Effects of Short-Term Conscious Awareness-Based Cognitıve Therapy Applied to Asthma Patients on Anxiety, Depression and Dyspnea
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 48
- 试验地点
- 2
- 主要终点
- Anxiety
研究概览
简要总结
In this study, short-term MBCT will be applied to asthmatic patients receiving hospital treatment and its effects on anxiety, depression and dyspnea will be determined. A quasi-experimental study was planned for this purpose.
详细描述
In the study, cognitive behavioral therapy will be applied to the intervention group, which is determined as the experimental group, and a group of asthma patients who did not receive any application during the same periods will be included and the dyspnea, anxiety and depression levels of the patients in these two groups will be compared.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Single (Outcomes Assessor)
盲法说明
Participants and researchers could not be blinded due to the natural course of the study and only the statistician was blinded.
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Over 18 years old, Inpatient treatment in the chest ward volunteer participants with no communication problems
排除标准
- •Under 18 years old, with communication problems, not willing to participate hospitalized with diseases other than asthma
研究组 & 干预措施
Experimental group
In this study, it is planned to apply MBCT to asthmatic inpatients in the patient room in groups of 2 or 3. This application is planned to continue for one hour.
干预措施: mindfulness-based cognitive therapy (Other)
Control group
No application will be made to the patients in the control group.
干预措施: routine treatment and care (Other)
结局指标
主要结局
Anxiety
时间窗: Average of 1 week after completion of the intervention
It will be evaluated with the Hospital Anxiety and Depression Scale.
Depression
时间窗: Average of 1 week after completion of the intervention
It will be evaluated with the Hospital Anxiety and Depression Scale.
Dyspnea
时间窗: Average of 1 week after completion of the intervention
It will be assessed with the Modified Medical Research Council (mMRC) Dyspnoea Questionnaire.
次要结局
未报告次要终点