High Intensity Training for Patients with Anxiety
试验速览
- 阶段
- 不适用
- 状态
- Enrolling By Invitation
- 发起方
- 入组人数
- 26
- 试验地点
- 1
- 主要终点
- Anxiety
研究概览
简要总结
The aim of the current project is to examine the effects of high intensity exercise (by using 1x4 intervals) to reduce symptoms of anxiety in patients in mental health care. The expected benefits for patients are positive health effects, by improving physical fitness and reducing psychological symptom burden. The patients will have the opportunity to learn to use physical activity as a specific measure to be used in their own lives and be a source of coping. Furthermore, knowledge about physical activity and mental health may be applicable in mental health care as a part of a treatment plan.
详细描述
The study is a randomised controlled trial ("RCT") design with a 1:1 allocation into two groups. The two groups are high intensity exercise (1x4 minutes performed two times per week with a heart rate above 85% of maximal heart rate) and low intensity exercise (45 minutes performed two times per week with a heart rate of approximately 60% of maximal heart rate). The total amount of training sessions for both groups will be eight. The high intensity exercise group will serve as the intervention group, while the low intensity exercise group will serve as an active control group.
The patients will be randomly allocated (randomised) to these groups. An exercise physiologist (holding a master's degree in exercise physiology) will supervise the training sessions. The training sessions will take place in a dedicated room using a treadmill and a heart rate monitor. The training sessions will be individual.
The primary outcome measure will be degree of anxiety symptoms measured by Hospital Anxiety and Depression Scale (HADS) and Beck Naxiety Inventory (BAI) prior to the first (pre) and after the last (post) training session is completed. Secondary outcome measures will be compliance, i.e. to what degree the patient is able to sustain the exercise regimen three months after participating in the project, in addition to the patient's blood pressure.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with mild/moderate anxiety disorders, aged 18-60 years. Anxiety disorders in accordance with F 41 in ICD-10, including generalised anxiety disorder, agoraphobia/panic disorder, social phobia, post-traumatic stress disorder, hypochondria, and obsessive-compulsive disorder.
- •Comorbidity will occur, so the patient may also have depression. However, the main disorder should be anxiety.
排除标准
- •Somatic diseases that may impede training: cardiovascular disease, severe asthma, severe COPD, cancer, poorly regulated diabetes.
- •Schizophrenia or bipolar disease
- •Suicidality (prior attempts or ongoing risk of suicide)
- •Substance addiction
研究组 & 干预措施
High intensity exercise training
High intensity exercise training
干预措施: Exercise (Behavioral)
Low intensity exercise training
Low intensity exercise training
干预措施: Exercise (Behavioral)
结局指标
主要结局
Anxiety
时间窗: HADS will be performed on the first day the patient attends the study and on the very last day the patient attends.
Hospital Anxiety and Depression Scale (HADS). This a questionnaire generating a scale ranging from 0 to 42 points. Lower scores mean a better outcome.
次要结局
- Systolic and diastolic blood pressure(We will measure the blood pressure on the first day the patient attends the study and on the very last day the patient attends.)
- Beck Depression Inventory(Beck Depression Inventory will be performed on the first day the patient attends the study and on the very last day the patient attends.)
研究者
Martin Kragnes Bystad
Head of research
University Hospital of North Norway