Additional Effects of Ujjayi Pranayama on Pulmonary Function in Post Coronary Artery Bypass Graft
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Enrollment
- 36
- Locations
- 2
- Primary Endpoint
- PFT
Study Overview
Brief Summary
Studying the impact of Ujjayi pranayama on post-Coronary Artery Bypass Grafting (CABG) patients has the potential to positively influence healthcare. This research fosters a patient-centered approach, enhancing cardio respiratory function. Patient education on these practices can empower individuals, actively contributing to their recovery and overall well-being.
Detailed Description
. Exercises such as Ujjayi pranayama lower heart rate and benefit high blood pressure sufferers. To determine additional effects of Ujjayi pranayama on pulmonary function in post coronary artery bypass Graft (CABG).
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Outcomes Assessor)
Eligibility Criteria
- Ages
- 35 Years to 60 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Participants who have 1st post op Day
- •Hemodynamically stable & well oriented patient
- •Extubated Patient
- •Voluntary based patients
- •After approval of surgeon CABG patient were recruited
- •Tachypnea
Exclusion Criteria
- •Hemodynamically unstable,
- •Uncontrolled Hypertension,
- •MSK disease,
- •Any previous history of tuberculosis,
- •Neurological disease ,
- •Acute exacerbation of COAD & Asthma Attack,
- •Any trauma, anxiety or Rib fracture case ,
- •During surgery complaint of graft failure ,
- •Unwilling to participate ,
- •Postural Hypotension.
Outcomes
Primary Outcomes
PFT
Time Frame: 5days
Spirometer is simple test used to help diagnose and monitor certain lung conditions by measuring how much air you can breathe out in one forced breathe. Which is a small machine attached by a cable to a mouthpiece. This spirometer yielded generally reproducible results that were generally valid compared to laboratory-based spirometry. The use of this handheld spirometer in clinical, occupational, and research settings seems justified
Borg dyspnea
Time Frame: 5days
(Modified CR-10 is used to assess the degree of dyspnea, rated from 0 to 10. Zero means nothing at all, 0.5=extremely slight, 1=very slight, 2=slight, 3=moderate, 4=somewhat severe, 5=severe, 7=very severe, 9=extremely severe (almost maximal)
Secondary Outcomes
- Cardiac monitors(5days)