Evidence map›Paper›PMID 40753432›Full record

ArticleTrials2025

A mechanism-based group psychotherapy approach to aggressive behavior (MAAP) in borderline personality disorder: a multicenter randomized controlled clinical trial.

Christine Sigrist, Andreas Bechdolf, Katja Bertsch, Robin Bullenkamp, Martin Busse, Ute Gr Darrelmann, Astrid Dempfle, Martin Driessen, Thomas Frodl, Jan-Michael Kersting and 15 more

Abstract readClinical Trial Protocol
In one paragraph

Article in Trials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors.

Christine SigristDepartment of General Psychiatry, Heidelberg University, Heidelberg, Germany. christine.sigrist@med.uni-heidelberg.de.ORCID http://orcid.org/0000-0002-6718-3230
Andreas BechdolfDepartment of Psychiatry, Psychotherapy and Psychosomatics, Vivantes Klinikum Am Urban and Vivantes Klinikum Im Friedrichshain, Berlin, Germany.
Katja BertschDepartment of Psychology, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.
Robin BullenkampDepartment of General Psychiatry, Heidelberg University, Heidelberg, Germany.
Martin BusseDepartment of General Psychiatry, Heidelberg University, Heidelberg, Germany.
Ute Gr DarrelmannDepartment of Psychiatry and Psychotherapy, University Hospital Bonn, Bonn, Germany.
Astrid DempfleInstitute of Medical Informatics and Statistics, Christian-Albrechts University of Kiel, Kiel, Germany.
Martin DriessenDepartment of Psychiatry and Psychotherapy, Evangelisches Klinikum Bethel, Bielefeld, Germany.
Thomas FrodlDepartment of Psychiatry and Psychotherapy, University Hospital Aachen, RWTH, Aachen, Germany.
Jan-Michael KerstingDepartment of General Psychiatry, Heidelberg University, Heidelberg, Germany.
Jessica KesikDepartment of Psychiatry and Psychotherapy, University Hospital Aachen, RWTH, Aachen, Germany.
Burkhart MatzkeDepartment of General Psychiatry, Heidelberg University, Heidelberg, Germany.
Corinne NeukelDepartment of General Psychiatry, Heidelberg University, Heidelberg, Germany.
Eva NiessenDepartment of Psychiatry and Psychotherapy, Evangelisches Klinikum Bethel, Bielefeld, Germany.
Svenja NückelDepartment of Psychiatry and Psychotherapy, University Hospital LMU, Munich, Germany.
Viola OertelDepartment of Psychiatry, Psychosomatic Medicine and Psychotherapy, University Hospital Frankfurt, Frankfurt Am Main, Germany.
Frank PadbergDepartment of Psychiatry and Psychotherapy, University Hospital LMU, Munich, Germany.
Alexandra PhilipsenDepartment of Psychiatry and Psychotherapy, University Hospital Bonn, Bonn, Germany.
Dorothee PinkDepartment of Psychiatry, Psychotherapy and Psychosomatics, Vivantes Klinikum Am Urban and Vivantes Klinikum Im Friedrichshain, Berlin, Germany.
Andreas ReifDepartment of Psychiatry, Psychosomatic Medicine and Psychotherapy, University Hospital Frankfurt, Frankfurt Am Main, Germany.
Matthias ReinhardDepartment of Psychiatry and Psychotherapy, University Hospital LMU, Munich, Germany.
Carolin SteuweDepartment of Psychiatry and Psychotherapy, Evangelisches Klinikum Bethel, Bielefeld, Germany.
Larissa WolkensteinDepartment of Psychology, LMU, Munich, Germany.
Sabine C HerpertzDepartment of General Psychiatry, Heidelberg University, Heidelberg, Germany.
The Maap Consortium

Funding

Deutsche Forschungsgemeinschaft 462340798
6 · The paper itself

Abstract

backgroundHigh levels of trait anger and aggressive behavior are common and problematic phenomena in patients with borderline personality disorder (BPD). In BPD, patterns of reactive aggression often lead to functional impairment affecting important areas of life. Despite the high burden on individuals and their social environment, there are no specific, cost-effective treatments to reduce aggression in BPD. In previous studies, we and others have been able to infer specific biobehavioral mechanisms underlying patterns of reactive aggression in BPD that can be used as potential treatment targets. To address this, we developed a mechanism-based anti-aggression psychotherapy (MAAP) for the group setting that specifically targets the biobehavioral mechanisms underlying outward-directed aggression in BPD. A previously conducted proof-of-concept study had suggested beneficial effects for this neglected group of patients.

methodsIn this multicenter, confirmatory, randomized-controlled-clinical-trial, MAAP, which consists of multifaceted, evidence-based treatment elements adapted from other sophisticated treatment programs such as Dialectical Behavior Therapy and Mentalization-Based Treatment, is tested for efficacy against a non-specific supportive psychotherapy (NSSP) program focusing on non-specific general factors of psychotherapy at seven different sites in Germany. Both treatment arms, based on one individual and 13 group therapeutic sessions (1.5 h per session, twice a week), are delivered over a period of 7-10 weeks. A total of N = 186 patients will be recruited, half of whom will be cluster-randomized to MAAP. Outcomes are assessed at baseline, immediately, and 4, 12, 20, and 24 weeks post-treatment using ecological momentary assessment, clinical interviews, questionnaires, and online tasks. DISCUSSION: If proven superior, MAAP can be incorporated into standard psychiatric care, filling a critical gap in the current therapeutic landscape by offering a structured, cost-effective, and evidence-based treatment that directly targets the biobehavioral mechanisms underlying reactive aggression in BPD. By potentially improving clinical outcomes and reducing the burden of reactive aggression in BPD, MAAP could be beneficial for both individuals and their social environments. The study's large, multicenter design enhances the generalizability of the results, making them more relevant for broader clinical applications.

trial registrationThis study was registered in the German Clinical Trials Register DRKS (DRKS00031608) on 31.10.2023 ( https://drks.de/search/de/trial/DRKS00031608 ).

Indexed as

AggressionBorderline Personality DisorderPsychotherapy, GroupAdultFemaleGermanyHumansMaleMulticenter Studies as TopicRandomized Controlled Trials as TopicTime FactorsTreatment OutcomeYoung AdultAggressive behaviorAngerBorderline personality disorderDialectic behavior therapyEmotion regulationGroup psychotherapyImpulsivityMentalization-based therapyMindfulnessReactive aggression

Identifiers

PMID40753432
PMCPMC12317525

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.