Additional Effects of Ujjayi Pranayama

NCT06663800 | Not Yet Recruiting

• 1 other identifier: REC/MSPT0193 Kulsoom
• Study Type: interventional
• Target: 36
• Locations: 1 country
• Sites: 1

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.

Conditions

Pulmonary Function; Coronary Artery Disease

Keywords

Ujjayi Paranyama; Coronary artery bypass grafting; Pulmonary Function

Outcome Measures

Primary Outcomes (2)

• Borg dyspnea

  (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)

  5days

• PFT

  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

  5days

Secondary Outcomes (1)

• Cardiac monitors

  5days

Study Arms (2)

arm:1 Pranayama

EXPERIMENTAL

Arm:1 Additional effects of Ujjayi Pranayama

Other: Ujjayi Paranayama

arm: 2 (standard protocol)

OTHER

Arm:2 (standard protocol)

Other: Standard Protocol

Interventions

Ujjayi Paranayama OTHER

Inhale or breathe in slowly while taking a deep, prolonged breath through both nostrils. As you inhale, attempt to tighten your throat and feel the air in your throat. Air should not come into contact with the interior of the nose. When air enters the throat, an odd sound is made. Allow the breath to be loose and easy while you slightly tighten the back of your throat and hiss lightly as you breathe in and out. The sound isn't forced, but it should be loud enough for someone to hear you if they were close. Now close your right nostril and release the breath through your left. As you exhale, try making the sound HHHHHAAAA

arm:1 Pranayama

Standard Protocol OTHER

Control Group will perform Deep Breathing Adhering to a FITT model protocol, with a frequency of 5 days. Intensity set at 8 repetitions, duration range from 10 to 15 minutes

arm: 2 (standard protocol)

Eligibility Criteria

• Age: 35 Years - 60 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• 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

You may not qualify if:

• 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.

Sponsors & Collaborators

• Riphah International University: lead

Study Sites (1)

Railway general hospital

Rawalpindi, Punjab Province, 46060, Pakistan

Location

MeSH Terms

Conditions

Coronary Artery Disease

Interventions

AIEOP acute lymphoblastic leukemia protocol

Condition Hierarchy (Ancestors)

Coronary Disease; Myocardial Ischemia; Heart Diseases; Cardiovascular Diseases; Arteriosclerosis; Arterial Occlusive Diseases; Vascular Diseases

Study Officials

• Maria Razzaq, MSCPPT

  Riphah International University

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Maria Razzaq, MSCPPT

CONTACT

03431597909; maria.razzaq@riphah.edu.pk

Iqbal Tariq, MSCPPT

CONTACT

iqbal.tariq@riphah.edu.pk

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 23, 2024
• First Posted: October 29, 2024
• Study Start: October 28, 2024
• Primary Completion: December 15, 2024
• Study Completion: January 18, 2025
• Last Updated: October 29, 2024

Record last verified: 2024-10

Data Sharing

• IPD Sharing: Will not share

Locations

PA (1)