Efficacy of Posture Correction with MFR on Pulmonary Efficiency in Patients with Kyphosis Deformity
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Forced vital capacity Forced expiratory volume in 1 second 6 minute walk test
研究概览
简要总结
It is a randomised controlled trial with a duration of 3 weeks and involving 30 patients that will be divided into two groups based on lottery method . Its intervention involves thoracic exercise program and myofascial release in one group and only thoracic exercise program in control group . The patient will be informed about the study and written informed consent will be taken . First, each patient’s demographic information including age, height, weight will be gathered as a baseline data. Pre-intervention measurements of outcome variables including Kyphosis angle, Forced expiratory volume in 1 second (FEV1) , Forced vital capacity (FVC) and 6 minutewalk test will be taken. Interventions will be given for 3 weeks then Post- intervention data of all outcome variables will taken.
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 30.00 Year(s)（—）
- 性别
- All
入选标准
- •The kyphosis postural anomaly of more than 42 degree measured by inclinometer.
- •The participants who are giving informed consent for voluntary participation.
排除标准
- •A history of fracture, surgery,joint disease in the vertebral column, shoulder girdle or pelvis.
- •The participants who are unwilling to continue the exercises or absent in two consecutive exercise sessions and absent in measurements sessions.
结局指标
主要结局
Forced vital capacity Forced expiratory volume in 1 second 6 minute walk test
时间窗: The outcome will be assessed for two times which is at the baseline and after 3 weeks
次要结局
- Kyphosis Angle(The outcome will be assessed for two times which is at the baseline and after the 3 weeks)
研究者
Nidhi Kadian
Guru Jambheshwar University of Science and Technology Hisar