Effect of Nordic Walking During Cardiac Rehab on cardiopulmonary parameters in post-op CABG: A Randomised Clinical Trial
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Chest Expansion, Respiratory Rate, Resting Heart Rate, blood pressure, and Hand grip strength
研究概览
简要总结
Nordic walking—a form of walking with specially designed poles which engages the upper body and improves walking efficiency and cardiovascular fitness, making it a beneficial addition to rehabilitation programmes. A randomised clinical trial will be conducted to explore the effects of cardiac rehabilitation incorporating Nordic walking on functional capacity and cardiopulmonary parameters in post-CABG patients. Initially, 30 subjects will be recruited by a convenient sampling method and then will be randomly allocated to two groups. An informed consent form will be obtained from the subjects. The intervention will be given for 15 days. A total of 15 sessions will be given in both groups. Pre-intervention assessment of chest expansion, resting heart rate, blood pressure, respiratory rate, hand grip strength, 6-minute walk distance, sleep quality, depression, anxiety, and stress will be conducted. Post-intervention evaluation for the same parameters will be done again by the end of the 5th, 10th, and 15th day, respectively. All the data will be compiled and statistically analysed to determine the effectiveness of Nordic walking on selected parameters in post-op CABG patients.
研究设计
- 研究类型
- Interventional
- 分配方式
- Other
- 盲法
- None
入排标准
- 年龄范围
- 40.00 Year(s) 至 65.00 Year(s)（—）
- 性别
- All
入选标准
- •Elective CABG surgery 2.LVEF percentage:more than 30 percent 3.NHYA classification: Class one and two 4.Subjects who understand Hindi and/or English are willing to give consent to participate.
排除标准
- •1.Unstable Angina Pectoris 2.Uncontrolled arrhythmias 3.Renal failure 4.Any life-threatening co-morbidities 5.Any locomotor or neurological disability (it may hamper the functional performance of the subject) History of prior cardiac surgery, stroke, and pulmonary diseases (COPD, Asthma, TB, etc.) that can affect the outcome of the study 6.Active communicable disease.
结局指标
主要结局
Chest Expansion, Respiratory Rate, Resting Heart Rate, blood pressure, and Hand grip strength
时间窗: At Baseline (before the start of intervention) | On Postoperative Day 5 (after 5 sessions) | On Postoperative Day 10 (after 10 sessions) | On Postoperative Day 15 (after 15 sessions)
次要结局
- Functional capacity (6MWD), Sleep quality (PSQI), & Depression, Anxiety, & Stress (DASS-21)(At Baseline (before the start of intervention))
- Pain (NPRS)(At Baseline (before the start of intervention))
研究者
Prashansa Jain
Delhi Pharmaceutical Sciences and Research University