemic triggers 25% increase in prevalence of anxiety and depression worldwide. [cited June 16, 2023]. Available from: https://www.who.int/news/item/02-03-2022-covid-19-pandemic-triggers-25-increase-in-prevalence-of-anxiety-and-depression-worldwide [Google Scholar]
  • 13.Santomauro DF, Mantilla Herrera AM, Shadid J, Zheng P, Ashbaugh C, Pigott D, et al. Global prevalence and burden of depressive and anxiety disorders in 204 countries and territories in 2020 due to the COVID-19 pandemic. The Lancet. 2021;398(10312):1700–1712. doi: 10.1016/S0140-6736(21)02143-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Chen S, Yao N, Qian M. The influence of uncertainty and intolerance of uncertainty on anxiety. J Behav Ther Exp Psychiatry. 2018;61:60–65. doi: 10.1016/j.jbtep.2018.06.005 [DOI] [PubMed] [Google Scholar]
  • 15.Carleton RN, Mulvogue MK, Thibodeau MA, McCabe RE, Antony MM, Asmundson GJG. Increasingly certain about uncertainty: Intolerance of uncertainty across anxiety and depression. J Anxiety Disord. 2012;26(3):468–479. doi: 10.1016/j.janxdis.2012.01.011 [DOI] [PubMed] [Google Scholar]
  • 16.Shafran R, Rachman S, Whittal M, Radomsky A, Coughtrey A. Fear and Anxiety in COVID-19: Preexisting Anxiety Disorders. Cogn Behav Pract. 2021;28(4):459–467. doi: 10.1016/j.cbpra.2021.03.003 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Satre DD, Iturralde E, Ghadiali M, Young-Wolff KC, Campbell CI, Leibowitz AS, et al. Treatment for Anxiety and Substance Use Disorders During the COVID-19 Pandemic: Challenges and Strategies. J Addict Med. 2020;14(6):e293–e296. doi: 10.1097/ADM.0000000000000755 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Turna J, Zhang J, Lamberti N, Patterson B, Simpson W, Francisco AP, et al. Anxiety, depression and stress during the COVID-19 pandemic: Results from a cross-sectional survey. J Psychiatr Res. 2021;137:96–103. doi: 10.1016/j.jpsychires.2021.02.059 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Samantaray N, Kar N, Mishra SR. A follow-up study on treatment effects of cognitive-behavioral therapy on social anxiety disorder: Impact of COVID-19 fear during post-lockdown period. Psychiatry Res. 2022;310:114439. doi: 10.1016/j.psychres.2022.114439 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Pinciotti CM, Bulkes NZ, Horvath G, Riemann BC. Efficacy of intensive CBT telehealth for obsessive-compulsive disorder during the COVID-19 pandemic. J Obsessive Compuls Relat Disord. 2022;32:100705. doi: 10.1016/j.jocrd.2021.100705 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Patella K. Our Pandemic Year—A COVID-19 Timeline. Yale Medicine [Internet]. 2021. Mar 9. [cited June 16, 2023]. Available from: https://www.yalemedicine.org/news/covid-timeline [Google Scholar]
  • 22.Sheehan DV, Sheehan KH, Shytle RD, Janavs J, Bannon Y, Rogers JE, et al. Reliability and Validity of the Mini International Neuropsychiatric Interview for Children and Adolescents (MINI-KID). J Clin Psychiatry. 2010;71(03):313–326. doi: 10.4088/JCP.09m05305whi [DOI] [PubMed] [Google Scholar]
  • 23.Spitzer RL, Kroenke K, Williams JBW, Löwe B. A Brief Measure for Assessing Generalized Anxiety Disorder: The GAD-7. Arch Intern Med. 2006;166(10):1092. doi: 10.1001/archinte.166.10.1092 [DOI] [PubMed] [Google Scholar]
  • 24.Singer JD, Willett JB. Applied Longitudinal Data Analysis: Modeling Change and Event Occurrence. 1st ed. New York, NY: Oxford University Press; 2003. doi: 10.1093/acprof:oso/9780195152968.001.0001 [DOI] [Google Scholar]
  • 25.Bates D, Mächler M, Bolker B, Walker S. Fitting Linear Mixed-Effects Models Using lme4. J Stat Soft. 2015;67(1). doi: 10.18637/jss.v067.i01 [DOI] [Google Scholar]
  • 26.Kuznetsova A, Brockhoff PB, Christensen RHB. lmerTest Package: Tests in Linear Mixed Effects Models. J Stat Soft. 2017;82(13). doi: 10.18637/jss.v082.i13 [DOI] [Google Scholar]
  • 27.R Core Team (2018). R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. Accessed from: https://www.R-project.org/. [Google Scholar]
  • 28.Lüdecke D (2023). sjPlot: Data Visualization for Statistics in Social Science. R package version 2.8.14, https://CRAN.R-project.org/package=sjPlot. [Google Scholar]
  • 29.Hoffman L, Rovine MJ. Multilevel models for the experimental psychologist: Foundations and illustrative examples. Behav Res. 2007;39(1):101–117. doi: 10.3758/bf03192848 [DOI] [PubMed] [Google Scholar]
  • 30.Mass CJ, Hox JJ. The consequences of estimation in the presence of nonindependence: An example from multilevel modeling. Qual Quant. 2005;39(5):457–473. [Google Scholar]
  • 31.Hox JJ. Multilevel Analysis: Techniques and Applications. 2nd ed. Routledge; 2010. [Google Scholar]
  • 32.Baldwin SA, Berkeljon A, Atkins DC, Olsen JA, Nielsen SL. Rates of change in naturalistic psychotherapy: Contrasting dose–effect and good-enough level models of change. J Consult Clin Psychol. 2009;77(2):203–211. doi: 10.1037/a0015235 [DOI] [PubMed] [Google Scholar]
  • 33.Kendall PC, Peterman JS. CBT for Adolescents With Anxiety: Mature Yet Still Developing. AJP. 2015;172(6):519–530. doi: 10.1176/appi.ajp.2015.14081061 [DOI] [PubMed] [Google Scholar]
  • 34.Carpenter JK, Andrews LA, Witcraft SM, Powers MB, Smits JAJ, Hofmann SG. Cognitive behavioral therapy for anxiety and related disorders: A meta‐analysis of randomized placebo‐controlled trials. Depress Anxiety. 2018;35(6):502–514. doi: 10.1002/da.22728 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Olatunji BO, Cisler JM, Deacon BJ. Efficacy of Cognitive Behavioral Therapy for Anxiety Disorders: A Review of Meta-Analytic Findings. Psychiatr Clin North Am. 2010;33(3):557–577. doi: 10.1016/j.psc.2010.04.002 [DOI] [PubMed] [Google Scholar]
  • 36.van Dis EAM, van Veen SC, Hagenaars MA, Batelaan NM, Bockting CLH, van den Heuvel RM, et al. Long-term Outcomes of Cognitive Behavioral Therapy for Anxiety-Related Disorders: A Systematic Review and Meta-analysis. JAMA Psychiatry. 2020;77(3):265–273. doi: 10.1001/jamapsychiatry.2019.3986 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Springer KS, Levy HC, Tolin DF. Remission in CBT for adult anxiety disorders: A meta-analysis. Clin Psychol Rev. 2018;61:1–8. doi: 10.1016/j.cpr.2018.03.002 [DOI] [PubMed] [Google Scholar]
  • 38.DiMauro J, Domingues J, Fernandez G, Tolin DF. Long-term effectiveness of CBT for anxiety disorders in an adult outpatient clinic sample: A follow-up study. Behav Res Ther. 2013;51(2):82–86. doi: 10.1016/j.brat.2012.10.003 [DOI] [PubMed] [Google Scholar]
  • 39.Ettman CK, Abdalla SM, Cohen GH, Sampson L, Vivier PM, Galea S. Prevalence of Depression Symptoms in US Adults Before and During the COVID-19 Pandemic. JAMA Netw Open. 2020;3(9):e2019686. doi: 10.1001/jamanetworkopen.2020.19686 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Czeisler MÉ, Lane RI, Wiley JF, Czeisler CA, Howard ME, Rajaratnam SMW. Follow-up Survey of US Adult Reports of Mental Health, Substance Use, and Suicidal Ideation During the COVID-19 Pandemic, September 2020. JAMA Netw Open. 2021;4(2):e2037665. doi: 10.1001/jamanetworkopen.2020.37665 [DOI] [PMC free article] [PubMed] [Google Scholar]

Decision Letter 0

Mohammad Farris Iman Leong Bin Abdullah

4 Sep 2023

PONE-D-23-19350Response to Anxiety Treatment Before, During and After the COVID-19 PandemicPLOS ONE

Dear Dr. Rosmarin,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Please submit your revised manuscript by Oct 19 2023 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: https://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols.

We look forward to receiving your revised manuscript.

Kind regards,

Mohammad Farris Iman Leong Bin Abdullah, Dr Psych

Academic Editor

PLOS ONE

Journal requirements:

When submitting your revision, we need you to address these additional requirements.

1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at

https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and

https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

2. We note that you have stated that you will provide repository information for your data at acceptance. Should your manuscript be accepted for publication, we will hold it until you provide the relevant accession numbers or DOIs necessary to access your data. If you wish to make changes to your Data Availability statement, please describe these changes in your cover letter and we will update your Data Availability statement to reflect the information you provide.

3. Please amend either the title on the online submission form (via Edit Submission) or the title in the manuscript so that they are identical.

4. Please include your full ethics statement in the ‘Methods’ section of your manuscript file. In your statement, please include the full name of the IRB or ethics committee who approved or waived your study, as well as whether or not you obtained informed written or verbal consent. If consent was waived for your study, please include this information in your statement as well.

5. Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: I Don't Know

Reviewer #2: I Don't Know

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Please adding more relevant key words

Please consistently use same format in describing the dates such as July 1st 2020 throughout the article.

The result and discussion only highlighted about the efficacy of CBT for anxiety but in the methodology indicated that the respondents also received DBT.

Please mention how many sessions your respondents received and is there any standardized protocol to for your intervention. Please discuss the medium that you used in conducting your intervention.

Please explain how you compare the unequal group size and controlled the possible bias.

Reviewer #2: The role of CBT in anxiety treatment is an important area of research in mental health studies. The present article will add to the research in this area.

There are a few clarifications needed from the authors:

1. Was there uniformity of treatment in all groups? Did the "during pandemic" and "post pandemic " group receive any additional counselling, specific to the pandemic? Was their counselling more frequent?

2. The data in this study is of anxiety patients who adhered to treatment and completed it. There is no mention of any data of patients who had dropped out of treatment during the specified period. It would be pertinent to know the proportion of anxiety patients who started the treatment but did not complete it.

**********

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: No

**********

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

PLoS One. 2024 Mar 13;19(3):e0296949. doi: 10.1371/journal.pone.0296949.r002

Author response to Decision Letter 0


19 Sep 2023

Reviewer #1:

Please adding more relevant key words

- Thank you, we have added several key words.

Please consistently use same format in describing the dates such as July 1st 2020 throughout the article.

- We are grateful for this point, and have made the dates consistent throughout the manuscript.

The result and discussion only highlighted about the efficacy of CBT for anxiety but in the methodology indicated that the respondents also received DBT.

- CBT is a large conglomerate of therapy techniques that includes DBT. However, we appreciate Reviewer #1’s point and have mentioned these approaches separately in the paper.

Please mention how many sessions your respondents received and is there any standardized protocol to for your intervention. Please discuss the medium that you used in conducting your intervention.

- We have added the number of weekly sessions completed by each study group to Table 1. We have also clarified in the introduction and methods that patients presented to a naturalistic outpatient setting. Finally, we have added to the discussion that this feature of our study adds to the ecological validity of the findings.

Please explain how you compare the unequal group size and controlled the possible bias.

- Multilevel modeling is robust to unequal group sizes. We have added a brief comment to this effect at the start of the Statistical Analyses section.

Reviewer #2: The role of CBT in anxiety treatment is an important area of research in mental health studies. The present article will add to the research in this area.

- Thank you for these kind comments.

There are a few clarifications needed from the authors:

1. Was there uniformity of treatment in all groups? Did the "during pandemic" and "post

pandemic " group receive any additional counselling, specific to the pandemic? Was their

counselling more frequent?

- Our results suggest that groups received a similar number of sessions, relative to their aggregate time in therapy.

2. The data in this study is of anxiety patients who adhered to treatment and completed it. There is no mention of any data of patients who had dropped out of treatment during the specified period. It would be pertinent to know the proportion of anxiety patients who started the treatment but did not complete it.

- As above comments to Reviewer #1, we have added the number of treatment sessions completed by each group. Note that the naturalistic nature of our study precludes assessment of “drop-outs” since there was no fixed start or end point for treatment.

Attachment

Submitted filename: 20230913_Response.docx

pone.0296949.s001.docx (85.5KB, docx)

Decision Letter 1

Mohammad Farris Iman Leong Bin Abdullah

21 Dec 2023

Response to Anxiety Treatment Before, During, and After the COVID-19 Pandemic

PONE-D-23-19350R1

Dear Dr. Rosmarin,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

Kind regards,

Mohammad Farris Iman Leong Bin Abdullah, Dr Psych

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

Reviewer #2: All comments have been addressed

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: I Don't Know

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: (No Response)

Reviewer #2: All queries in previous version have been satisfactorily addressed by the authors. No further queries from this reviewer.

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: No

**********

Acceptance letter

Mohammad Farris Iman Leong Bin Abdullah

19 Feb 2024

PONE-D-23-19350R1

PLOS ONE

Dear Dr. Rosmarin,

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now being handed over to our production team.

At this stage, our production department will prepare your paper for publication. This includes ensuring the following:

* All references, tables, and figures are properly cited

* All relevant supporting information is included in the manuscript submission,

* There are no issues that prevent the paper from being properly typeset

If revisions are needed, the production department will contact you directly to resolve them. If no revisions are needed, you will receive an email when the publication date has been set. At this time, we do not offer pre-publication proofs to authors during production of the accepted work. Please keep in mind that we are working through a large volume of accepted articles, so please give us a few weeks to review your paper and let you know the next and final steps.

Lastly, if your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

If we can help with anything else, please email us at customercare@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Mohammad Farris Iman Leong Bin Abdullah

Academic Editor

PLOS ONE

Associated Data

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

    Supplementary Materials

    Attachment

    Submitted filename: 20230913_Response.docx

    pone.0296949.s001.docx (85.5KB, docx)

    Data Availability Statement

    Data are publicly available from OSF at https://osf.io/yusdk/.


    Articles from PLOS ONE are provided here courtesy of PLOS

    RESOURCES