Health TrialsbyHealthPanel

Additional Effects of Ujjayi Pranayama

ConditionsPulmonary FunctionCoronary Artery Disease
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age35-60
SponsorRiphah International University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Participants who have 1st post op Day

Hemodynamically stable & well oriented patient

Extubated Patient

Voluntary based patients

Disqualifiers

Hemodynamically unstable,

Uncontrolled Hypertension,

MSK disease,

Any previous history of tuberculosis,

Trial design

Design model

Parallel

Treatments tested in this trial

  • Ujjayi Paranayama

    Other intervention

    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

  • Standard Protocol

    Other intervention

    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

Treatment groups

36 Participants
are divided into 2 treatment groups
Group A: arm:1 PranayamaExperimental treatment 1 intervention
Group B: arm: 2 (standard protocol)Other 1 intervention

Trial outcomes

Primary outcomes

1

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)

Time frame
5days
2

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

Time frame
5days

Secondary outcomes

1

Cardiac monitors

After 5, 10, 15, 20, and 30 minutes of pranayama in the study group and without pranayama in the control group, recordings of HR, SBP, DBP, RR, SpO2

Time frame
5days

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Riphah International University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: