None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: non-smokers individuals with normal BMI Individuals having sedentary lifestyle subjects who understand verbal English language and willing to give consent to participate
Exclusion criteria
Exclusion criteria: Subjects with h/o of any conditions which can affect the outcome of the study: Musculoskeletal disorder, Cardiovascular disorder, Respiratory disorder, Neurophysiologic disorder Any other known medical/physical/surgical/traumatic conditions. Subjects on any regular medication which can affect the outcome of the study. Pregnant females
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| chest expansion pulmonary function (FEV1), (FVC), FEV1/FVC ratio by PFT aerobic capacity (VO2 max) by arm ergometry Heart rate recovery (HRR) and blood pressureTimepoint: Baseline (before the start of intervention) On 5th day On 10th day On 15th day On 20th day On 25th day | — |
Secondary
| Measure | Time frame |
|---|---|
| Scapula position (Lateral scapula slide test)Timepoint: Baseline (before the start of intervention) On 5th day On 10th day On 15th day On 20th day On 25th day;Forward head posture (craniovertebral angle)Timepoint: Baseline (before the start of intervention) On 5th day On 10th day On 15th day On 20th day On 25th day | — |
Countries
India
Contacts
Delhi Pharmaceutical Sciences and Research University