Sjöblom Katja, Frankenstein Katri, Klintwall Lars, Nilbrink Jannike, Zetterqvist Maria, Hesser Hugo, Hedman-Lagerlöf Erik, Gross James J, Hellner Clara, Bellander Martin, Bjureberg Johan
Department of Clinical Neuroscience, Centre for Psychiatry Research, Karolinska Institutet, and Stockholm Health Care Services, Region Stockholm, Stockholm, Sweden.
Department of Child and Adolescent Psychiatry in Linköping, Region Östergötland, and Center for Social and Affective Neuroscience, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.
JAMA Netw Open. 2025 Jun 2;8(6):e2514871. doi: 10.1001/jamanetworkopen.2025.14871.
Mental health problems are common during adolescence, but access to effective treatments is limited. Transdiagnostic treatments could address this treatment gap, but their feasibility, acceptability, and effectiveness remain unknown.
To test the feasibility and acceptability of an online emotion regulation treatment for adolescents with mental health problems and investigate the preliminary effects on clinical outcomes and the target mechanism, emotion regulation.
DESIGN, SETTING, AND PARTICIPANTS: This single-blind randomized clinical trial was conducted between October 16, 2022, and July 28, 2023, in a primary care setting in Sweden. Participants in the intention-to-treat analysis were adolescents aged 12 to 17 years with mental health problems and their parents.
Participants were randomized 1:1 to 6 weeks of therapist-guided online transdiagnostic emotion regulation treatment or an active control condition consisting of 6 weeks of online supportive treatment.
The primary outcomes were feasibility and acceptability measures, including consent rate, completion of assessments, adherence, credibility and expectancy ratings (Credibility/Expectancy Questionnaire), and treatment satisfaction (Client Satisfaction Questionnaire), immediately after treatment. Clinical outcomes, rated by blinded assessor, included global symptom severity and improvement, symptoms of depression and anxiety, global functioning, and emotion regulation.
A total of 30 adolescents (mean [SD] age, 14.2 [1.48] years; 28 females [93%]) were randomized to experimental treatment (n = 15) or active control treatment (n = 15). The consent rate (30 of 37 eligible participants [81%]) and rate of assessment completion immediately after treatment (28 [93%]) were high. Adherence, credibility, expectancy, and satisfaction in both groups were adequate. Participation in the experimental condition, but not the control condition, was associated with large within-group reductions in symptom severity (effect size, 1.30; 95% CI, 0.73-1.86) and symptoms of anxiety and depression (Cohen d, 1.07; 95% CI, 0.37-1.84), improved global functioning (Cohen d, 1.26; 95% CI, 0.66-1.85), and reductions in maladaptive cognitive coping (Cohen d, 1.10; 95% CI, 0.52-1.70) immediately after treatment.
In this randomized clinical trial, a brief online transdiagnostic emotion regulation treatment targeting adolescents with mental health problems was found to be feasible, acceptable, and potentially efficacious in primary care and may increase treatment outreach and accessibility for this population.
ClinicalTrials.gov Identifier: NCT05032547.
心理健康问题在青少年时期很常见,但获得有效治疗的机会有限。跨诊断治疗可以弥补这一治疗差距,但其可行性、可接受性和有效性仍不明确。
测试针对有心理健康问题的青少年的在线情绪调节治疗的可行性和可接受性,并调查其对临床结果和目标机制(情绪调节)的初步影响。
设计、设置和参与者:这项单盲随机临床试验于2022年10月16日至2023年7月28日在瑞典的一家初级保健机构进行。意向性分析的参与者为12至17岁有心理健康问题的青少年及其父母。
参与者按1:1随机分为接受6周治疗师指导的在线跨诊断情绪调节治疗或接受为期6周的在线支持性治疗的积极对照组。
主要结局为可行性和可接受性指标,包括治疗结束后立即的同意率、评估完成情况、依从性、可信度和预期评分(可信度/预期问卷)以及治疗满意度(客户满意度问卷)。由盲法评估者评定的临床结局包括总体症状严重程度和改善情况、抑郁和焦虑症状、总体功能以及情绪调节。
共有30名青少年(平均[标准差]年龄,14.2[1.48]岁;28名女性[93%])被随机分配到实验治疗组(n = 15)或积极对照组(n = 15)。同意率(37名符合条件的参与者中的30名[81%])和治疗结束后立即的评估完成率(28名[93%])很高。两组的依从性、可信度、预期和满意度都足够。参与实验条件组(而非对照组)与治疗结束后立即出现的组内症状严重程度大幅降低(效应量,1.30;95%置信区间,0.73 - 1.86)、焦虑和抑郁症状减轻(科恩d值,1.07;95%置信区间,0.37 - 1.84)、总体功能改善(科恩d值,1.26;95%置信区间,0.66 - 1.85)以及适应不良认知应对减少(科恩d值,1.10;95%置信区间,0.52 - 1.70)相关。
在这项随机临床试验中,针对有心理健康问题的青少年的简短在线跨诊断情绪调节治疗在初级保健中被发现是可行、可接受的,并且可能有效,可能会增加该人群的治疗覆盖面和可及性。
ClinicalTrials.gov标识符:NCT05032547。