Effectiveness of Predominantly Group Schema Therapy and Combined Individual and Group Schema Therapy for Borderline Personality Disorder: A Randomized Clinical Trial

Arnoud Arntz; Gitta A Jacob; Christopher W Lee; Odette Manon Brand-de Wilde; Eva Fassbinder; R Patrick Harper; Anna Lavender; George Lockwood; Ioannis A Malogiannis; Florian A Ruths; Ulrich Schweiger; Ida A Shaw; Gerhard Zarbock; Joan M Farrell

doi:10.1001/jamapsychiatry.2022.0010

. 2022 Mar 2;79(4):287–299. doi: 10.1001/jamapsychiatry.2022.0010

Effectiveness of Predominantly Group Schema Therapy and Combined Individual and Group Schema Therapy for Borderline Personality Disorder

A Randomized Clinical Trial

Arnoud Arntz ^1,^✉, Gitta A Jacob ², Christopher W Lee ³, Odette Manon Brand-de Wilde ⁴, Eva Fassbinder ^5,⁶, R Patrick Harper ⁷, Anna Lavender ⁸, George Lockwood ⁹, Ioannis A Malogiannis ¹⁰, Florian A Ruths ⁸, Ulrich Schweiger ⁵, Ida A Shaw ¹¹, Gerhard Zarbock ¹², Joan M Farrell ^11,¹³

¹Department of Clinical Psychology, University of Amsterdam, Amsterdam, the Netherlands

²Department of Clinical Psychology and Psychotherapy, Institute for Psychology, University of Freiburg, Freiburg, Germany

³Faculty of Health and Medical Sciences, University of Western Australia, Perth, Western Australia, Australia

⁴De Viersprong, the Netherlands Institute for Personality Disorders, Halsteren, the Netherlands

⁵Department of Psychiatry and Psychotherapy, University of Lübeck, Lübeck, Germany

⁶Department of Psychiatry and Psychotherapy, Christian-Albrechts University of Kiel, Kiel, Germany

⁷Bradford District Care NHS Foundation Trust, Bradford, United Kingdom

⁸South London and Maudsley NHS Foundation Trust, London, United Kingdom

⁹Schema Therapy Institute Midwest, Kalamazoo, Michigan

¹⁰First Department of Psychiatry, Eginition Hospital, Medical School, Athens University, Athens, Greece

¹¹Schema Therapy Institute Midwest, Indianapolis, Indiana

¹²Institut für Verhaltenstherapie Ausbildung Hamburg GmbH (Institute for Training in Cognitive Behavioral Therapy), Hamburg, Germany

¹³Department of Clinical Psychology, Indiana University–Purdue University, Indianapolis

Accepted for Publication: January 1, 2022.

Published Online: March 2, 2022. doi:10.1001/jamapsychiatry.2022.0010

^✉

Corresponding Author: Arnoud Arntz, PhD, Department of Clinical Psychology, University of Amsterdam, PO Box 15933, 1001 NK Amsterdam, the Netherlands (a.r.arntz@uva.nl).

Author Contributions: Dr Arntz had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

Concept and design: Arntz, Jacob, Brand-de Wilde, Harper, Lavender, Lockwood, Schweiger, Shaw, Farrell.

Acquisition, analysis, or interpretation of data: Arntz, Jacob, Lee, Brand-de Wilde, Fassbinder, Harper, Lavender, Malogiannis, Ruths, Schweiger, Zarbock.

Drafting of the manuscript: Arntz, Jacob, Lee, Fassbinder, Schweiger.

Critical revision of the manuscript for important intellectual content: All authors.

Statistical analysis: Arntz, Lee, Schweiger.

Obtained funding: Arntz, Jacob, Lee, Harper, Lavender, Farrell.

Administrative, technical, or material support: Arntz, Jacob, Lee, Brand-de Wilde, Fassbinder, Harper, Lavender, Lockwood, Ruths, Schweiger, Zarbock, Farrell.

Supervision: Jacob, Lee, Fassbinder, Lavender, Schweiger, Shaw, Farrell.

Conflict of Interest Disclosures: Dr Arntz reported receiving grants from the Netherlands Organization for Health Research and Development and Netherlands Foundation for Mental Health, and receiving other grants outside the submitted work from Netherlands’ Organization for Scientific Research (NWO), Netherlands Organization for Health Research and Development (ZONMW), Stichting Achmea Gezondheidszorg, CZ Fonds, Stichting Volksbond Rotterdam, and Stichting tot Steun VCVGZ; receiving royalties (paid to the university) from Academic Press, American Psychological Association Press, Beltz, Bohn Stafleu van Loghum, Boom Uitgevers, Cambridge University Press, Context Press, Guilford, De Tijdstroom, Oxford University Press, SAGE Publications, Uitgeverij Nieuwezijds, Wiley; providing workshops and lectures on cognitive behavioral therapy (CBT), imagery rescripting, personality disorders, schema therapy, and small-scale research in clinical practice (remuneration to the university) for the BABCP, Bulgarian Association for CBT, Clinical Academic Group for Psychotherapy Denmark, Danish Competence Centre for Psychotherapy, EABCT, ECNP, ESSPD, Estonian CBT Association, German Psychosomatic Congress, GGZ InGeest, Greek CBT Association, ICCP, Institut für Schematherapie Frankfurt, ISC International, ISSPD, ISST, Jellinek, Kenniscentrum Persoonlijkheidsstoornissen, Leiden University Medical Center, Lemion, Moroccan Association of CBT, Norwegian Psychological Association, Parnassia/PsyQ, Polish Association for Cognitive and Behavioural Therapies, Portuguese Association of Behaviour Therapy, Psyflix, SCEM, Scuole APC-SPC-SICC-IGB-AIPC, Tunisian Association of CBT, Turkish Association for Cognitive & Behavioral Psychotherapies, Ukraine Association for CBT, Ukraine Institute for CBT, University of Bordeaux, VGCT, VST, WCBCT; supervising research at the mental health institute PsyQ (remuneration to the University of Amsterdam); and being chair of the board of the PDO foundation, North Holland postgraduate training institute (unpaid). Dr Jacob reported receiving grants from the Else Kröner Fresenius-Stiftung; receiving grants from the German Research Foundation outside the submitted work; receiving personal fees for books from Beltz, Elsevier, Hogrefe, and Klett-Cotta; and receiving personal fees for workshops from Institute for Schema Therapy Hamburg, Institute for Schema Therapy Freiburg, Institute for Schema Therapy Cologne, Institute for Schema Therapy Bochum, Institute for Schema Therapy Berlin, CIP Akademie Munich, VTF Falkenried Hamburg, and NeST Institute for Schema Therapy Nuremberg. Dr Lee reported conducting training through Psychology Training; conducting workshops as part of the Australian Psychological Society Clinical College, EMDR international Association, Rural Doctors Association of Australia, International Society of Traumatic Stress Studies; having adjunct positions at the University of Western Australia and Murdoch University; receiving a Rotary Mental Health Grant for the current project and receiving a grant from Ramsay Health for research on depression; and being a board director for the Australian Psychological Society (paid) and for the WA PTSD Association (unpaid). Dr Brand-de Wilde reported having been employed at de Viersprong; having a (paid) freelance working affiliation with Jeugdhulp Friesland; being head of the psychotherapy training of RINO Amsterdam (paid); having an unpaid affiliation with the University of Amsterdam; being co-owner of Schematherapie in Bedrijf; being Managing Director of Treatment Affairs at Jeugdhulp Friesland; receiving royalties from Guilford Publications and Bohn Stafleu van Loghum and Boom Uitgevers; and receiving personal fees from providing lectures on (group) schema therapy, imagery rescripting, and personality disorders for EABCT, ISST, VGCT, VST, and Jeugdhulp Friesland. Dr Fassbinder reported receiving grants outside the submitted work from the Else Kröner-Fresenius-Stiftung, the University of Lübeck, and Addisca GmbH; receiving royalties from Beltz Verlag and Elsevier Books; receiving personal fees from supervision in schema therapy and group schema therapy and from workshops and presentations on CBT, imagery rescripting, personality disorders, schema therapy, and behavioral activation for Ausbildungsinstitut für Verhaltenstherapie und Verhaltensmedizin Hannover, Arbeitsgemeinschaft Wissenschaftliche Psychotherapie Berlin, the DGPPN, IPAM Marburg, IFT-Nord Institut für Therapie- und Gesundheitsforschung gemeinnützige GmbH Kiel, IPP Halle, Institut für Schematherapie Hamburg, Institut für Schematherapie Köln, Institut für Schematherapie Berlin, Oberberg Kliniken, and the WCBCT; and being co-chair of the Deutscher Fachverband für Verhaltenstherapie eV (unpaid). Mr Harper reported presenting workshops and trainings for Bradford District Care NHS Foundation Trust. Dr Lavender reported receiving royalty fees from Oxford University Press and Sage Publications outside the submitted work; receiving personal fees from teaching workshops on personality disorders from the Institute of Psychiatry, Psychology and Neuroscience and from Camden and Islington NHS Trust. Dr Lockwood reported presenting webinars for Schema Therapy Space and the Center for Cognitive Therapy, Russia on schema therapy (paid) and receiving personal fees for providing trainings in schema therapy for the Castle Wood Eating Disorders Treatment Center in California and for the State of Nebraska Department of Correctional Services. Dr Malogiannis reported receiving fees for providing workshops, training, and/or supervision for the Greek Society of Schema Therapy, the Institute of Behaviour Research and Therapy of Athens, Greece, and the S.A. (Limited Liability Company) of Cognitive and Behaviour Therapy Education, Athens, Greece, and receiving financial support for the study from the Institut für Verhaltenstherapie Ausbildung Hamburg. Dr Ruths reported being director of Elector Palatinate Ltd (paid); teaching at the Institute for Psychiatry Psychology and Neuroscience, King’s College London (unpaid); and receiving personal fees for teaching CBT including schema therapy for Solomons Tunbridge Wells (UK), Global Mental Health Institute for Public Health Heidelberg (Germany), and OdNova Gabinety Psychoterapeutyczne spółka cywilna (Poland). Dr Schweiger reported receiving royalty fees from Beltz, Herder, Hogrefe, Kohlhammer, and Springer; fees for workshops for Institutes associated with the Deutsche Fachverband für Verhaltenstherapie on psychotherapy topics; and being Vice President of the Deutsche Fachverband für Verhaltenstherapie (no honorarium). Ms Shaw and Dr Farrell reported being co-directors of the Schema Therapy Institute Midwest–Indianapolis; providing training and supervision for professional fees for the National University of Ireland, Idaho State Drug Court Treatment Program, Spalding University Forensic Track, Murdoch University, Perth, Australia, de Viersprong PD Institute, Clienia Littenheid Switzerland, IVAH Hamburg, University of Indianapolis, IPST_MZ Institute, Schema Therapy Institute New York, Van Genderen Opleidingen, Singapore Prison System, New Jersey Schema Therapy Institute, Leiden University, Swedish Institute CBT & ST, Stockholm, Istituto di Scienze Cognitive, Moscow Institute of Schema Therapy, St. Petersburg ST Institute, Greek Schema Society, Danish ST Institute, Norwegian STI, London Schema Therapy Institute, Japanese Society Schema Therapy, Schema Therapy Institute Australia, Schema Therapy Institute Hamburg, Schema Therapy Institute Frankfurt, Schema Therapy Institute Prague, Hungarian Schema Therapy Society; receiving honoraria for presentations from the International Society of Schema Therapy and Australian Psychological Association; and receiving royalties from Wiley-Blackwell and Guilford Press for writing books. Ms. Shaw reported receiving fees from Groningen University for supervising a grant-funded study. Dr Farrell reported receiving an honorarium as a visiting professor at St. Petersburg Polytechnical University. Dr Zarbock reported receiving personal fees from Beltz Verlag for publications, and from IVAH gGmbH (Germany), DGPPN Berlin (Germany), ISST St. Petersburg (Russia) for teaching. No other disclosures were reported.

Funding/Support: The sites in the Netherlands were supported by ZonMW grant 80-82310-97-12142 from the Netherlands Organization for Health Research and Development (Dr Arntz) and grant 2008 6350 from the Netherlands Foundation for Mental Health (Dr Arntz). The sites in Germany were supported by Else Kröner-Fresenius-Stiftung (Dr Jacob). The sites in Australia were supported by Australian Rotary Health (Dr Lee). The site in Greece was supported by the Greek Society of Schema Therapy, the First Department of Psychiatry of the Medical School of the University of Athens, and the Institut für Verhaltenstherapie Ausbildung Hamburg. The site in London, UK, was supported by the South London and Maudsley NHS Foundation Trust and by Research Center Experimental Psychopathology, Maastricht University. The site in Bradford, UK, was supported by the Bradford District Care NHS Foundation Trust.

Role of the Funder/Sponsor: The funders had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.

Data Sharing Statement: See Supplement 3.

Additional Contributions: We thank all patients, site coordinators, research assistants, students, and therapists for their contributions to the study. Michelle van de Glind-Houben, MSc, and Astrid van den Bosch of Maastricht University provided central research assistance, and Rosanne Janssen, MSc, of Maastricht University developed an online data collection system. They received no compensation outside their salary.

^✉

Corresponding author.

PMCID: PMC8892362 PMID: 35234828

This randomized clinical trial examines whether schema therapy is more effective than optimal treatment as usual for borderline personality disorder and whether it is more effectively delivered in a predominantly group or combined individual and group format.

Key Points

Question

Is group schema therapy for borderline personality disorder (BPD) more effective than optimal treatment as usual, and is predominantly group schema therapy or combined individual and group schema therapy more effective?

Findings

In this randomized clinical trial, which included 495 adult participants with BPD in 5 countries, combined individual and group schema therapy was significantly more effective than optimal treatment as usual and predominantly group schema therapy in reducing BPD severity.

Meaning

The findings add to the evidence for the effectiveness of schema therapy for BPD and indicate that the combination of individual and group schema therapy is the more effective schema therapy format.

Abstract

Importance

Schema therapy (ST), delivered either in an individual or group format, has been compared with other active treatments for borderline personality disorder (BPD). To our knowledge, the 2 formats have not been compared with treatment as usual (TAU) or with each other. Such comparisons help determine best treatment practices.

Objective

To evaluate whether ST is more effectively delivered in a predominantly group or combined individual and group format and whether ST is more effective than optimal TAU for BPD.

Design, Setting, and Participants

In this multicenter, 3-arm randomized clinical trial conducted at 15 sites in 5 countries (Australia, Germany, Greece, the Netherlands, and the UK), outpatients aged 18 to 65 years who had BPD were recruited between June 29, 2010, and May 18, 2016, to receive either predominantly group ST (PGST), combined individual and group ST (IGST), or optimal TAU. Data were analyzed from June 4, 2019, to December 29, 2021.

Interventions

At each site, cohorts of 16 to 18 participants were randomized 1:1 to PGST vs TAU or IGST vs TAU. Both ST formats were delivered over 2 years, with 2 sessions per week in year 1 and the frequency gradually decreasing during year 2. Assessments were collected by blinded assessors.

Main Outcomes and Measures

The primary outcome was the change in BPD severity over time, assessed with the Borderline Personality Disorder Severity Index (BPDSI) total score. Treatment retention was analyzed as a secondary outcome using generalized linear mixed model survival analysis.

Results

Of 495 participants (mean [SD] age, 33.6 [9.4] years; 426 [86.2%] female), 246 (49.7%) received TAU, 125 (25.2%) received PGST, and 124 (25.0%) received IGST (1 of whom later withdrew consent). PGST and IGST combined were superior to TAU with regard to reduced BPD severity (Cohen d, 0.73; 95% CI, 0.29-1.18; P < .001). For this outcome, IGST was superior to TAU (Cohen d, 1.14; 95% CI, 0.57-1.71; P < .001) and PGST (Cohen d, 0.84; 95% CI, 0.09-1.59; P = .03), whereas PGST did not differ significantly from TAU (Cohen d, 0.30; 95% CI, −0.29 to 0.89; P = .32). Treatment retention was greater in the IGST arm than in the PGST (1 year: 0.82 vs 0.72; 2 years: 0.74 vs. 0.62) and TAU (1 year: 0.82 vs 0.73; 2 years: 0.74 vs 0.64) arms, and there was no significant difference between the TAU and PGST arms (1 year: 0.73 vs 0.72; 2 years: 0.64 vs 0.62).

Conclusions and Relevance

In this randomized clinical trial, IGST was more effective and had greater treatment retention compared with TAU and PGST. These findings suggest that IGST is the preferred ST format, with high retention and continuation of improvement in BPD severity after the completion of treatment.

Trial Registration

trialregister.nl Identifier: NTR2392

Introduction

Meta-analytic reviews have found specialized therapies for borderline personality disorder (BPD) to be associated with greater reductions in overall BPD severity than treatment as usual (TAU).^1,2 One specialized therapy is schema therapy (ST). Early trials of ST demonstrated effectiveness when delivered in an individual format.^3,4 A large effect was found for group ST delivered as an adjunct to TAU.⁵ However, this group ST was delivered by its developers, and therefore, the generalizability of this finding to other therapists and other settings was unclear. Also unknown was the extent to which group ST would be effective as a stand-alone treatment and the relative merits of combining individual and group ST.

An international workgroup, in considering these issues, speculated that the group-only format might encourage patients to bring all issues to the group, thus optimizing group therapeutic processes. Conversely, an argument was made that combining individual with group ST would better meet patients’ needs for attention and attachment and better facilitate the processing of severe childhood adverse experiences, a hallmark of ST.^6,7 The workgroup decided to test these competing positions through an international randomized clinical trial (RCT) with 3 arms: predominantly group ST (PGST), combined individual and group ST (IGST), and TAU.⁸ We decided to use optimal TAU as a comparator—that is, the optimal treatment that was available at the treatment site according to the usual local practice (excluding ST).

This RCT examined the effectiveness of ST in 2 formats compared with optimal TAU and also compared the effectiveness of the 2 ST formats. We investigated effectiveness for the primary outcome measure (BPD severity). Secondary outcomes included treatment retention, specific BPD and general psychiatric symptoms, quality of life, schemas and schema modes, and psychosocial functioning. We report the results of the planned analyses⁸: first, both group ST formats were combined and compared with TAU, and then the 3 arms were compared with each other. The first hypothesis was that the 2 ST formats combined would be superior to TAU in reducing BPD severity. The second hypothesis was that the 3 treatment types would differ in effectiveness. Moreover, we explored differences in treatment retention and other secondary outcomes.

Methods

Study Design

This international multicenter RCT had 3 arms: optimal TAU, PGST, and IGST. Participants were randomized 1:1 in cohorts of 16 to 18 participants per site either to PGST or TAU or to IGST or TAU (NTR2392) (trial protocol in Supplement 1). The order of these cohort types was randomly assigned across sites. There were 15 sites: 2 in Australia, 3 in Germany, 1 in Greece, 7 in the Netherlands, and 2 in the UK (details are provided in eAppendix 1 in Supplement 2). Because some sites could not finance participation or recruit a second cohort, other sites compensated by including extra cohorts, deviating from the plan⁸ (eAppendix 2 in Supplement 2). The number of cohorts per site varied from 1 to 5. Thirty cohorts were recruited. The mean rank order of cohort type (PGST vs IGST) was equal (eAppendix 1 in Supplement 2). The planned minimum number of participants was 448 from 28 cohorts based on a power analysis (power 90%; medium effect size, α = 0.05) and taking attrition into account.⁸ Ethical approval was obtained at each participating site. Participants provided written informed consent. This study followed the Consolidated Standards of Reporting Trials (CONSORT) reporting guideline.

Patients

Participants were recruited between June 29, 2010, and May 18, 2016. Figure 1 shows the CONSORT flow diagram; 495 patients were randomly assigned, 1 withdrew consent, and 494 were analyzed. Inclusion criteria were a primary diagnosis of BPD, age of 18 to 65 years, a Borderline Personality Disorder Severity Index IV (BPDSI-IV) score greater than 20 (range, 0-90; a score >20 denotes clear BPD; 15 is the cutoff for BPD, and <15 is used as recovery criterion), and the willingness and ability to participate in 2 years of treatment. Exclusion criteria were an inability to speak, read, and/or understand the study site’s language, an IQ less than 80, a psychotic disorder (except reactive episodes; BPD criterion 9 per the DSM-5), bipolar disorder 1, dissociative identity disorder, untreated attention-deficit/hyperactivity disorder, addiction needing clinical detoxification (inclusion after detoxification was allowed), full or subthreshold narcissistic or antisocial PD, a serious and/or unstable medical illness, and having received ST for more than 3 months during the previous 3 years. Ethnicity was self-reported. Diagnoses were made with the Structured Clinical Interview for DSM-IV Axis I and II Disorders. Sites were eligible if they offered treatment for BPD, had therapists willing to be trained in group ST, agreed to adhere to the study protocol, and could organize and finance the study.

Randomization and Masking

When a cohort of 16 to 18 participants was accrued, participants of that cohort were randomly assigned by a central independent research assistant using computerized randomization in blocks of 2 based on the order of completion of baseline assessments. The type of ST (PGST or IGST) per cohort was randomized across sites.⁸ Assessors were blinded to the condition. The study blind was removed after the last data became available. Given the unequal sample sizes in the 3 arms, blinding during analysis was not feasible.

Procedures

Treatments and Therapists

Group ST followed a protocol.^9,10 In PGST, 2 group sessions per week were provided in year 1, with a maximum of 12 individual sessions available on patient request. In year 2, group ST was provided once per week in months 13 to 18, once per 2 weeks in months 19 to 21, and once monthly in months 22 to 24, with a maximum of 5 individual ST sessions available on request.

For IGST, 2 sessions (1 individual^7,10 and 1 group) per week were delivered in year 1. In the first 6 months of year 2 (months 13 to 18), frequencies of both individual and group ST were biweekly. In months 19 to 21, group ST was provided biweekly and individual ST was provided monthly. In months 22 to 24, both were offered monthly (details are shown in eTable 1 in Supplement 2).

Group ST was closed and provided by 2 therapists. For IGST, most patients had an individual therapist other than their group therapists. All ST therapists were licensed mental health professionals trained in individual ST for BPD. Group ST therapists were additionally trained by I.S. and J.F.⁹ Initially, therapists in both ST formats received online supervision by I.S. weekly; after 6 months, supervision was reduced to biweekly or monthly depending on the therapists’ experience.

Treatment as usual was the optimal psychological treatment available at the site. The most frequently offered was dialectical behavior therapy, with an intensity matched to that of ST. An overview of the types of TAU offered is shown in eTable 2 in Supplement 2.

Treatment Integrity and Assessments

A scale was designed to assess whether ST discriminated from TAU (eAppendix 3 in Supplement 2). Independent evaluators rated the quality of individual and group ST.¹¹ There were 6 face-to-face assessments: at baseline and at 6, 12, 18, 24, and 36 months.

Outcomes

The primary outcome was the slope over time of BPD severity during the past 3 months as assessed at baseline, 6 months, 12 months, 18 months, 24 months, and 36 months with the BPDSI-IV total score, a reliable and valid index of BPD severity.¹² Secondary outcomes included 9 BPDSI subscales (representing the BPD criteria); suicidality and the number of suicide attempts during the past 3 months, assessed with the BPDSI-IV; the BPD Checklist¹³ (assessing the self-reported burden of BPD manifestations); Global Assessment of Functioning (DSM-III) and Social and Occupational Functioning Assessment Scale¹⁴ ratings, based on semistructured interviews⁸; the Brief Symptom Inventory¹⁵ (general psychopathology symptoms); the Work and Social Adjustment Scale¹⁶ (work and social functioning); the World Health Organization Quality of Life assessment¹⁷; a happiness item⁸; the Young Schema Questionnaire–short form¹⁸; the Schema Mode Inventory¹⁹ (providing 2 scores, 1 for dysfunctional and 1 for functional schema modes); and having employment or being a student. eAppendix 4 in Supplement 2 provides details on the instruments used. We assessed treatment retention because previous studies found a low rate of dropout from ST.^3,5,20

Statistical Analysis

Data were analyzed from June 4, 2019, to December 29, 2021. Given skewed distributions, the BPDSI total and subscale scores were analyzed with generalized linear mixed model (GLMM) gamma regression with a log link, with random effects of treatment for site and of treatment and time for the cohort nested under the site if estimation allowed (eAppendix 5 in Supplement 2). For the repeated part, an autoregressive moving average (1,1) model was used. The fixed part contained time, treatment, and their interaction, with the time × treatment interaction (the difference in slopes) testing the differential effectiveness hypothesis. Because gamma regression cannot be conducted with 0, a small value (0.01) was added to scores. Sensitivity analyses were performed to test the robustness of this choice. Effect sizes were expressed as r = √(t²/[t² + df]) for fixed effects, and Cohen d was the conventional effect size, with the numerator based on estimated means from GLMM gamma regression and the denominator as baseline SD in transformed scale (based on GLMM gamma regression with a log link, without random parts, and with an intercept for the fixed part) (eAppendix 6 in Supplement 2). Treatment retention was analyzed using GLMM survival analysis of treatment dropout per quarter (every 3 months) during 2 years with the site as a random intercept. The number of suicide attempts during the previous 3 months was analyzed using generalized estimating equations with a Tweedie distribution (because of many 0 counts) with a log link and first-order autoregression for the repeated part. Depending on the distribution, secondary outcomes not based on the BPDSI were analyzed with appropriate LMM or GLMM. The time model was either linear or piecewise (if an inflection point was observed in all at 1 year). The choice of a piecewise model was supported by superior fit, tested with χ² tests. For all piecewise models, the time × treatment interaction was not significant and did not lead to improved fit; thus, it was deleted, implicating that treatment effects were assessed by the difference in slopes in years 2 and 3. In accordance with the preset plan,⁸ first, both ST formats were jointly compared with TAU; next, the 3 arms were compared. Binomial tests (with a probability of 0.05) were used to assess the likelihood of the number of significant tests of secondary outcomes per comparison.²¹ Analyses were conducted in SPSS, version 25 (IBM), as intention-to-treat after the last data became available. Significance was set at 2-tailed P = .05. Different sample sizes made blind analysis impossible.

Results

A total of 495 patients participated in the study (mean [SD] age, 33.6 [9.4] years; range, 18.6-61.7 years; 426 [86.2%] female). Of these, 246 (49.7%) received TAU, 125 (25.2%) received PGST, and 124 (25.0%) received IGST (1 of whom later withdrew consent). Table 1 shows baseline descriptive statistics for the participants.

Table 1. Descriptive Statistics at Baseline and Treatment Integrity Test Results.

Characteristic	Patients^a
Characteristic	TAU arm (n = 246)	PGST arm (n = 125)	IGST arm (n = 123)
Age, mean (SD), y	33.89 (9.55)	33.20 (9.33)	33.46 (9.17)
Sex
Female	212 (86.2)	109 (87.2)	105 (85.4)
Male	33 (13.4)	16 (12.8)	17 (13.8)
Other or unknown	1 (0.4)	0 (0)	1 (0.8)
Relationship status
Partner	99 (40.2)	41 (32.8)	41 (33.3)
No partner	147 (59.8)	84 (67.2)	82 (66.7)
Educational level, mean (SD)^b	3.2 (1.6)	3.4 (1.6)	3.4 (1.7)
Ethnicity
Same as dominant group at study site	230 (93.5)	118 (94.4)	106 (86.2)
Different from dominant group at study site	16 (6.5)	7 (5.6)	17 (13.8)
Employment status^c
Employed	79 (32.2)	34 (27.2)	34 (27.9)
Homemaker	16 (6.5)	6 (4.8)	7 (5.7)
Student	26 (10.6)	13 (10.4)	8 (6.6)
Disability or illness benefit	95 (38.8)	59 (47.2)	49 (40.2)
Unemployed	29 (11.8)	13 (10.4)	24 (19.7)
GAF score, mean (SD)	49.70 (8.69)	50.09 (8.10)	48.36 (8.32)
BPD severity
BPD criteria (SCID-II), mean (SD), No.	6.83 (1.33)	7.05 (1.38)	6.81 (1.30)
BPDSI total score, mean (SD)	31.63 (8.60)	30.95 (8.75)	30.44 (8.74)
Comorbid disorders
DSM-IV Axis I diagnoses (SCID-I), mean (SD), No.	3.31 (2.15)	3.57 (2.13)	3.76 (2.23)
DSM-IV Axis II diagnoses (SCID-II), mean (SD), No.^d	1.74 (1.04)	1.87 (1.01)	1.76 (1.02)
PD
Avoidant	77 (31.3)	37 (29.6)	47 (38.2)
Dependent	20 (8.1)	10 (8.0)	14 (11.4)
Obsessive-compulsive	38 (15.4)	19 (15.2)	18 (14.6)
Paranoid	48 (19.5)	21 (16.8)	27 (22.0)
Schizotypal	3 (1.2)	1 (0.8)	0 (0)
Schizoid	1 (0.4)	3 (2.4)	1 (0.8)
Histrionic	0 (0)	1 (0)	0 (0)
Conduct disorder youth	52 (21.1)	33 (26.4)	26 (21.1)
Antisocial A^e	2 (0.8)	1 (0.8)	4 (3.3)
TIS rating, mean (SE)^f
Nonspecific subscale	50.69 (0.93)^g	53.76 (1.19)	54.85 (1.16)
Specific subscale	39.21 (0.86)^g	48.18 (1.13)	50.68 (1.09)
Non-ST subscale	4.74 (0.11)	4.47 (0.15)	4.77 (0.15)

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Abbreviations: BPD, borderline personality disorder; BPDSI, Borderline Personality Disorder Severity Index; GAF, Global Assessment of Functioning; IGST, combination of individual and group schema therapy; PD, personality disorder; PGST, predominantly group schema therapy; SCID-I, Structured Clinical Interview for DSM-IV Axis I Disorders; SCID-II, Structured Clinical Interview for DSM-IV Axis II Disorders; ST, schema therapy; TAU, (optimal) treatment as usual; TIS, therapy integrity scale.

^{^a}

Data are presented as the number (percentage) of patients unless otherwise indicated.

^{^b}

Based on the International Standard Classification of Education, 2011 version, with a range of 0 to 8.

^{^c}

Two patients had missing responses (1 from the TAU group and 1 from the IGST group).

^{^d}

Included BPD.

^{^e}

Full antisocial PD was an exclusion criterion, as was narcissistic PD.

^{^f}

Means and SEs were from mixed regression of the TIS ratings at 6, 12, 18, and 24 months.

^{^g}

The TAU group had significantly lower TIS scores than did the ST groups (TAU vs PGST: d, 0.34; TAU vs IGST: d, 0.90; P < .001); scores from the PGST and IGST groups did not differ significantly from each other. Analyzed with linear mixed models with treatment and time in the fixed part, random intercept and slope for time for cohort within site, and autoregressive moving average (1,1) covariance for the repeated part.

Assessment of Treatment Integrity

The Treatment Integrity Scale discriminated ST from TAU (Table 1). The quality of individual and group ST was rated between good and very good by independent raters¹¹ (eAppendix 3 in Supplement 2).

Primary Outcomes

Forty-two recordings of BPDSI interviews were randomly selected; these were rated by an independent assessor, and the BPDSI total scores were then compared with those reported by the original interviewer. Interrater agreement was excellent (intraclass correlation coefficient, 0.99).

For reduction of the total BPDSI-IV score, IGST and PGST combined were superior to TAU, with a medium to large effect size (Cohen d, 0.73; 95% CI, 0.29-1.18; P = .001) (Table 2 and Table 3). The difference was significant at 1.5 years (mean [SE] difference, 2.38 [0.98]; 95% CI, 0.27-4.49; P = .03).

Table 2. Estimated Means, 95% CIs, and Effect Sizes for the Primary and Secondary Outcomes.

Outcome, time, y	Effect size
	TAU		PGST		IGST
	Estimated mean (95% CI)^a	Cohen d^b	Estimated mean (95% CI)^a	Cohen d^b	Estimated mean (95% CI)^a	Cohen d^b
Primary outcome
BPDSI total score
Baseline	30.69 (28.45-33.11)	NA	30.14 (27.44-33.10)	NA	30.51 (27.80-33.49)	NA
0.5	27.46 (25.51-29.56)	0.40	26.59 (24.33-29.06)	0.45	25.90 (23.72-28.28)	0.59
1.0	24.57 (22.77-26.51)	0.80	23.47 (21.42-25.71)	0.90	21.98 (20.10-24.05)	1.18
1.5	21.98 (20.22-23.89)	1.20	20.71 (18.71-22.92)	1.35	18.66 (16.90-20.60)	1.77
2.0	19.67 (17.87-21.64)	1.60	18.27 (16.24-20.56)	1.80	15.84 (14.13-17.75)	2.36
3.0	15.74 (13.84-17.90)	2.41	14.23 (12.12-16.70)	2.70	11.41 (9.78-13.31)	3.55
Secondary outcomes
BPD checklist
Baseline	67.04 (61.47-73.12)	NA	68.95 (61.01-77.92)	NA	64.43 (57.01-72.81)	NA
0.5	60.31 (55.50-65.53)	0.24	60.93 (54.23-68.45)	0.28	56.08 (49.93-63.00)	0.31
1.0	54.23 (49.76-59.16)	0.47	53.84 (47.80-60.66)	0.55	48.82 (43.38-54.94)	0.62
1.5	48.81 (44.31-53.77)	0.71	47.58 (41.77-54.20)	0.83	42.50 (37.39-48.30)	0.93
2.0	43.91 (39.25-49.17)	0.95	42.05 (36.26-48.77)	1.11	36.99 (32.02-42.74)	1.24
3.0	35.54 (30.54-41.36)	1.42	32.84 (26.98-39.98)	1.66	28.03 (23.19-33.89)	1.86
GAF
Baseline	51.06 (48.42-53.71)	NA	50.87 (47.72-54.03)	NA	48.78 (45.65-51.91)	NA
0.5	53.04 (50.46-55.63)	0.23	53.22 (50.17-56.27)	0.28	51.70 (48.68-54.73)	0.35
1.0	55.03 (52.42-57.63)	0.47	55.57 (52.50-58.63)	0.55	54.62 (51.59-57.65)	0.69
1.5	57.01 (54.32-59.70)	0.70	57.91 (54.72-61.10)	0.83	57.54 (54.40-60.68)	1.04
2.0	58.99 (56.15-61.83)	0.94	60.26 (56.84-63.68)	1.11	60.46 (57.11-63.81)	1.38
3.0	62.95 (59.62-66.28)	1.41	64.95 (60.82-69.09)	1.66	66.30 (62.29-70.32)	2.07
SOFAS
Baseline	51.86 (49.36-54.36)	NA	51.30 (48.27-54.34)	NA	49.44 (46.43-52.45)	NA
0.5	53.78 (51.32-56.23)	0.21	53.83 (50.88-55.77)	0.28	52.18 (49.26-55.10)	0.30
1.0	55.69 (53.19-58.19)	0.42	56.35 (53.35-59.35)	0.56	54.92 (51.97-57.88)	0.61
1.5	57.61 (54.97-60.25)	0.64	58.87 (55.69-62.06)	0.84	57.67 (54.54-60.80)	0.91
2.0	59.52 (56.66-62.39)	0.85	61.40 (57.91-64.88)	1.12	60.41 (57.00-63.83)	1.21
3.0	63.36 (59.84-66.88)	1.27	66.44 (62.09-70.80)	1.68	65.90 (61.66-70.14)	1.82
WSAS
Baseline	23.23 (21.75-24.82)	NA	23.55 (21.52-25.78)	NA	23.54 (21.51-25.76)	NA
0.5	20.53 (19.24-21.90)	0.33	20.81 (19.04-22.75)	0.33	20.80 (19.04-22.72)	0.33
1.0	18.14 (16.77-19.61)	0.66	18.39 (16.66-20.30)	0.66	18.38 (16.67-20.26)	0.66
1.5	17.43 (16.03-18.95)	0.77	16.82 (15.18-18.65)	0.90	16.92 (15.28-18.73)	0.88
2.0	16.75 (15.17-18.49)	0.87	15.39 (13.64-17.37)	1.14	15.57 (13.83-17.53)	1.10
3.0	15.46 (13.39-17.85)	1.09	12.88 (10.76-15.42)	1.61	13.19 (11.10-15.68)	1.55
WHO QOL
Baseline	70.62 (65.42-75.83)	NA	69.46 (62.07-76.86)	NA	71.05 (63.66-78.45)	NA
0.5	75.29 (70.10-80.49)	0.26	74.14 (66.75-81.52)	0.26	75.73 (68.34-83.11)	0.26
1.0	81.45 (76.05-86.85)	0.51	80.60 (73.07-88.13)	0.51	83.82 (76.30-91.33)	0.51
1.5	81.45 (76.05-86.85)	0.60	80.60 (73.07-88.13)	0.61	83.82 (76.30-91.33)	0.70
2.0	82.93 (77.34-88.53)	0.68	82.39 (74.65-90.12)	0.71	87.24 (79.54-94.94)	0.89
3.0	85.90 (79.59-92.21)	0.84	85.97 (77.37-94.56)	0.91	94.08 (85.60-102.56)	1.27
BSI
Baseline	1.86 (1.73-2.01)	NA	1.99 (1.81-2.18)		1.85 (1.69-2.03)	NA
0.5	1.66 (1.54-1.79)	0.30	1.77 (1.61-1.94)	0.30	1.65 (1.50-1.80)	0.30
1.0	1.48 (1.36-1.60)	0.60	1.58 (1.43-1.74)	0.60	1.46 (1.33-1.61)	0.60
1.5	1.40 (1.29-1.52)	0.74	1.45 (1.31-1.60)	0.81	1.32 (1.19-1.45)	0.87
2.0	1.33 (1.21-1.46)	0.88	1.34 (1.19-1.50)	1.03	1.19 (1.06-1.32)	1.15
3.0	1.19 (1.05-1.35)	1.16	1.13 (0.97-1.33)	1.45	0.96 (0.83-1.12)	1.69
YSQ
Baseline	55.82 (54.03-57.61)	NA	56.38 (53.89-58.88)	NA	56.55 (54.05-59.05)	NA
0.5	51.79 (50.02-53.55)	0.40	52.34 (49.87-54.82)	0.40	52.51 (50.04-54.98)	0.40
1.0	47.75 (45.83-49.66)	0.81	48.30 (45.72-50.88)	0.81	48.47 (45.92-51.03)	0.81
1.5	46.68 (44.76-48.61)	0.92	46.49 (43.91-49.06)	0.99	46.07 (43.51-48.62)	1.05
2.0	45.62 (43.55-47.70)	1.02	44.67 (41.91-47.43)	1.17	43.66 (40.94-46.34)	1.29
3.0	43.50 (40.81-46.19)	1.23	41.03 (37.45-44.62)	1.54	38.85 (35.38-42.31)	1.77
SMI-dysfunctional
Baseline	48.98 (47.90-50.06)	NA	49.54 (48.04-51.03)	NA	48.88 (47.39-50.38)	NA
0.5	45.79 (44.73-46.85)	0.44	46.35 (44.87-47.82)	0.44	45.69 (44.23-47.16)	0.44
1.0	42.60 (41.41-43.79)	0.88	43.16 (41.59-44.73)	0.88	42.51 (40.95-44.06)	0.88
1.5	41.73 (40.54-42.93)	0.99	41.90 (40.35-43.46)	1.05	40.90 (39.36-42.43)	1.10
2.0	40.87 (39.54-42.19)	1.11	40.65 (38.93-42.37)	1.22	39.28 (37.60-40.97)	1.32
3.0	39.13 (37.29-40.97)	1.35	38.15 (35.74-40.56)	1.56	36.06 (33.76-38.37)	1.76
SMI-functional
Baseline	5.73 (5.52-5.93)	NA	5.70 (5.41-5.99)	NA	5.66 (5.37-5.95)	NA
0.5	6.18 (5.97-6.38)	0.35	6.15 (5.87-6.44)	0.35	6.11 (5.83-6.40)	0.35
1.0	6.63 (6.49-6.86)	0.71	6.60 (6.30-6.90)	0.71	6.57 (6.27-6.86)	0.71
1.5	6.73 (6.50-6.97)	0.79	6.75 (6.45-7.06)	0.83	6.82 (6.52-7.12)	0.91
2.0	6.84 (6.58-7.09)	0.87	6.90 (6.57-7.24)	0.94	7.08 (6.75-7.41)	1.11
3.0	7.05 (6.70-7.39)	1.03	7.21 (6.76-7.65)	1.18	7.59 (7.16-8.02)	1.51
Happiness
Baseline	3.08 (2.92-3.25)	NA	2.90 (2.68-3.13)	NA	3.16 (2.94-3.39)	NA
0.5	3.42 (3.26-3.58)	0.30	3.24 (3.02-3.46)	0.30	3.50 (3.38-3.72)	0.30
1.0	3.76 (3.60-3.93)	0.59	3.57 (3.34-3.81)	0.59	3.83 (3.60-4.06)	0.59
1.5	3.81 (3.64-3.98)	0.64	3.75 (3.52-3.98)	0.75	3.94 (3.72-4.16)	0.69
2.0	3.87 (3.69-4.05)	0.69	3.93 (3.81-4.29)	0.91	4.05 (3.81-4.29)	0.78
3.0	3.98 (3.74-4.23)	0.79	4.28 (3.94-4.62)	1.22	4.26 (3.94-4.58)	0.97
Working/studying proportion
Baseline	0.42 (0.31-0.54)	NA	0.38 (0.26-0.51)	NA	0.34 (0.23-0.48)	NA
0.5	0.42 (0.31-0.53)	−0.01	0.40 (0.28-0.53)	0.09	0.37 (0.25-0.50)	0.09
1.0	0.41 (0.31-0.53)	−0.02	0.42 (0.30-0.56)	0.18	0.39 (0.27-0.52)	0.18
1.5	0.41 (0.30-0.53)	−0.03	0.44 (0.31-0.58)	0.28	0.41 (0.29-0.55)	0.28
2.0	0.41 (0.29-0.54)	−0.04	0.47 (0.32-0.61)	0.37	0.43 (0.30-0.58)	0.37
3.0	0.41 (0.28-0.55)	−0.05	0.51 (0.34-0.68)	0.55	0.48 (0.32-0.64)	0.55

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Abbreviations: BPD, borderline personality disorder; BPDSI, Borderline Personality Disorder Severity Index; BSI, Brief Symptom Inventory; GAF, Global Assessment of Functioning; IGST, combination of individual and group schema therapy; NA, not applicable; PGST, predominantly group schema therapy; SMI, Schema Mode Inventory; SOFAS, Social and Occupational Functioning Assessment Scale; TAU, (optimal) treatment as usual; WSAS, Work and Social Adjustment Scale; WHO QOL, World Health Organization Quality of Life assessment; YSQ, Young Schema Questionnaire–short form.

^{^a}

Estimated means and 95% CIs are in original scale.

^{^b}

Cohen d values are based on the parameters of the generalized linear mixed model analyses (change over time), with the square root of the baseline variance of a model with no random parts and only a fixed intercept as the denominator (ie, SD baseline in transformed scale).

Table 3. Comparison of Time Effects for First and Secondary Outcomes Between the ST Groups Combined vs the TAU Group, the PGST Group vs the TAU Group, the IGST Group vs the TAU Group, and the IGST Group vs the PGST Group^a.

Outcome, comparison	Time effects, slope over 3 y
Outcome, comparison	t	df	P	Cohen d (95% CI)^b	r
Primary outcome
Borderline Personality Disorder Severity Index total score
Main time effect	14.11	31	<.001	2.76 (2.36 to 3.16)	0.93
Time × treatment
ST vs TAU^c	3.24	1028	<.001	0.73 (0.29 to 1.18)	0.10
PGST vs TAU	0.99	924	.32	0.30 (−0.29 to 0.89)	0.03
IGST vs TAU^c	3.95	916	<.001	1.14 (0.57 to 1.71)	0.13
IGST vs PGST^c	2.21	491	.03	0.84 (0.09 to 1.59)	0.10
Secondary outcomes
Borderline personality disorder checklist^d
Main time effect	11.33	31	<.001	1.59 (1.30 to 1.85)	0.90
Time × treatment
ST vs TAU^c	2.03	910	.04	0.33 (0.00 to 0.67)	0.07
PGST vs TAU	1.05	763	.30	0.24 (–0.69 to 0.21)	0.04
IGST vs TAU^c	2.03	777	.04	0.44 (0.44 to 0.87)	0.07
IGST vs PGST	0.71	377	.48	0.20 (–0.36 to 0.77)	0.04
Global Assessment of Functioning
Main time effect	12.19	35	<.001	1.64 (1.37 to 1.92)	0.90
Time × treatment
ST vs TAU^c	2.68	745	.008	0.49 (0.13 to 0.84)	0.10
PGST vs TAU	1.09	704	.28	0.26 (–0.21 to 0.73)	0.04
IGST vs TAU^c	2.90	708	.004	0.67 (0.22 to 1.12)	0.11
IGST vs PGST	1.38	314	.17	0.41 (–0.17 to 0.99)	0.08
Social and Occupational Functioning Assessment Scale
Main time effect	10.36	31	<.001	1.51 (1.21 to 1.81)	0.88
Time × treatment
ST vs TAU^c	2.92	636	.004	0.48 (0.16 to 0.81)	0.12
PGST vs TAU	1.81	639	.07	0.40 (–0.04 to 0.84)	0.07
IGST vs TAU^c	2.56	624	.01	0.55 (0.13 to 0.97)	0.10
IGST vs PGST	0.52	389	.61	0.15 (–0.70 to 0.41)	0.03
Work and Social Adjustment Scale^e
Main time effect
Whole period	7.52	165	<.001	1.33 (0.81 to 1.86)	0.51
Years 2 and 3	−3.26	1120	.001	1.33 (0.81 to 1.86)	0.10
Time × treatment
ST vs TAU^c	2.88	990	.004	0.49 (0.16 to 0.82)	0.09
PGST vs TAU^c	2.32	1008	.02	0.52 (0.08 to 0.97)	0.07
IGST vs TAU^c	2.16	1003	.03	0.46 (0.04 to 0.88)	0.07
IGST vs PGST	−0.23	755	.82	−0.06 (–0.61 to 0.48)	0.01
World Health Organization Quality of Life assessment^f
Main time effect
Whole period	10.30	163	<.001	0.97 (0.68 to 1.26)	0.63
Years 2 and 3	−5.04	1119	<.001	0.97 (0.68 to 1.26)	0.15
Time × treatment
ST vs TAU^c	2.58	804	.01	0.26 (0.06 to 0.46)	0.09
PGST vs TAU	0.50	784	.62	0.07 (–0.20 to 0.33)	0.02
IGST vs TAU^c	3.37	787	<.001	0.43 (0.18 to 0.67)	0.12
IGST vs PGST^c	2.17	514	.03	0.36 (0.03 to 0.68)	0.10
Brief Symptom Inventory^e
Main time effect
Whole period	8.43	218	<.001	1.36 (0.94 to 1.78)	0.50
Years 2 and 3	−2.61	1140	.009	1.36 (0.94 to 1.78)	0.08
Time × treatment
ST vs TAU^c	2.81	888	.005	0.42 (0.13 to 0.72)	0.09
PGST vs TAU	1.48	848	.14	0.29 (–0.10 to 0.68)	0.05
IGST vs TAU^c	2.88	854	.004	0.54 (0.17 to 0.90)	0.10
IGST vs PGST	1.01	559	.31	0.24 (–0.23 to 0.71)	0.04
Young Schema Questionnaire–short form^f
Main time effect
Whole period	13.97	224	<.001	1.44 (1.11 to 1.79)	0.68
Years 2 and 3	−7.03	1014	<.001	1.44 (1.11 to 1.79)	0.22
Time × treatment
ST vs TAU^c	3.34	939	<.001	0.43 (0.18 to 0.68)	0.11
PGST vs TAU	1.82	809	.07	0.30 (–0.02 to 0.63)	0.06
IGST vs TAU^c	3.42	844	<.001	0.54 (0.23 to 0.85)	0.12
IGST vs PGST	1.18	405	.24	0.24 (–0.16 to 0.63)	0.06
Schema Mode Inventory–dysfunctional^f
Main time effect
Whole period	14.89	234	<.001	1.51 (1.17 to 1.86)	0.70
Years 2 and 3	−7.90	992	<.001	1.51 (1.17 to 1.86)	0.24
Time × treatment
ST vs TAU^c	2.44	997	.02	0.31 (0.06 to 1.86)	0.08
PGST vs TAU	1.24	842	.21	0.21 (–0.12 to 0.54)	0.04
IGST vs TAU^c	2.54	894	.01	0.41 (0.09 to 0.72)	0.08
IGST vs PGST	0.97	441	.33	0.20 (–0.20 to 0.59)	0.05
Schema Mode Inventory–functional^f
Main time effect
Whole period	12.09	217	<.001	1.19 (0.75 to 1.42)	0.63
Years 2 and 3	−6.66	1047	<.001	1.19 (0.75 to 1.42)	0.20
Time × treatment
ST vs TAU^c	2.58	805	.01	0.32 (0.08 to 0.57)	0.09
PGST vs TAU	0.89	743	.38	0.15 (–0.18 to 0.47)	0.03
IGST vs TAU^c	3.07	765	.002	0.48 (0.17 to 0.78)	0.11
IGST vs PGST	1.67	445	.10	0.33 (–0.06 to 0.72)	0.08
Happiness^f
Main time effect
Whole period	10.03	538	<.001	0.94 (0.59 to 1.29)	0.40
Years 2 and 3	−5.40	1384	<.001	0.94 (0.59 to 1.29)	0.14
Time × treatment
ST vs TAU^c	2.31	661	.02	0.29 (0.04 to 0.54)	0.09
PGST vs TAU^c	2.61	572	.009	0.42 (0.10 to 0.74)	0.11
IGST vs TAU	1.16	597	.25	0.18 (–0.12 to 0.48)	0.05
IGST vs PGST	1.30	264	.20	−0.18 (–0.48 to 0.12)	0.08
Working/studying proportion^g
Main time effect	1.40	33	.17	0.25 (–0.11 to 0.61)	0.24
Time × treatment
ST vs TAU^c	2.22	590	.03	0.59 (0.07 to 1.11)	0.09
PGST vs TAU	1.78	497	.08	0.60 (–0.06 to 1.27)	0.08
IGST vs TAU	1.84	477	.07	0.60 (–0.04 to 1.25)	0.08
IGST vs PGST	0.00	233	>.99	0.00 (–0.82 to 0.81)	0.00

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Abbreviations: GLMM, generalized linear mixed model; IGST, combination of individual and group schema therapy; PGST, predominantly group schema therapy; ST, schema therapy arms combined; TAU, (optimal) treatment as usual.

^{^a}

All analyses are based on GLMM with an autoregressive moving average (1,1) covariance structure for the repeated part and a random effect of time for a cohort within a site. Effect sizes d are based on the parameters of the GLMM analyses (change over time), with the square root of the baseline variance of a model with no random parts and only a fixed intercept as the denominator. Effect sizes r are defined as r = √(t²/[t² + df]). These represent the effect size associated with the effect tests in the fixed part of the GLMM. The t values and Cohen d values are positive when there is a positive effect (ie, a reduction over time, a larger reduction in ST than in TAU). The main time effect is the mean across ST and TAU.

^{^b}

Cohen d values are based on the parameters of the GLMM analyses (change over time), with the square root of the baseline variance of a model with no random parts and only a fixed intercept as the denominator (ie, SD baseline in transformed scale). The 95% CIs of the Cohen d are based on the 95% CIs of the slope differences from the GLMM.

^{^c}

The interaction of treatment by time was significant.

^{^d}

Analyzed with GLMM gamma regression with a log link. Estimated means are −46.99 points lower than on the original scale. Scores were transformed by subtracting 46.99 to bring the minimum to just greater than 0 to enable gamma regression.

^{^e}

Piecewise gamma regression with a general slope for time and an additional slope for the second and third year was used. Deleting the general time × treatment interaction from the model increased model fit; thus, the final model was time (general), time (years 2 and 3), treatment, and treatment × time (years 2 and 3). Interactions for the second time slope are shown (second and third year). To enable GLMM gamma regression with a log link, 0.1 was added to raw scores.

^{^f}

Piecewise regression with a general slope for time and an additional slope for the second and third year was used. Deleting the nonsignificant general time × treatment interaction from the model did not reduce model fit; thus, the final model was treatment, time (general), time (years 2 and 3), and time (years 2 and 3) × treatment. Interactions for the second time slope are shown (second and third year).

^{^g}

Analyzed with GLMM logistic regression. Estimated means are the proportion of working to studying.

When the 3 arms were mutually compared for treatment effectiveness, IGST was superior to PGST and TAU (IGST vs PGST: Cohen d, 0.84; 95% CI, 0.09-1.59; P = .03; IGST vs TAU: Cohen d, 1.14; 95% CI, 0.57-1.71; P < .001). The effectiveness of PGST did not differ significantly from that of TAU (Cohen d, 0.30; 95% CI, −0.29 to 0.89; P = .32) (Table 2, Table 3, and Figure 2A). The difference in effectiveness of IGST compared with TAU became significant at 1 year of treatment (difference, 2.59; 95% CI, 0.05-5.13; P = .048), and compared with PGST, at 2.5 years (difference, 2.68; 95% CI, 0.12-5.25; P = .04).

Figure 2. — A, Estimated marginal means and 95% CIs from the generalized linear mixed model (GLMM) analysis of the total BPDSI scores for the 3 treatment arms. The horizontal line indicates the clinical BPDSI cutoff score of 15, and whiskers indicate 95% CIs. B, Treatment retention by study arm quarterly for 2 years, from the GLMM survival analysis. IGST indicates combined individual and group schema therapy; PGST, predominantly group schema therapy; and TAU, (optimal) treatment as usual.

During the 3-year period, differences in slope between IGST and the other treatments attained large effect sizes (IGST vs TAU: Cohen d, 1.14; 95% CI, 0.57-1.71; P < .001; IGST vs PGST: Cohen d, 0.84; 95% CI, 0.09-1.59; P = .03) (Table 2 and Table 3). The TAU effect sizes at 1 year were 0.80 for the primary outcome and 0.56 for secondary non-BPDSI outcomes.

Results of a loc-f sensitivity analysis are given in eTable 3 in Supplement 2. Results of sensitivity analyses for different offset values are shown in eTable 4 in Supplement 2. Descriptive statistics of raw BPDSI scores and results in a transformed scale are shown in eTable 5 in Supplement 2.

Secondary Outcomes

Treatment Retention

Figure 2B shows treatment retention during years 1 and 2. The GLMM survival analysis on treatment dropout per yearly quarter showed no significant difference between ST and TAU but superiority of IGST compared with PGST (1 year: 0.82 vs 0.72; 2 years: 0.74 vs. 0.62) and TAU (1 year: 0.82 vs 0.73; 2 years: 0.74 vs 0.64). Treatment as usual and PGST did not differ significantly for treatment retention (1 year: 0.73 vs 0.72; 2 years: 0.64 vs 0.62) (eTable 5 in Supplement 2).

Severity per BPD Trait

Predominantly group ST and IGST combined were superior to TAU on 6 of the 9 BPDSI subscales (binomial test, P < .001) (eTable 6 in Supplement 2); IGST was superior to TAU on 7 subscales (binomial test, P < .001) and to PGST on 2 subscales (binomial test, P = .07). PGST was not significantly different from TAU on any of the subscales (binomial test, P > .99). The effects of PGST were between those of TAU and IGST for all subscales apart from emptiness, for which the effect of PGST was smaller than that of TAU.

Suicidality and Suicide Attempts

For scores on suicidality items of the BPDSI (para)suicide scale, PGST and IGST combined were superior to TAU (eTable 6 in Supplement 2). Only IGST was superior to TAU; IGST and PGST did not differ significantly in reducing suicidality scores.

Overall, the number of suicide attempts during the previous 3 months reduced with time, with a nonsignificant difference between ST and TAU but with IGST being significantly superior to TAU in reducing suicide attempts (eTable 6 in Supplement 2).

Secondary Outcomes Not Based on BPDSI

For all 11 secondary outcomes, PGST and IGST combined were superior to TAU (binomial test, P < .001); IGST was superior to TAU for 9 of the 11 outcomes (binomial test, P < .001) (Table 2 and Table 3). PGST was superior to TAU for only 2 outcomes (the Work and Social Adjustment Scale and happiness; binomial test, P = .10). IGST was superior to PGST for 1 of 11 secondary outcomes (binomial test, P = .43), the World Health Organization Quality of Life Assessment. The overall ST effect was largely attributable to IGST, with PGST outcomes between those of TAU and IGST.

During the study period, 3 patients died of suicide (1 from each treatment arm). The patient from the PGST arm applied successfully to a euthanasia clinic during the first 3 months (quarter 1) of treatment. The patient from the IGST arm died by suicide approximately 8 months after discontinuing treatment and study during quarter 2 (months 4 to 6). A TAU recipient died by suicide during quarter 3 (months 7 to 9). In the TAU arm, an additional patient died in quarter 2 of an unknown cause; suicide was suspected but not confirmed.

Deterioration

Deterioration was defined as a BPDSI score increase of 11.70 or greater compared with baseline.³ Of the available BPDSI assessments, more deteriorations were observed in the TAU arm (16 of 745 assessments [2.1%]) than in the PGST arm (5 of 398 [1.25%]) and the IGST arm (4 of 452 [0.88%]).

Discussion

This international RCT compared 2 ST formats (PGST and IGST) with TAU and with each other in the treatment of BPD across 15 sites in 5 countries. Although the PGST and IGST combined appeared to be superior to TAU in reducing BPD severity (the primary outcome) and for most secondary outcomes, most effects were attributable to IGST; there were also fewer suicide attempts and treatment dropouts in this arm. IGST was superior to TAU in reducing BPD severity and for 7 BPDSI subscales. Moreover, IGST was superior to PGST in reducing BPD severity and for 2 BPDSI subscales. In summary, the results support IGST as an effective, acceptable (as indexed by treatment retention), and safe treatment for BPD, whereas the results were more equivocal for PGST.

The 3-year effects were generally large in all arms. Treatment as usual was effective given the within-condition effect sizes. Compared with the pooled pretreatment-posttreatment effect size of 0.5 for dialectical behavior therapy,²² usually found at 1 year, the TAU effect sizes at 1 year in our study were similar (0.80 for the primary outcome and a mean effect size of 0.56 for secondary non-BPDSI outcomes). This indicates that optimal TAU was offered.

With regard to the reason that IGST was superior to PGST, IGST had relatively large effects on schemas, schema modes, and affective instability, variables that are assumed to underlie change processes.^23,24 Core emotional needs such as safe attachment and positive attention are often not adequately met during childhood in patients with BPD in both individual and group relationships. The combined ST format aimed to meet needs in both contexts, whereas PGST provided less individual attention. Moreover, addressing severe problems and childhood trauma might be easier for therapists in individual treatment than in group treatment. This was reported by participating therapists in a qualitative ancillary study.²⁵ Consistent with these hypotheses, patients in another ancillary qualitative study²⁶ stated that individual ST was important to discuss sensitive topics on a deeper, more personal level. Most patients (75%) emphasized the importance of individual ST in conjunction with group ST, and 70% of the participants in receiving PGST expressed the need for more individual sessions. Also indicative of the importance of individual ST, PGST participants in the current study generally used the maximum number of individual sessions. How well individual ST compares with IGST and which format is optimal for whom are topics for future studies.

When comparing, to our knowledge, the first RCT on individual ST for BPD³ with the present study, there appeared to be equivalent effect sizes. There were more sessions in the former study (approximately double), but the dropout rate was lower. Group treatment might be associated with increased dropout for a variety of reasons, including distrust, frightening group processes, or lack of an individualized agenda. Some patients in the ancillary qualitative study²⁶ described hostility from group members as particularly difficult. Individual sessions might mitigate the problem of aversive group dynamics.

The present study has some implications about the sufficient dosage of ST sessions. A finding of note was the continuation of symptom improvement during years 2 and 3. In the ST arms, session frequency was reduced to only once a month using a tapered schedule, and in year 3, no further treatment was offered. Although patients often resist this tapering, feeling not ready and expressing fear of relapse,²⁶ in our study, they tended to do well. At the 3-year follow-up, some participants expressed how helpful it was to discover that they were able to apply what they learned after therapy was discontinued. They commented that this helped to increase their self-confidence and changed their self-view as a patient with chronic mental illness who is dependent on long-term mental health care.

Despite the generally positive results, there were 3 suicides and 1 death of unknown cause during the study, with 1 suicide in each treatment arm. One of the deaths was related to a preset plan to apply for euthanasia that the person did not share with the treating team. Another participant died by suicide after dropping out of treatment. Nevertheless, in general, suicidality was reduced during treatment, as were suicide attempts, with IGST being superior to TAU in reducing suicidality and suicide attempts.

Limitations

This study had several limitations. First, the worldwide financial crisis of 2007-2008, followed by an economic crisis (in most countries), interfered with study implementation, leading some sites that had planned to participate to withdraw owing to cutbacks. This had to be compensated by recruiting additional sites and by sites including additional cohorts. Although the mean rank order of the ST formats was equal, the distribution deviated from the original plan. Second, as with all RCTs, participants dropped out of the study, which can affect the validity of the results. Third, rating of TAU recordings to assess differentiation between ST and TAU was impossible. However, patients’ self-reports supported that ST was different from TAU. Moreover, assessments of adherence to ST by independent raters supported that ST was generally delivered at a good level of quality. Fourth, group ST was generally delivered by novice group ST therapists who were specifically trained for the study without having had the opportunity to learn the intervention before the study commenced. Some aspects of the group intervention (eg, early conflict management) required a high skill level. For some of the individual ST therapists, it was the first time they applied ST. Thus, ST effects might increase and the number of dropouts may be reduced with experience, repeated training, and supervision. Fifth, TAU was unstandardized. Future RCTs should compare ST with other specialized psychotherapies, controlling for intensity of treatment.

Conclusions

In this RCT, IGST was more effective in reducing the severity of BPD compared with TAU and PGST. However, PGST was not more effective than TAU. The international multicenter design, the size of the study population, and the execution of the study in regular mental health services that were treating BPD support the generalizability of the results. However, this study did not compare ST with another specialized psychotherapy, and no conclusions in this respect can be made. The cost-effectiveness of ST is a subject for further study. Future research should focus on the direct comparison of individual and combined ST formats; the testing of less extreme combinations of group and individual ST; direct comparisons of ST with other evidence-based treatments, including the study of factors associated with better treatment allocation; and the testing of ST in countries in other regions of the world.

Supplement 1.

Trial Protocol

Click here for additional data file.^{(282.3KB, pdf)}

Supplement 2.

eAppendix 1. Overview of Sites and Cohorts per Site

eAppendix 2. Deviations From the Original Plan

eTable 1. Overview of Type and Frequency of Sessions Over 2 Years for PGST and IGST

eTable 2. Overview of Initial TAU per Site

eAppendix 3. Assessment of Treatment Integrity

eAppendix 4. Clinical Outcome Measures

eAppendix 5. Overview of Random Effects for Secondary Outcomes

eAppendix 6. Estimation Procedures for the Effect Size Cohen d and its 95% CI

eTable 3. Results of Loc-f Sensitivity Analysis

eTable 4. Sensitivity Analysis of the Zero-Offset Value for the Gamma Regression of the BPDSI Total Score

eTable 5. Descriptive Statistics of Observed BPDSI Total Scores, GLMM Results in Transformed Scale, Pairwise Contrasts at 3 years in Original Scale, Treatment Retention per 3 Months by Treatment Arm

eTable 6. BPDSI-Based Secondary Outcomes: BSPDI Subscales, Suicidality, Suicide Attempts

Click here for additional data file.^{(608.9KB, pdf)}

Supplement 3.

Data Sharing Statement

Click here for additional data file.^{(20.5KB, pdf)}

References

1.Storebø OJ, Stoffers-Winterling JM, Völlm BA, et al. Psychological therapies for people with borderline personality disorder. Cochrane Database Syst Rev. 2020;5:CD012955. [DOI] [PMC free article] [PubMed] [Google Scholar]
2.Oud M, Arntz A, Hermens ML, Verhoef R, Kendall T. Specialized psychotherapies for adults with borderline personality disorder: a systematic review and meta-analysis. Aust N Z J Psychiatry. 2018;52(10):949-961. doi: 10.1177/0004867418791257 [DOI] [PMC free article] [PubMed] [Google Scholar]
3.Giesen-Bloo J, van Dyck R, Spinhoven P, et al. Outpatient psychotherapy for borderline personality disorder: randomized trial of schema-focused therapy vs transference-focused psychotherapy. Arch Gen Psychiatry. 2006;63(6):649-658. doi: 10.1001/archpsyc.63.6.649 [DOI] [PubMed] [Google Scholar]
4.Nadort M, Arntz A, Smit JH, et al. Implementation of outpatient schema therapy for borderline personality disorder with versus without crisis support by the therapist outside office hours: a randomized trial. Behav Res Ther. 2009;47(11):961-973. doi: 10.1016/j.brat.2009.07.013 [DOI] [PubMed] [Google Scholar]
5.Farrell JM, Shaw IA, Webber MA. A schema-focused approach to group psychotherapy for outpatients with borderline personality disorder: a randomized controlled trial. J Behav Ther Exp Psychiatry. 2009;40(2):317-328. doi: 10.1016/j.jbtep.2009.01.002 [DOI] [PubMed] [Google Scholar]
6.Weertman A, Arntz A. Effectiveness of treatment of childhood memories in cognitive therapy for personality disorders: a controlled study contrasting methods focusing on the present and methods focusing on childhood memories. Behav Res Ther. 2007;45(9):2133-2143. doi: 10.1016/j.brat.2007.02.013 [DOI] [PubMed] [Google Scholar]
7.Arntz A, van Genderen H.. Schema Therapy for Borderline Personality Disorder. Wiley Blackwell; 2009. [Google Scholar]
8.Wetzelaer P, Farrell J, Evers SMMA, et al. Design of an international multicentre RCT on group schema therapy for borderline personality disorder. BMC Psychiatry. 2014;14:319. doi: 10.1186/s12888-014-0319-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
9.Farrell JM, Shaw IA. Group Schema Therapy for Borderline Personality Disorder: A Step-by-Step Treatment Manual With Patient Workbook. John Wiley & Sons; 2012. doi: 10.1002/9781119943167 [DOI] [Google Scholar]
10.Farrell JM, Reiss N, Shaw IA. The Schema Therapy Clinician’s Guide: A Complete Resource for Building and Delivering Individual, Group and Integrated Schema Mode Treatment Programs. John Wiley & Sons; 2014. doi: 10.1002/9781118510018 [DOI] [Google Scholar]
11.Bastick E, Bot S, Verhagen SJW, et al. The development and psychometric evaluation of the Group Schema Therapy Rating Scale–Revised. Behav Cogn Psychother. 2018;46(5):601-618. doi: 10.1017/S1352465817000741 [DOI] [PubMed] [Google Scholar]
12.Arntz A, van den Hoorn M, Cornelis J, Verheul R, van den Bosch WM, de Bie AJHT. Reliability and validity of the borderline personality disorder severity index. J Pers Disord. 2003;17(1):45-59. doi: 10.1521/pedi.17.1.45.24053 [DOI] [PubMed] [Google Scholar]
13.Bloo J, Arntz A, Schouten E.. The Borderline Personality Disorder Checklist: psychometric evaluation and factorial structure in clinical and nonclinical samples. Ann Psychol. 2017; 20(2): 281-336. doi: 10.18290/rpsych.2017.20.2-3en [DOI] [Google Scholar]
14.Goldman HH, Skodol AE, Lave TR. Revising Axis V for DSM-IV: a review of measures of social functioning. Am J Psychiatry. 1992;149(9):1148-1156. doi: 10.1176/ajp.149.9.1148 [DOI] [PubMed] [Google Scholar]
15.Derogatis LR, Melisaratos N. The Brief Symptom Inventory: an introductory report. Psychol Med. 1983;13(3):595-605. doi: 10.1017/S0033291700048017 [DOI] [PubMed] [Google Scholar]
16.Mundt JC, Marks IM, Shear MK, Greist JH. The Work and Social Adjustment Scale: a simple measure of impairment in functioning. Br J Psychiatry. 2002;180:461-464. doi: 10.1192/bjp.180.5.461 [DOI] [PubMed] [Google Scholar]
17.The WHOQOL Group . Development of the World Health Organization WHOQOL-BREF quality of life assessment. Psychol Med. 1998;28(3):551-558. doi: 10.1017/S0033291798006667 [DOI] [PubMed] [Google Scholar]
18.Young JE, Brown G. Young Schema Questionnaire Short Form. Cognitive Therapy Center; 1998. [Google Scholar]
19.Lobbestael J, van Vreeswijk M, Spinhoven P, Schouten E, Arntz A. Reliability and validity of the short Schema Mode Inventory (SMI). Behav Cogn Psychother. 2010;38(4):437-458. doi: 10.1017/S1352465810000226 [DOI] [PubMed] [Google Scholar]
20.Bamelis LL, Evers SM, Spinhoven P, Arntz A. Results of a multicenter randomized controlled trial of the clinical effectiveness of schema therapy for personality disorders. Am J Psychiatry. 2014;171(3):305-322. doi: 10.1176/appi.ajp.2013.12040518 [DOI] [PubMed] [Google Scholar]
21.Wilkinson B. A statistical consideration in psychological research. Psychol Bull. 1951;48(3):156-158. doi: 10.1037/h0059111 [DOI] [PubMed] [Google Scholar]
22.Kliem S, Kröger C, Kosfelder J. Dialectical behavior therapy for borderline personality disorder: a meta-analysis using mixed-effects modeling. J Consult Clin Psychol. 2010;78(6):936-951. doi: 10.1037/a0021015 [DOI] [PubMed] [Google Scholar]
23.Yakın D, Grasman R, Arntz A. Schema modes as a common mechanism of change in personality pathology and functioning: results from a randomized controlled trial. Behav Res Ther. 2020;126:103553. doi: 10.1016/j.brat.2020.103553 [DOI] [PubMed] [Google Scholar]
24.Von Klipstein L, Borsboom D, Arntz A. The exploratory value of cross-sectional partial correlation networks: predicting relationships between change trajectories in borderline personality disorder. PloS One. 2021;16(7):e0254496. doi: 10.1371/journal.pone.0254496 [DOI] [PMC free article] [PubMed] [Google Scholar]
25.Martius D. The experience of schema therapists who provided the treatment: what we learnt. Paper presented at: 9th World Congress of Behavioural and Cognitive Therapies; July 17-20, 2019; Berlin. Accessed January 28, 2022. https://wcbct2019.org/Downloads/Congress-Programme.pdf/ [Google Scholar]
26.Tan YM, Lee CW, Averbeck LE, et al. Schema therapy for borderline personality disorder: a qualitative study of patients’ perceptions. PloS One. 2018;13(11):e0206039. doi: 10.1371/journal.pone.0206039 [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

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

Supplementary Materials

Supplement 1.

Trial Protocol

Click here for additional data file.^{(282.3KB, pdf)}

Supplement 2.

eAppendix 1. Overview of Sites and Cohorts per Site

eAppendix 2. Deviations From the Original Plan

eTable 1. Overview of Type and Frequency of Sessions Over 2 Years for PGST and IGST

eTable 2. Overview of Initial TAU per Site

eAppendix 3. Assessment of Treatment Integrity

eAppendix 4. Clinical Outcome Measures

eAppendix 5. Overview of Random Effects for Secondary Outcomes

eAppendix 6. Estimation Procedures for the Effect Size Cohen d and its 95% CI

eTable 3. Results of Loc-f Sensitivity Analysis

eTable 4. Sensitivity Analysis of the Zero-Offset Value for the Gamma Regression of the BPDSI Total Score

eTable 6. BPDSI-Based Secondary Outcomes: BSPDI Subscales, Suicidality, Suicide Attempts

Click here for additional data file.^{(608.9KB, pdf)}

Supplement 3.

Data Sharing Statement

Click here for additional data file.^{(20.5KB, pdf)}

[yoi220001r1] 1.Storebø OJ, Stoffers-Winterling JM, Völlm BA, et al. Psychological therapies for people with borderline personality disorder. Cochrane Database Syst Rev. 2020;5:CD012955. [DOI] [PMC free article] [PubMed] [Google Scholar]

[yoi220001r2] 2.Oud M, Arntz A, Hermens ML, Verhoef R, Kendall T. Specialized psychotherapies for adults with borderline personality disorder: a systematic review and meta-analysis. Aust N Z J Psychiatry. 2018;52(10):949-961. doi: 10.1177/0004867418791257 [DOI] [PMC free article] [PubMed] [Google Scholar]

[yoi220001r3] 3.Giesen-Bloo J, van Dyck R, Spinhoven P, et al. Outpatient psychotherapy for borderline personality disorder: randomized trial of schema-focused therapy vs transference-focused psychotherapy. Arch Gen Psychiatry. 2006;63(6):649-658. doi: 10.1001/archpsyc.63.6.649 [DOI] [PubMed] [Google Scholar]

[yoi220001r4] 4.Nadort M, Arntz A, Smit JH, et al. Implementation of outpatient schema therapy for borderline personality disorder with versus without crisis support by the therapist outside office hours: a randomized trial. Behav Res Ther. 2009;47(11):961-973. doi: 10.1016/j.brat.2009.07.013 [DOI] [PubMed] [Google Scholar]

[yoi220001r5] 5.Farrell JM, Shaw IA, Webber MA. A schema-focused approach to group psychotherapy for outpatients with borderline personality disorder: a randomized controlled trial. J Behav Ther Exp Psychiatry. 2009;40(2):317-328. doi: 10.1016/j.jbtep.2009.01.002 [DOI] [PubMed] [Google Scholar]

[yoi220001r6] 6.Weertman A, Arntz A. Effectiveness of treatment of childhood memories in cognitive therapy for personality disorders: a controlled study contrasting methods focusing on the present and methods focusing on childhood memories. Behav Res Ther. 2007;45(9):2133-2143. doi: 10.1016/j.brat.2007.02.013 [DOI] [PubMed] [Google Scholar]

[yoi220001r7] 7.Arntz A, van Genderen H.. Schema Therapy for Borderline Personality Disorder. Wiley Blackwell; 2009. [Google Scholar]

[yoi220001r8] 8.Wetzelaer P, Farrell J, Evers SMMA, et al. Design of an international multicentre RCT on group schema therapy for borderline personality disorder. BMC Psychiatry. 2014;14:319. doi: 10.1186/s12888-014-0319-3 [DOI] [PMC free article] [PubMed] [Google Scholar]

[yoi220001r9] 9.Farrell JM, Shaw IA. Group Schema Therapy for Borderline Personality Disorder: A Step-by-Step Treatment Manual With Patient Workbook. John Wiley & Sons; 2012. doi: 10.1002/9781119943167 [DOI] [Google Scholar]

[yoi220001r10] 10.Farrell JM, Reiss N, Shaw IA. The Schema Therapy Clinician’s Guide: A Complete Resource for Building and Delivering Individual, Group and Integrated Schema Mode Treatment Programs. John Wiley & Sons; 2014. doi: 10.1002/9781118510018 [DOI] [Google Scholar]

[yoi220001r11] 11.Bastick E, Bot S, Verhagen SJW, et al. The development and psychometric evaluation of the Group Schema Therapy Rating Scale–Revised. Behav Cogn Psychother. 2018;46(5):601-618. doi: 10.1017/S1352465817000741 [DOI] [PubMed] [Google Scholar]

[yoi220001r12] 12.Arntz A, van den Hoorn M, Cornelis J, Verheul R, van den Bosch WM, de Bie AJHT. Reliability and validity of the borderline personality disorder severity index. J Pers Disord. 2003;17(1):45-59. doi: 10.1521/pedi.17.1.45.24053 [DOI] [PubMed] [Google Scholar]

[yoi220001r13] 13.Bloo J, Arntz A, Schouten E.. The Borderline Personality Disorder Checklist: psychometric evaluation and factorial structure in clinical and nonclinical samples. Ann Psychol. 2017; 20(2): 281-336. doi: 10.18290/rpsych.2017.20.2-3en [DOI] [Google Scholar]

[yoi220001r14] 14.Goldman HH, Skodol AE, Lave TR. Revising Axis V for DSM-IV: a review of measures of social functioning. Am J Psychiatry. 1992;149(9):1148-1156. doi: 10.1176/ajp.149.9.1148 [DOI] [PubMed] [Google Scholar]

[yoi220001r15] 15.Derogatis LR, Melisaratos N. The Brief Symptom Inventory: an introductory report. Psychol Med. 1983;13(3):595-605. doi: 10.1017/S0033291700048017 [DOI] [PubMed] [Google Scholar]

[yoi220001r16] 16.Mundt JC, Marks IM, Shear MK, Greist JH. The Work and Social Adjustment Scale: a simple measure of impairment in functioning. Br J Psychiatry. 2002;180:461-464. doi: 10.1192/bjp.180.5.461 [DOI] [PubMed] [Google Scholar]

[yoi220001r17] 17.The WHOQOL Group . Development of the World Health Organization WHOQOL-BREF quality of life assessment. Psychol Med. 1998;28(3):551-558. doi: 10.1017/S0033291798006667 [DOI] [PubMed] [Google Scholar]

[yoi220001r18] 18.Young JE, Brown G. Young Schema Questionnaire Short Form. Cognitive Therapy Center; 1998. [Google Scholar]

[yoi220001r19] 19.Lobbestael J, van Vreeswijk M, Spinhoven P, Schouten E, Arntz A. Reliability and validity of the short Schema Mode Inventory (SMI). Behav Cogn Psychother. 2010;38(4):437-458. doi: 10.1017/S1352465810000226 [DOI] [PubMed] [Google Scholar]

[yoi220001r20] 20.Bamelis LL, Evers SM, Spinhoven P, Arntz A. Results of a multicenter randomized controlled trial of the clinical effectiveness of schema therapy for personality disorders. Am J Psychiatry. 2014;171(3):305-322. doi: 10.1176/appi.ajp.2013.12040518 [DOI] [PubMed] [Google Scholar]

[yoi220001r21] 21.Wilkinson B. A statistical consideration in psychological research. Psychol Bull. 1951;48(3):156-158. doi: 10.1037/h0059111 [DOI] [PubMed] [Google Scholar]

[yoi220001r22] 22.Kliem S, Kröger C, Kosfelder J. Dialectical behavior therapy for borderline personality disorder: a meta-analysis using mixed-effects modeling. J Consult Clin Psychol. 2010;78(6):936-951. doi: 10.1037/a0021015 [DOI] [PubMed] [Google Scholar]

[yoi220001r23] 23.Yakın D, Grasman R, Arntz A. Schema modes as a common mechanism of change in personality pathology and functioning: results from a randomized controlled trial. Behav Res Ther. 2020;126:103553. doi: 10.1016/j.brat.2020.103553 [DOI] [PubMed] [Google Scholar]

[yoi220001r24] 24.Von Klipstein L, Borsboom D, Arntz A. The exploratory value of cross-sectional partial correlation networks: predicting relationships between change trajectories in borderline personality disorder. PloS One. 2021;16(7):e0254496. doi: 10.1371/journal.pone.0254496 [DOI] [PMC free article] [PubMed] [Google Scholar]

[yoi220001r25] 25.Martius D. The experience of schema therapists who provided the treatment: what we learnt. Paper presented at: 9th World Congress of Behavioural and Cognitive Therapies; July 17-20, 2019; Berlin. Accessed January 28, 2022. https://wcbct2019.org/Downloads/Congress-Programme.pdf/ [Google Scholar]

[yoi220001r26] 26.Tan YM, Lee CW, Averbeck LE, et al. Schema therapy for borderline personality disorder: a qualitative study of patients’ perceptions. PloS One. 2018;13(11):e0206039. doi: 10.1371/journal.pone.0206039 [DOI] [PMC free article] [PubMed] [Google Scholar]

PERMALINK

Effectiveness of Predominantly Group Schema Therapy and Combined Individual and Group Schema Therapy for Borderline Personality Disorder

Arnoud Arntz, PhD

Gitta A Jacob, PhD

Christopher W Lee, PhD

Odette Manon Brand-de Wilde, PhD

Eva Fassbinder, MD

R Patrick Harper, MSc

Anna Lavender, DClinPsy

George Lockwood, PhD

Ioannis A Malogiannis, DrMed

Florian A Ruths, DrMed

Ulrich Schweiger, DrMed

Ida A Shaw, MA

Gerhard Zarbock, PhD

Joan M Farrell, PhD

Key Points

Question

Findings

Meaning

Abstract

Importance

Objective

Design, Setting, and Participants

Interventions

Main Outcomes and Measures

Results

Conclusions and Relevance

Trial Registration

Introduction

Methods

Study Design

Patients

Figure 1. CONSORT Diagram.

Randomization and Masking

Procedures

Treatments and Therapists

Treatment Integrity and Assessments

Outcomes

Statistical Analysis

Results

Table 1. Descriptive Statistics at Baseline and Treatment Integrity Test Results.

Assessment of Treatment Integrity

Primary Outcomes

Table 2. Estimated Means, 95% CIs, and Effect Sizes for the Primary and Secondary Outcomes.

Table 3. Comparison of Time Effects for First and Secondary Outcomes Between the ST Groups Combined vs the TAU Group, the PGST Group vs the TAU Group, the IGST Group vs the TAU Group, and the IGST Group vs the PGST Groupa.

Figure 2. Borderline Personality Disorder Severity Index (BPDSI) Scores and Duration of Treatment Retention.

Secondary Outcomes

Treatment Retention

Severity per BPD Trait

Suicidality and Suicide Attempts

Secondary Outcomes Not Based on BPDSI

Deterioration

Discussion

Limitations

Conclusions

References

Associated Data

Supplementary Materials

ACTIONS

PERMALINK

RESOURCES

Similar articles

Cited by other articles

Links to NCBI Databases

Table 3. Comparison of Time Effects for First and Secondary Outcomes Between the ST Groups Combined vs the TAU Group, the PGST Group vs the TAU Group, the IGST Group vs the TAU Group, and the IGST Group vs the PGST Group^a.