Development and Feasibility of a Group-based Psychomotor Intervention for Anxiety in Young Adults
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 12
- 试验地点
- 1
- 主要终点
- Number of participants recruited
研究概览
简要总结
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
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 34 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •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
排除标准
- •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
结局指标
主要结局
Number of participants recruited
时间窗: 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.
Number of participants retained
时间窗: From enrollment to end of intervention at 11 weeks
Attendance
时间窗: From beginning of intervention to end of intervention at 11 weeks
Number of participants attending each of the ten weekly sessions
Acceptability to participants
时间窗: Post intervention at 12 weeks
Evaluated through qualitative interviews with a duration of 45-60 minutes
Fidelity of the intervention
时间窗: 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.
次要结局
- Changes in Beck Anxiety Inventory(Baseline and post-intervention at 11 weeks)
- Changes in Perceived Stress Scale(Baseline and post-intervention at 11 weeks)
- Changes i WHO-Five Well-Being Index(Baseline and post-intervention at 11 weeks)
- Changes in Multiple Assessment of Interoceptive Awareness(Baseline and post-intervention at 11 weeks)