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Efficacy and cost-effectiveness of a Transdiagnostic group-based exercise intervention: study protocol for a pragmatic multi-site randomized controlled trial

  • Sebastian Wolf*
  • , Britta Seiffer
  • , Johanna Marie Zeibig
  • , Jana Welkerling
  • , Leonie Louisa Bauer
  • , Anna Katharina Frei
  • , Thomas Studnitz
  • , Stephanie Rosenstiel
  • , David Victor Fiedler
  • , Florian Helmhold
  • , Andreas Ray
  • , Eva Herzog
  • , Keisuke Takano
  • , Tristan Nakagawa
  • , Saskia Kropp
  • , Sebastian Franke
  • , Stefan Peters
  • , Nadja El-Kurd
  • , Lena Zwanzleitner
  • , Leonie Sundmacher
  • Ander Ramos-Murguialday, Martin Hautzinger, Gorden Sudeck, Thomas Ehring
*Autor correspondiente de este trabajo

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

11 Citas (Scopus)

Resumen

Background: Mental disorders are prevalent and cause considerable burden of disease. Exercise has been shown to be efficacious to treat major depressive disorders, insomnia, panic disorder with and without agoraphobia and post traumatic stress disorder (PTSD). Methods: This pragmatic, two arm, multi-site randomised controlled trial will evaluate the efficacy and cost-effectiveness of the manualized, group-based six-months exercise intervention “ImPuls”, among physically inactive patients with major depressive disorders, insomnia, panic disorder, agoraphobia and PTSD within a naturalistic outpatient context in Germany. A minimum of 375 eligible outpatients from 10 different study sites will be block-randomized to either ImPuls in addition to treatment as usual (TAU) or TAU only. ImPuls will be conducted by trained exercise therapists and delivered in groups of six patients. The program will combine (a) moderate to vigorous aerobic exercise carried out two-three times a week for at least 30 min with (b) behavior change techniques for sustained exercise behavior change. All outcomes will be assessed pre-treatment, post-treatment (six months after randomization) and at follow-up (12 months after randomization). Primary outcome will be self-reported global symptom severity assessed with the Brief Symptom Inventory (BSI-18). Secondary outcomes will be accelerometry-based moderate to vigorous physical activity, self-reported exercise, disorder-specific symptoms, quality-adjusted life years (QALY) and healthcare costs. Intention-to-treat analyses will be conducted using mixed models. Cost-effectiveness and cost-utility analysis will be conducted using incremental cost-effectiveness and cost-utility ratios. Discussion: Despite its promising therapeutic effects, exercise programs are currently not provided within the outpatient mental health care system in Germany. This trial will inform service providers and policy makers about the efficacy and cost-effectiveness of the group-based exercise intervention ImPuls within a naturalistic outpatient health care setting. Group-based exercise interventions might provide an option to close the treatment gap within outpatient mental health care settings. Trial registration: The study was registered in the German Clinical Trials Register (ID: DRKS00024152, 05/02/2021).

Idioma originalInglés
Número de artículo540
PublicaciónBMC Psychiatry
Volumen21
N.º1
DOI
EstadoPublicada - dic 2021
Publicado de forma externa

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