A Psychomotor Group Intervention for Young Adults With Anxiety Symptoms
2026年6月25日 更新者：VIA University College
Development and Feasibility of a Group-based Psychomotor Intervention for Anxiety in Young Adults
The goal of this clinical trial is to learn if a psychomotor (a body-oriented therapy) group intervention can be feasibly delivered to a group of young adults (age 18-35) with anxiety symptoms within a higher educational setting.
The main questions it aims to answer are:
- Is it possible to recruit and retain participants in this intervention?
- Is the intervention acceptable and tolerable to participants?
- Do participants complete the planned sessions and assessments?
Participants will:
- Attend one weekly group session over ten consecutive weeks
- Participate in active and contemplative body-based exercises
- Complete questionnaires about their mental health and interviews about their experiences of participating
研究概览
地位
完全的
条件
研究类型
介入性
注册 (实际的)
12
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。
学习地点
-
-
Region Midt
-
Aarhus、Region Midt、丹麦、8200
- VIA University College
-
-
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
- 成人
接受健康志愿者
不
描述
Inclusion Criteria:
- Age between 18 and 34 years
- A score of at least 2 on item 10 of the Anxiety Symptom Scale (indicating the perceived strain of the experienced anxiety symptoms) and at least 1 on one or more of items 1-3 (generalized anxiety symptoms and avoidance behavior)
- Sufficient Danish language proficiency to participate in group sessions and interviews
Exclusion Criteria:
- Physical or psychological conditions that prevents participation in group-based or bodily-activities, such as significant musculoskelatal impairment or current, untreated episodes of psychosis
- Ongoing alcohol or substance abuse
- Concurrent participation in another body-oriented intervention program
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：不适用
- 介入模型：单组作业
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的：Psychomotor intervention group
|
Ten weekly sessions of a psychomotor therapy group program.
Session duration: 2½ hours.
Group size: 12 participants.
Sessions include psychoeducational content and body-oriented exercises such as breathing exercises, relaxation exercises, body scans, or grounding exercises.
|
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 |
|---|---|---|
|
Number of participants recruited
大体时间：For each participant: 20 minutes during the three month enrollment period.
|
Enrollment during a three month period from June 2025 to September 2025.
Enrollment interview was approximately 20 minutes.
Participants had the option of attending a one hour information meeting.
|
For each participant: 20 minutes during the three month enrollment period.
|
|
Number of participants retained
大体时间：From enrollment to end of intervention at 11 weeks
|
From enrollment to end of intervention at 11 weeks
|
|
|
Attendance
大体时间：From beginning of intervention to end of intervention at 11 weeks
|
Number of participants attending each of the ten weekly sessions
|
From beginning of intervention to end of intervention at 11 weeks
|
|
Acceptability to participants
大体时间：Post intervention at 12 weeks
|
Evaluated through qualitative interviews with a duration of 45-60 minutes
|
Post intervention at 12 weeks
|
|
Fidelity of the intervention
大体时间：From beginning of intervention to end of intervention at 11 weeks
|
The extent to which intervention components were administered as intended.
This was registered by an observer who registered any deviations from a therapy manual.
|
From beginning of intervention to end of intervention at 11 weeks
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Changes in Beck Anxiety Inventory
大体时间：Baseline and post-intervention at 11 weeks
|
21 items rated on a four-point Likert scale with scores ranging rom 0 (no anxiety) to 21 (worst possible anxiety)
|
Baseline and post-intervention at 11 weeks
|
|
Changes in Perceived Stress Scale
大体时间：Baseline and post-intervention at 11 weeks
|
Ten items rated on a five-point Likert scale with scores ranging from 0 (no stress) - 40 (maximum stress)
|
Baseline and post-intervention at 11 weeks
|
|
Changes i WHO-Five Well-Being Index
大体时间：Baseline and post-intervention at 11 weeks
|
A five-item measure rated on a six-point Likert scale with scores ranging from 0 (worst possible well-being) to 100 (maximum well-being)
|
Baseline and post-intervention at 11 weeks
|
|
Changes in Multiple Assessment of Interoceptive Awareness
大体时间：Baseline and post-intervention at 11 weeks
|
Body awareness measured through 32 items across eight subscales rated on a six-point Likert scale, reported as mean scores on each subscale (range 0-5)
|
Baseline and post-intervention at 11 weeks
|
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。
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)
2025年9月12日
初级完成 (实际的)
2025年12月18日
研究完成 (实际的)
2025年12月18日
研究注册日期
首次提交
2026年6月12日
首先提交符合 QC 标准的
2026年6月25日
首次发布 (实际的)
2026年7月2日
研究记录更新
最后更新发布 (实际的)
2026年7月2日
上次提交的符合 QC 标准的更新
2026年6月25日
最后验证
2026年6月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.