跳至主要内容
临床试验/NCT07635446
NCT07635446招募中不适用

Effects of Laura Mitchell's and Benson Relaxation Technique On Anxiety, Sleep Quality and Fatigue Among COPD Patients

Riphah International University1 个研究点 分布在 1 个国家目标入组 38 人开始时间: 2026年6月1日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
38
试验地点
1

研究概览

简要总结

Chronic Obstructive Pulmonary Disease (COPD) is a progressive lung condition characterized by persistent respiratory symptoms and airflow limitation. Patients with COPD often experience not only physical symptoms like breathlessness and fatigue but also psychological issues such as anxiety and poor sleep quality, which further compromise their quality of life. Non-pharmacological interventions, especially relaxation techniques, have shown promise in improving psychological well-being and physiological outcomes in COPD patients. Among these, Laura Mitchell's relaxation technique and Benson's relaxation response have gained attention for their simplicity and effectiveness.

The primary objective of this study is to assess and compare the effects of Laura Mitchell's relaxation technique and Benson's relaxation technique on anxiety, sleep quality, and fatigue levels in patients diagnosed with moderate to severe COPD. By evaluating these parameters, the study aims to determine which method provides greater benefits in managing psychological and physical symptoms associated with COPD. The study will use a randomized experimental design. Participants will be randomly assigned into two groups: Group A will receive Laura Mitchell's relaxation training, and Group B will receive Benson's technique. Both interventions will be practiced daily for 15-20 minutes over a 6-weeks period. Baseline and post-intervention (week 6) data will be collected. Outcome measures will include anxiety (GAD-7), fatigue (FSS) and sleep quality (PSQI). Data will be analyzed using paired and independent t-tests to assess within-group and between-group differences, with significance set at p < 0.05. The data will be analyzed using SPSS v 25.

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
Double (Participant, Investigator)

盲法说明

None (Open Label) Because of the physical nature of the interventions, both participants and investigators will know which treatment is being given. No blinding will be applied.

入排标准

年龄范围
40 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • - Gender: Male and Female
  • Age: 40 to 60 years
  • Patients diagnosed with COPD
  • Willing to participate

排除标准

  • Patients with Exacerbations within past 4 weeks
  • Cardiac Diseases (Acute MI, Congestive Heart Failure)
  • Neuromuscular Disorder
  • Recent lung diseases
  • Hemodynamic instability
  • Respiratory failure

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验