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临床试验/CTRI/2019/06/019761
CTRI/2019/06/019761尚未招募不适用

Efficacy of alternate nostril breathing on pulmonary functions and physical functional capacity in healthy adults across different age groups

MMIPR1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2019年8月20日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
64
试验地点
1
主要终点
Spirometer

研究概览

简要总结

Background:

Alternate nostril breathing is a breathing technique in which both the nostrils are used alternately to inhale and exhale to complete a respiratory cycle.Objective:

To evaluate the effect of alternate nostril breathing on forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC), FEV1/FVC, peak expiratory flow rate (PEFR), peak inspiratory flow rate (PIFR), distance covered during 6 minutes walk test and rate of perceived exertion in healthy adults across different age groups.

Method:

Male and female patients of 20-50 years of age will be selected based on subject selection criteria. The samples will be taken by stratified random sampling and divided them into two stratas of different age groups. Then by randomization , both strata will divide into control and experimental groups. Experimental groups of both strata will receive alternate nostril breathing exercise for 15 minutes daily in morning for 4 weeks, while the control group will not perform anything. Measurement of FEV1, FVC, FEV1/FVC, PEFR, PIFR, distance covered during 6 minutes walk test and rate of perceived exertion will be recorded at baseline and after 4 weeks of intervention.

Result:

Data will be collected , entered and analysed by primary researcher. Normality test will be used to measure the normal distribution of data. Data will be analysed using SPSS version 21.0.  Level of significance will be set as 0.05.

Conclusion:

The present study will provide information about the efficacy of alternate nostril breathing on pulmonary funtion and physical funtional capacity in healthy adults across different age groups.

Keywords:

Alternate nostril breathing, pulmonary function, functional capacity.

研究设计

研究类型
Interventional
分配方式
Permuted block randomization, fixed
盲法
Participant Blinded

入排标准

年龄范围
20.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • •1.Healthy individual between 20-50 years of age.
  • •2.Sedentary life style.
  • •3.Voluntary participants.

排除标准

  • •1.Smokers & alcoholics.
  • •2.Cardio-pulmonary disorders.
  • •4.Hypertension.
  • •5.Neurological disorders.
  • •6.Musculoskeletal disorders.
  • •7.Body Mass Index ≥23 kg/m2 (Asia-pacific BMI).

结局指标

主要结局

Spirometer

时间窗: Outcome will be measured before and after 4 weeks of treatment. intervention will be given for 15 minutes daily for 4 weeks during morning

次要结局

  • Distance covered during 6 minutes walk test , Rate of perceived exertion on Modified Borgs scale(Outcome will be measured before and after 4 weeks of treatment. Intervention will be given for 15 minutes daily for 4 weeks during morning.)

研究者

发起方
MMIPR
申办方类型
Private medical college

研究点 (1)

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