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Effectiveness of guided self-help, guided internet-delivered cognitive behavioral therapy, and face-to-face cognitive behavioral therapy for depression and anxiety: protocols of four parallel randomized controlled non-inferiority trials of the Finnish First-Line Therapies –Initiative (FLT-Step)




TekijätHelminen, Eeva-Eerika; Saarni, Suoma E.; Mikkonen, Kasperi; Mattila, M. Katariina; Rosenström, Tom H.; Karukivi, Max; Isometsä, Erkki; Stenberg, Jan-Henry; Ekelund, Jesper; Saarni, Samuli I.

KustantajaBioMed Central

Julkaisuvuosi2026

Lehti: BMC Psychiatry

eISSN1471-244X

DOIhttps://doi.org/10.1186/s12888-026-07962-w

Julkaisun avoimuus kirjaamishetkelläAvoimesti saatavilla

Julkaisukanavan avoimuus Kokonaan avoin julkaisukanava

Verkko-osoitehttps://doi.org/10.1186/s12888-026-07962-w


Tiivistelmä
Background

Low-intensity cognitive behavioral therapy (CBT) based guided self-help (GSH) and guided internet-delivered CBT (GiCBT) have demonstrated equivalent effectiveness and superior cost-efficiency compared to traditional face-to-face CBT (fCBT) for treating depression and anxiety. This study addresses critical gaps in the current understanding of the effectiveness and cost-effectiveness of various CBT interventions for depression and anxiety within a stepped care model.

Methods

We describe a pragmatic multi-center randomized controlled trial (RCT) study with four parallel study protocols (the Finnish First-Line Therapies –Initiative study, FLT-step) for examining three widely used CBT interventions in public healthcare using a stepped care approach according to the FLT-Initiative. The study was preregistered in spring 2024, and participant recruitment began in September 2024. We compare the effectiveness and cost-effectiveness of three treatment approaches for depression (protocol 1) and anxiety (protocol 2) in a non-inferiority setting within the Finnish public healthcare: (A) stepped care (GSH followed by fCBT for non-responders), (B) fCBT, and (C) GiCBT. Non-inferiority margins reflect patient-detectable improvement: 1.7 points on the Patient Health Questionnaire (PHQ-9, protocol 1) and 1.5 points on the Generalized Anxiety Disorder 7-item scale (GAD-7, protocol 2). We plan to recruit 948 adults (≥ 16 years old) with depression (PHQ-9 ≥ 10 p) and 948 adults with anxiety (GAD-7 ≥ 10 p). A randomized substudy will examine the effect of waiting time (≤4 or ≥ 5 weeks) for the treatment outcomes of depression (n = 115, protocol 3) or anxiety (n = 115, protocol 4), comparing the stepped care model (A) and fCBT (B). In all four RCTs, the primary outcome measures are the within-individual change in depression (PHQ-9) or anxiety (GAD-7) symptoms at six months. Secondary outcomes include wellbeing, work and social ability, costs associated with illness, and quality of life. The follow-up will extend up to 20 years. Finnish national registry data will be used to supplement participant data and create population-matched controls to evaluate whether the interventions can prevent clinical episodes, reduce long-term societal costs, and decrease somatic morbidity.

Discussion

This extensive RCT will provide robust evidence on the comparative effectiveness and cost-effectiveness of low-intensity CBT treatments for depression and anxiety, and clarify the impact of waiting times on outcomes.


Julkaisussa olevat rahoitustiedot
Open Access funding provided by University of Helsinki (including Helsinki University Central Hospital). The has received funding from the European Union – NextGenerationEU, Research Council of Finland (372876, 372982, 372878), Department of Psychiatry HUS Helsinki University Hospital (EEH), and The Medical Society of Finland/Finska Läkaresällskapet rf (SES). Roles and responsibilities—sponsor and funder. Funders or organizational sponsors had no role in the design of this study and will not have any role in the data management, analyses and interpretation of the data, nor in the decision to submit the reports for publication. The study is coordination is led by PI, supported by the research team. No additional formal steering committee is established as this is a pragmatic, researcher-initiated trial conducted within routine public health care services and poses minimal risk. Data management is overseen by the research team, with institutional support from the respective wellbeing services counties and HUS. Outcomes are collected using validated self-report instruments or registry data, minimizing the need for external adjudication.


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