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RecruitingNCT07872098Updated Oct 13, 2026

Effects of Pilates Breathing Versus Diaphragmatic Breathing on Oxygen Saturation and Heart-Rate Variability in Post-Percutaneous Coronary Intervention Patients

An interventional study of Pilates Breathing and Diaphragmatic breathing in Oxygen Saturation and Percutaneous Coronary Intervention, sponsored by Foundation University Islamabad. Recruiting at 1 site in Pakistan. Open to participants aged 44 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-10-13.

Sponsored by Foundation University Islamabad · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 7 months after the study started (first participant enrolled Feb 2026, registered Oct 2026).
  • Started Feb 2026; still recruiting 8 months later.
Updated Oct 13, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Randomized
Ages
44 Years to 75 Years
Sex
All
01

Study summary

Percutaneous Coronary Intervention (PCI) is a common procedure used to restore coronary blood flow in patients with coronary artery disease. Post-PCI patients may experience reduced exercise tolerance, altered breathing patterns, and autonomic imbalance, which may affect oxygen saturation and heart-rate variability (HRV). Breathing exercises are simple, non-pharmacological interventions that may support early recovery. This randomized controlled trial aims to compare the effects of Pilates breathing and diaphragmatic breathing on oxygen saturation and HRV in hemodynamically stable post-PCI patients. A total of 36 participants will be randomly allocated into two groups using a sealed opaque envelope method. The Pilates breathing group and diaphragmatic breathing group will receive supervised breathing exercises for 2 consecutive days, with three sessions per day, in addition to routine care. Oxygen saturation will be assessed using a pulse oximeter, while HRV will be measured using a Polar H10 chest belt. Pre- and post-intervention measurements will be compared between the two groups.

Read the detailed description

Percutaneous Coronary Intervention (PCI) is a commonly performed procedure for restoring coronary blood flow in patients with coronary artery disease. Following PCI, patients may experience altered breathing patterns, reduced exercise tolerance, and changes in autonomic cardiovascular regulation, which may influence oxygen saturation and heart-rate variability (HRV) during the early recovery period. Breathing exercises are simple, safe, and non-pharmacological interventions that can be incorporated into early cardiac rehabilitation. This study aims to compare the effects of Pilates breathing and diaphragmatic breathing on oxygen saturation and heart-rate variability in hemodynamically stable patients following PCI. The study will be conducted as a parallel-arm randomized controlled trial at Fauji Foundation Hospital, Rawalpindi. A total of 36 participants will be recruited through non-probability purposive sampling and randomly allocated into two groups using sealed opaque envelopes. The Pilates breathing group will receive supervised Pilates breathing exercises, while the diaphragmatic breathing group will receive supervised diaphragmatic breathing exercises. Both groups will undergo the intervention for two consecutive days, with three sessions per day. On Day 0, each session will last 15 minutes and include 10 repetitions, while on Day 1, each session will last 20 minutes and include 15 repetitions. Routine care will continue alongside the breathing interventions. Oxygen saturation (SpO2) will be assessed using a pulse oximeter, while heart-rate variability will be measured using a Polar H10 chest belt/ECG-based HRV assessment. Heart rate, blood pressure, respiratory rate, and oxygen saturation will be monitored before and after each session. Participants will be kept blinded to group allocation. The study will include hemodynamically stable post-PCI patients aged 44-75 years who meet the predefined eligibility criteria, including SpO2 ≥92% on room air and ejection fraction greater than 35%. Patients with ongoing myocardial ischemia, unstable angina, significant arrhythmias, cardiogenic shock, severe heart failure, severe cognitive impairment, uncontrolled hypertension, severe anemia, or other specified exclusion criteria will not be included. The primary outcome will be oxygen saturation, while heart-rate variability will be assessed as a secondary outcome. The study findings will help determine the effects of Pilates breathing and diaphragmatic breathing on oxygen saturation and autonomic cardiovascular regulation during early post-PCI recovery.

02

Conditions studied

  • Oxygen Saturation
  • Percutaneous Coronary Intervention

Keywords

  • Pilates breathing
  • Diaphragmatic breathing
  • Heart rate variability
03

In context

Lead sponsor

Foundation University Islamabad is the lead sponsor of 253 studies on the registry; 140 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
44 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 44-75 years (> 75 years as an "at-risk" group) (20).
  • Hemodynamically stable: SBP >90 mmHg, DBP 50-100 mmHg, HR 60-100 bpm, and no ongoing chest pain or signs of acute.
  • Oxygen saturation SpO₂ ≥ 92% on room air
  • Able to follow simple verbal instructions and perform breathing exercises.
  • Ejection fraction >35%

Exclusion criteria

Exclusion Criteria:

  • Ongoing myocardial ischemia, unstable angina, significant arrhythmia or requirement for inotropic/vasopressor
  • Cardiogenic shock or severe heart failure (NYHA IV)
  • Recent thoracic surgery or chest wall injury that limits rib expansion
  • Presence of cardiac implantable electronic device (pacemaker/ICD) with pacing dependency, or implanted ventricular assist device
  • Severe cognitive impairment.
  • Uncontrolled hypertension (SBP > 180 mmHg or DBP > 110 mmHg) or bradycardia \< 50.
  • Severe anemia (Hb \< 8)
  • Pregnancy.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
36 participants (estimated)

Study arms

  • Experimental
    Pilates Breathing group A

    Supervised Pilates breathing. Post-op Day 0: 3 sessions/day, 15 minutes/session, 10 repetitions. Post-op Day 1: 3 sessions/day, 20 minutes/session, 15 repetitions. Pre- and post-session HR, BP, RR and SpO2 will be monitored. Intervention is provided in addition to routine care.

    Procedure: Pilates Breathing

  • Active comparator
    Diaphragmatic Breathing group B

    Supervised diaphragmatic breathing. Post-op Day 0: 3 sessions/day, 15 minutes/session, 10 repetitions. Post-op Day 1: 3 sessions/day, 20 minutes/session, 15 repetitions. Pre- and post-session HR, BP, RR and SpO2 will be monitored. Intervention is provided in addition to routine care.

    Procedure: Diaphragmatic breathing

Interventions

  • ProcedurePilates Breathing

    Pilates breathing is a controlled breathing technique that involves lateral rib cage expansion during inhalation and slow, active exhalation. The intervention will be administered under physiotherapist supervision for 2 consecutive days with three sessions per day in addition to routine post-PCI care.

  • ProcedureDiaphragmatic breathing

    A deep breathing method that uses the diaphragm with minimal chest movement, performed in a controlled manner for a set duration. The intervention will be performed under physiotherapist supervision in addition to routine post-PCI care

06

What researchers measure

Primary outcomes

  1. Oxygen Saturation

    Oxygen saturation will be measured using a pulse oximeter before and after the intervention to compare the effects of Pilates breathing and diaphragmatic breathing in post-PCI patients.

    Time frame: Baseline and immediately after the 2-day intervention period

  2. Heart-Rate Variability

    Variation in time between consecutive heartbeats measured using a Polar H10 chest belt/ECG-based heart-rate sensor.

    Time frame: Baseline and immediately after the 2-day intervention period.

07

Study locations

1 of 1 sites recruiting
  • Foundation University Islamabad
    Rawalpindi, 46000, Pakistan
    Recruiting
08

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 13, 2026
Show all 1 update
  1. Oct 13, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07872098
Responsible party
Sponsor
First posted
Oct 13, 2026
Start date
Feb 11, 2026
Primary completion
Dec 15, 2026 (estimated)
Completion
Dec 15, 2026 (estimated)
Last update
Oct 13, 2026

Study contacts

Aqsa Kanwal Siddique, MS-CPPT
Contact
Itsaqsa025@gmail.com
03315874402
Sana Bashir, MS-CPPT
Contact
drsana.bashir@fui.edu.pk
03218529475

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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