| Autor: |
Stefan M Gold, ProfPhD, Tim Friede, ProfPhD, Björn Meyer, PhD, Rona Moss-Morris, ProfPhD, Joanna Hudson, PhD, Susanna Asseyer, MD, Judith Bellmann-Strobl, MD, Andreas Leisdon, MSc, Leonie Ißels, MSc, Kristin Ritter, MSc, David Schymainski, MSc, Hayley Pomeroy, BSc, Sharon G Lynch, ProfMD, Julia S Cozart, MA, Joan Thelen, PhD, Cristina A F Román, PhD, Margaret Cadden, PhD, Erin Guty, PhD, Stephanie Lau, MSc, Jana Pöttgen, PhD, Caren Ramien, PhD, Susan Seddiq-Zai, MSc, Anna-Maria Kloidt, MSc, Johannes Wieditz, PhD, Iris-Katharina Penner, ProfPhD, Friedemann Paul, ProfMD, Nancy L Sicotte, ProfMD, Jared M Bruce, ProfPhD, Peter A Arnett, ProfPhD, Christoph Heesen, ProfMD |
| Jazyk: |
angličtina |
| Rok vydání: |
2023 |
| Předmět: |
|
| Zdroj: |
The Lancet: Digital Health, Vol 5, Iss 10, Pp e668-e678 (2023) |
| Druh dokumentu: |
article |
| ISSN: |
2589-7500 |
| DOI: |
10.1016/S2589-7500(23)00109-7 |
| Popis: |
Summary: Background: Depression is three to four times more prevalent in patients with neurological and inflammatory disorders than in the general population. For example, in patients with multiple sclerosis, the 12-month prevalence of major depressive disorder is around 25% and it is associated with a lower quality of life, faster disease progression, and higher morbidity and mortality. Despite its clinical relevance, there are few treatment options for depression associated with multiple sclerosis and confirmatory trials are scarce. We aimed to evaluate the safety and efficacy of a multiple sclerosis-specific, internet-based cognitive behavioural therapy (iCBT) programme for the treatment of depressive symptoms associated with the disease. Methods: This parallel-group, randomised, controlled, phase 3 trial of an iCBT programme to reduce depressive symptoms in patients with multiple sclerosis was carried out at five academic centres with large outpatient care units in Germany and the USA. Patients with a neurologist-confirmed diagnosis of multiple sclerosis and depressive symptoms were randomly assigned (1:1:1; automated assignment, concealed allocation, no stratification, no blocking) to receive treatment as usual plus one of two versions of the iCBT programme Amiria (stand-alone or therapist-guided) or to a control condition, in which participants received treatment as usual and were offered access to the iCBT programme after 6 months. Masking of participants to group assignment between active treatment and control was not possible, although raters were masked to group assignment. The predefined primary endpoint, which was analysed in the intention-to-treat population, was severity of depressive symptoms as measured by the Beck Depression Inventory-II (BDI-II) at week 12 after randomisation. This trial is registered at ClinicalTrials.gov, NCT02740361, and is complete. Findings: Between May 3, 2017, and Nov 4, 2020, we screened 485 patients for eligibility. 279 participants were enrolled, of whom 101 were allocated to receive stand-alone iCBT, 85 to receive guided iCBT, and 93 to the control condition. The dropout rate at week 12 was 18% (50 participants). Both versions of the iCBT programme significantly reduced depressive symptoms compared with the control group (BDI-II between-group mean differences: control vs stand-alone iCBT 6·32 points [95% CI 3·37–9·27], p |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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