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Group-based ACT for Psychological Distress of Young People (ACT-YOUNG)

2026年5月22日 更新者:Sorlandet Hospital HF

This clinical study investigates the effectiveness of two psychological treatment formats for young people aged 16-25 with symptoms of depression, anxiety, stress, or interpersonal difficulties. The study compares group-based Acceptance and Commitment Therapy (ACT) with treatment as usual (TAU), most frequent that would be individual psychotherapy, both of which are established treatment approaches.

The study uses a randomized controlled design (RCT), in which participants are randomly assigned to one of the two treatment conditions. This allows for a systematic comparison of treatment outcomes between ACT delivered in a group format and standard individual therapy.

The ACT group intervention consists of a structured program in which participants meet regularly over a defined treatment period. The treatment focuses on processes such as psychological flexibility, acceptance of internal experiences, and engagement in actions aligned with personal values.

The individual therapy condition consists of one-to-one sessions with a clinician, following standard therapeutic practice. Treatment content and duration are tailored to the participant's clinical presentation and therapeutic needs.

Outcome measures include standardized assessments of mental health symptoms, functioning, and psychological processes. These assessments are conducted at baseline, during the treatment period, at post-treatment, and at follow-up time points. Data collected from these measures will be used to evaluate changes over time and differences between the two treatment conditions.

The primary aim of the study is to determine whether group-based ACT is as effective as, or more effective than, individual psychotherapy for young people receiving mental health services. The results are expected to contribute to improved knowledge about treatment options for this age group and inform future clinical practice.

研究概览

详细说明

Background and Rationale Mental health problems among adolescents and young adults represent a significant and increasing public health concern. A substantial proportion of young people experience symptoms of depression, anxiety, and related psychological distress during a developmental period characterized by major psychological, social, and biological transitions. These challenges may interfere with identity development, educational attainment, and social functioning, with potential long-term consequences for health and well-being .

At the same time, mental health services face increasing demand and limited capacity, resulting in prolonged waiting times and restricted access to timely care. Traditional outpatient treatment is primarily delivered as individual psychotherapy, which limits the number of patients that can be treated. There is therefore a need to evaluate alternative and potentially more scalable treatment formats that can maintain or improve clinical outcomes while increasing accessibility.

Acceptance and Commitment Therapy (ACT) is a transdiagnostic behavioral intervention that aims to improve psychological functioning by enhancing psychological flexibility. The ability to act in accordance with personal values while remaining in contact with difficult internal experiences. Rather than focusing solely on symptom reduction, ACT targets core processes such as acceptance, cognitive defusion, present-moment awareness, values clarification, and committed action.

Although ACT has a substantial evidence base in adult populations, research on its effectiveness for young people remains more limited, particularly in routine clinical settings and in comparison with standard care. Group-based formats may represent an efficient way of delivering ACT, while also offering therapeutic benefits such as peer support, normalization, and shared learning. The present study addresses important gaps in the literature by evaluating a structured group-based ACT intervention tailored for young people, compared with treatment as usual (TAU), within specialized mental health services.

Study Objectives The primary objective of the study is to evaluate the effectiveness of group-based ACT compared with treatment as usual in reducing symptoms of depression and anxiety among young people aged 16-25.

Secondary objectives include:

  • Evaluating the impact of the intervention on psychological well-being, quality of life, and functional outcomes
  • Assessing whether group-based ACT leads to comparable or improved remission rates relative to TAU
  • Investigating mechanisms of change, particularly the role of psychological flexibility related to the ACT processes
  • Exploring potential moderators of treatment outcome, including demographic and clinical characteristics

Study Design

This study is a randomized controlled trial (RCT) with two parallel treatment arms:

  1. Group-based Acceptance and Commitment Therapy (ACT)
  2. Treatment as usual (TAU), typically consisting of individual psychotherapy Participants meeting eligibility criteria will be randomly allocated to one of the two conditions. The study is conducted in routine clinical settings across child/adolescent (BUP) and adult (DPS) mental health services, as well as in collaboration with primary care services, to enhance ecological validity and generalizability .

The target sample size is 212 participants, accounting for expected attrition and ensuring adequate statistical power for both outcome and process analyses .

Participants

Inclusion criteria:

Age 16-25 years Moderate symptoms of depression, score of 14 and above in the DASS 21 questionnaire

Exclusion criteria:

Severe psychiatric conditions requiring alternative treatment (e.g., psychosis, bipolar disorder) Active substance dependence Acute suicidal ideation or behavior Eating disorders or developmental disorders requiring specialized interventions Participants with specific disorders for which established evidence-based treatments are indicated (e.g., OCD) will be offered those treatments outside the study.

Interventions:

Group-based ACT

The experimental intervention is a structured group program based on Acceptance and Commitment Therapy, adapted for young people using the DNA-V framework. The intervention focuses on developing skills in:

  • Awareness of internal experiences
  • Acceptance and willingness
  • Cognitive defusion
  • Values clarification
  • Committed action The group format aims to promote experiential learning and peer interaction. The intervention consists of multiple sessions delivered over a defined treatment period, with each group including up to 10 participants and led by trained therapists. Sessions are manualized to ensure consistency and fidelity, and adherence will be monitored through supervision and video recordings .

Treatment as Usual (TAU) Participants allocated to TAU will receive standard care within mental health services. This typically involves individual psychotherapy delivered by a clinician. The content, frequency, and duration of treatment are determined by clinical needs and routine practice, reflecting real-world conditions.

Procedures and Assessments:

Participants will undergo a baseline assessment prior to randomization, including diagnostic evaluation using structured clinical interviews. Follow-up assessments will be conducted at multiple time points:

  • Baseline (pre-treatment)
  • During treatment (6 weeks)
  • Post-treatment (12 weeks)
  • 6-month follow-up
  • 12-month follow-up

Outcome data will be collected using a combination of clinician-administered interviews and validated self-report measures assessing:

  • Depression and anxiety symptoms
  • General psychological distress
  • Quality of life
  • Functional impairment
  • Psychological processes relevant to ACT (e.g., flexibility, mindfulness, values-based action) In addition to these scheduled assessments, ecological momentary assessment (EMA) will be conducted using a digital platform. Participants will complete brief daily measures during the treatment period and periodic follow-up assessments thereafter. This approach allows for detailed analysis of temporal changes and treatment processes in real-world contexts .

Outcomes

Primary outcomes:

• Changes in symptoms of depression and anxiety

Secondary outcomes:

  • Psychological well-being
  • Quality of life
  • Functional impairment
  • Remission rates

Process outcomes:

  • Psychological flexibility
  • Emotional regulation
  • Mindfulness
  • Self-compassion
  • Values-consistent behavior

Statistical Analysis Data will be analyzed using appropriate statistical methods for longitudinal and randomized designs. Primary analyses will compare changes in outcome measures between treatment conditions over time.

Secondary analyses will examine:

  • Mediation effects to identify mechanisms of change
  • Moderation effects to identify subgroups for whom the treatment is particularly effective Missing data will be handled using established statistical techniques appropriate for repeated measures designs.

Ethical Considerations Participation in the study is voluntary, and all participants will provide informed consent prior to inclusion. Participants may withdraw at any time without consequences for their access to treatment.

The interventions evaluated in this study are based on established therapeutic approaches and are not expected to pose significant risk. However, participation in group-based treatment may be experienced as challenging for some individuals. Measures are in place to monitor and address adverse reactions, including the presence of trained therapists and access to follow-up support .

The study will be conducted in accordance with ethical guidelines and has been approved by the regional ethics committee.

Significance This study will contribute to the evidencebase for psychological treatments for young people by evaluating a scalable, group-based intervention within routine clinical practice. The findings may inform service development and improve access to effective mental health care for this population. Additionally, the study will provide insight into the mechanisms underlying therapeutic change, supporting further refinement of interventions based on ACT principles.

研究类型

介入性

注册 (估计的)

212

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Agder
      • Arendal、Agder、挪威、4824
        • 招聘中
        • Sørlandet hospital
        • 接触:
      • Kristiansand、Agder、挪威、4624
        • 招聘中
        • Sorlandet hospital
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子
  • 成人

接受健康志愿者

描述

Inclusion Criteria:

  • Score on DASS-21 depression scale ≤ 14

Exclusion Criteria:

  • Psychosis

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Group based Acceptance and Commitment Therapy
Participants assigned to this arm will receive a structured, manualized group-based Acceptance and Commitment Therapy (ACT) intervention delivered by trained clinicians.
Group-Based Acceptance and Commitment Therapy (ACT) consists of a structured, manualized group intervention delivered according to established ACT principles and tailored for young people. The intervention is provided in a group format within specialized mental health services and focuses on enhancing psychological flexibility through core ACT processes. Treatment is delivered by trained clinicians, and the group format emphasizes experiential exercises, mindfulness practices, values-based work, and peer interaction. The frequency and duration of sessions follow the study protocol.
有源比较器:Treatment as usual TAU
Participants assigned to this arm will receive treatment as usual consisting of standard mental health care delivered according to routine clinical practice within hospital-based specialized mental health services and, when applicable, municipal health services or student health services. The type, format, frequency, and duration of care are determined by clinical need and may vary between participants.
Treatment as Usual (TAU) consists of standard mental health care provided according to routine clinical practice within hospital-based specialized mental health services, as well as through municipal health services and student health services when applicable. The type, format (e.g., individual or group-based), frequency, and duration of care are determined by clinical need and may vary between participants.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Depression, Anxiety, Stress Scale
大体时间:From enrollment to 1 year
Measures depression, anxiety and stress
From enrollment to 1 year
Hamilton Rating Scale Depression HDRS
大体时间:From enrollment to 1 year
Measures level of depression
From enrollment to 1 year
The Psychological Flexibility Questionnaire PSY-Flex
大体时间:From enrollment to 1 year
Questionnaire measuring Psychological Flexibility
From enrollment to 1 year

次要结果测量

结果测量
措施说明
大体时间
The Structural Clinical Interview for DSM-5 Clinician Version (SCID-5-CV
大体时间:Enrollemnt of study and after 12 months
Diagnostic interview SCID 5 CV
Enrollemnt of study and after 12 months
Clinical Outcomes in Routine Evaluation (CORE-OM)
大体时间:From enrollment to 1 year
Self report about psychological symptoms
From enrollment to 1 year
The PTSD Checklist for DSM-5 PCL-5
大体时间:From enrollment to 1 year
PCL-5 questionnaire, symptoms of PTSD
From enrollment to 1 year
The Level of Personality Functioning Scale brief, LPFS-BF2.0
大体时间:From enrollment to 1 year
The Level of Personality Functioning Scale brief form, Alternative Model for Personality disorders DSM-5, section iii LPFS-BF2.0 questionnaire. Screening tool for personality disorders
From enrollment to 1 year
The Mental Health Continuum short form MHC-SF
大体时间:From enrollment to 1 year
questionnaire that measure positive mental health and well-being
From enrollment to 1 year
Alcohol Use Disorder Identification Test, AUDIT
大体时间:From enrollment to 1 year
Questionnaire screening for alcohol harmful use and dependence
From enrollment to 1 year
The drug use disorders identification test DUDIT
大体时间:From enrollment to 1 year
Questionnaire screening for harmful use and dependence of drugs
From enrollment to 1 year
Difficulties in Emotion Regulation Scale short form DERS SF
大体时间:From enrollment to 1 year
Questionnaire measuring problems with emotion regulations
From enrollment to 1 year
The Cognitive Fusion Questionnaire CFQ
大体时间:From enrollment to 1 year
Questionnaire about cognitive fusion. Cognitive fusion refers to becoming so entangled with thoughts that they strongly dominate behavior, emotions, and perception.
From enrollment to 1 year
The Bulls Eyes Values Survey scale BEVS
大体时间:From enrollment to 1 year
Questionnaire about value congruent behavior. Examening peoples values and how much they are satisfied with reaching those values
From enrollment to 1 year
The Process-Based Assessment Tool PBAT
大体时间:From enrollment to 1 year
Questionnaire measuring processes and clinical interventions in therapy
From enrollment to 1 year
The Five Facet Mindfulness Questionnaire FFMQ
大体时间:From enrollment to 1 year
Questionnaire measuring components and structure of mindfulness
From enrollment to 1 year
The Self Compassion Scale short form SCS SF
大体时间:From enrollment to 1 year
Questionnaire measuring self compassion. Measures of how compassionately a person relates to themselves during periods of difficulty, failure, suffering, or inadequacy.
From enrollment to 1 year
EQ-5D-5L
大体时间:From enrollment to 1 year
EQ EuroQol 5 D 5 Dimensions 5L 5 Levels. Questionnaire used to measure health-related quality of life (HRQoL).
From enrollment to 1 year
The Work and Social Adjustment Scale, WSAS
大体时间:From enrollment to 1 year
Questionnaire that measures how much a person's mental or physical health problems are interfering with their ability to function in everyday life
From enrollment to 1 year
The Bergen Insomnia Scale, BIS
大体时间:From enrollment to 1 year
Questionnaire for measuring insomnia
From enrollment to 1 year
The metacognitions questionnaire, MCQ-30
大体时间:From enrollment to 1 year
Questionnaire about metacognitive beliefs. The beliefs people have about their own thinking
From enrollment to 1 year

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年3月9日

初级完成 (估计的)

2028年12月31日

研究完成 (估计的)

2028年12月31日

研究注册日期

首次提交

2026年5月22日

首先提交符合 QC 标准的

2026年5月22日

首次发布 (实际的)

2026年6月1日

研究记录更新

最后更新发布 (实际的)

2026年6月1日

上次提交的符合 QC 标准的更新

2026年5月22日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • 162090

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

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