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RecruitingNCT07591987Updated May 18, 2026

Effect of Different Breathing Techniques on Dyspnea and Cardiopulmonary Parameters Among Patients After Open Heart Surgery

An interventional study of Segmental Breathing Exercises and Active Cycle Breathing Technique in Dyspnea, Cardiopulmonary Dysfunction and Postoperative Respiratory Dysfunction, sponsored by University of Baghdad. Recruiting at 3 sites in Iraq. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-05-18.

Sponsored by University of Baghdad · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jul 2026, 4 months ago, but the record still lists the study as recruiting.
  • Registered 4 months after the study started (first participant enrolled Jan 2026, registered May 2026).
  • Started Jan 2026; still recruiting 10 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
99
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

Open heart surgery is often associated with postoperative pulmonary complications, reduced lung expansion, dyspnea, and impaired cardiopulmonary function. Breathing exercises are commonly used after surgery to improve lung ventilation, enhance oxygenation, and support respiratory recovery. However, limited evidence is available comparing the effectiveness of segmental breathing exercises and active cycle breathing technique (ACBT) in patients after open heart surgery.

This randomized controlled trial will compare the effects of segmental breathing exercises and ACBT on dyspnea and cardiopulmonary parameters in adults undergoing open heart surgery. Participants will be randomly assigned to either the segmental breathing exercise group, the ACBT group, or the standard care group during the postoperative period following extubation.

Cardiopulmonary parameters, including oxygen saturation, respiratory rate, heart rate, and blood pressure, as well as dyspnea severity and postoperative pulmonary complications, will be assessed before and after the interventions.

The findings of this study may help identify the most effective breathing exercise technique for improving respiratory outcomes, reducing postoperative pulmonary complications, and supporting evidence-based postoperative rehabilitation after cardiac surgery.

Read the detailed description

This randomized clinical trial evaluates the effects of segmental breathing exercises (SBE) and active cycle breathing technique (ACBT) on dyspnea, cardiopulmonary parameters, and postoperative pulmonary complications in adults undergoing elective open-heart surgery with cardiopulmonary bypass.

Participants will be randomly assigned to one of three groups: segmental breathing exercises group, active cycle breathing technique group, or standard care group. Patients in the intervention groups will perform the assigned breathing exercises after extubation, including sessions conducted 1 hour and 6 hours post-intervention during the early postoperative period.

Cardiopulmonary parameters, including oxygen saturation, respiratory rate, heart rate, and blood pressure parameters, will be monitored throughout hospitalization. Dyspnea and postoperative pulmonary complications, including atelectasis and pneumonia, will also be assessed.

The primary purpose of this study is to determine the effectiveness of breathing exercise interventions in improving postoperative respiratory outcomes and reducing pulmonary complications after cardiac surgery. The study also aims to support evidence-based postoperative rehabilitation practices for healthcare professionals caring for patients after open-heart surgery.

02

Conditions studied

  • Dyspnea
  • Cardiopulmonary Dysfunction
  • Postoperative Respiratory Dysfunction
  • Coronary Artery Disease

Keywords

  • Open Heart Surgery
  • Cardiac Surgery
  • Breathing Exercises
  • Segmental Breathing Exercises
  • Active Cycle Breathing Technique
  • Postoperative Patients
  • Adult Patients
  • Dyspnea
  • Cardiopulmonary Parameters
03

In context

Dyspnea

894 studies on the registry are indexed under Dyspnea; 189 are open to participants now.

This study's planned enrollment of 99 is above the median of 50 across 587 interventional studies indexed under Dyspnea.

Browse Dyspnea studies →

Lead sponsor

University of Baghdad is the lead sponsor of 170 studies on the registry; 69 are open to participants now.

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

04

Who can participate

Ages eligible
18 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 18-75 years.
  • Scheduled for elective open-heart surgery.
  • Can understand instructions and perform Segmental breathing and Active cycle breathing techniques.
  • Stable preoperative hemodynamic condition.

Exclusion criteria

Exclusion Criteria:

  • Emergency cardiac surgeries.
  • Patients with pre-existing severe pulmonary disease (e.g., , asthma, restrictive lung disease, Atelectasis, and Tuberculosis).
  • Neurological disorders affecting breathing effort.
  • Patients with rib fractures, recent thoracic trauma, or for coughing maneuvers.
  • Inability to provide (cognitive impairment, language barrier).
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

COPD

Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

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

Study arms

  • Experimental
    Segmental Breathing Exercises

    Patients receive segmental breathing exercises after open heart surgery to improve lung expansion and cardiopulmonary function

    Behavioral: Segmental Breathing Exercises

  • Experimental
    Active Cycle Breathing Technique

    Patients receive active cycle breathing technique (ACBT) after open heart surgery to enhance airway clearance and improve respiratory function.

    Behavioral: Active Cycle Breathing Technique

  • Active comparator
    Standard Postoperative Care

    Patients receive routine postoperative care without structured breathing exercise interventions.

    Other: Standard postoperative care

Interventions

  • BehavioralSegmental Breathing Exercises

    Deep breathing exercises focusing on specific lung segments to improve ventilation, lung expansion, and oxygenation in post open heart surgery patients.

  • BehavioralActive Cycle Breathing Technique

    A combination of breathing control, thoracic expansion exercises, and forced expiration technique to improve airway clearance and lung function.

  • OtherStandard postoperative care

    Participants will receive routine postoperative care according to institutional protocols following cardiac surgery. This includes standard medical and nursing management such as oxygen therapy, pain control, monitoring of vital signs, and mobilization as tolerated, without additional structured respiratory physiotherapy interventions.

06

What researchers measure

Primary outcomes

  1. Oxygen Saturation (SpO₂)

    Assessment of peripheral oxygen saturation in patients after open heart surgery undergoing breathing exercises (segmental breathing exercises or active cycle breathing technique)

    Time frame: Measurements will be obtained at baseline pre-intervention, 1 hour post-intervention, and 6 hours post-intervention during hospital stay

  2. Respiratory Rate

    Assessment of respiratory rate in patients after open heart surgery undergoing breathing exercises.

    Time frame: Measurements will be obtained at baseline pre-intervention,1 hour post-intervention, and 6 hours post-intervention

  3. Heart Rate

    Assessment of heart rate in patients after open heart surgery undergoing breathing exercises.

    Time frame: Measurements will be obtained at baseline pre-intervention, 1 hour post-intervention, and 6 hours post-intervention during hospital stay

  4. Systolic Blood Pressure, Diastolic Blood Pressure, and Pulse Pressure

    Assessment of Systolic Blood Pressure Pulse Pressure, and Diastolic Blood Pressure in patients after open heart surgery undergoing breathing exercises.

    Time frame: Measurements will be obtained at baseline pre-intervention, 1 hour post-intervention, and 6 hours post-intervention during hospital stay

Secondary outcomes

  1. Dyspnea Index

    Assessment of dyspnea index in patients after open heart surgery using a standardized dyspnea scale contain ten questions for score 0 = Never. 1 = Almost never. 2 = Sometimes. 3 = Almost always. 4 = Always , the higher number is the worst that to evaluate changes before interventions and after implementation of segmental breathing exercises or active cycle breathing techniques.

    Time frame: measur at baseline pre-intervention and post-intervention after 6 hours.

Other outcomes

  1. Mean Arterial Pressure

    Assessment of Mean Arterial Pressure in patients after open heart surgery undergoing breathing exercises.

    Time frame: Measurements will be obtained at baseline pre-intervention, 1 hour post-intervention, and 6 hours post-intervention during hospital stay

07

Study locations

3 of 3 sites recruiting
  • Ibn Al-Bitar Specialized Hospital for Cardiac Surgery
    Baghdad, Baghdad Governorate 10001, Iraq
    Recruiting
    • Muslim Aqeel Essa, Master student · Principal investigator
  • Iraqi Center for Heart Diseases
    Baghdad, Baghdad Governorate 10001, Iraq
    Recruiting
    • Muslim Aqeel Essa, Master student · Principal investigator
  • Al-Hassan Al-Mujtaba Hospital
    Karbala, Kerbala Governorate 56001, Iraq
    Recruiting
    • Muslim Aqeel Essa, Master student · Principal investigator
08

References and documents

Publications

  • Salehi Derakhtanjani A, Ansari Jaberi A, Haydari S, Negahban Bonabi T. Comparison the Effect of Active Cyclic Breathing Technique and Routine Chest Physiotherapy on Pain and Respiratory Parameters After Coronary Artery Graft Surgery: A Randomized Clinical Trial. Anesth Pain Med. 2019 Oct 16;9(5):e94654. doi: 10.5812/aapm.94654. eCollection 2019 Oct. PubMed 31903332 ↗

Individual participant data

Plan to share: No — IPD will not be shared due to patient privacy and confidentiality concerns.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jan 2026 (actual). Primary completion is estimated for Jul 2026, 6 months after the start.

Of 266 non-industry interventional studies with no phase under Dyspnea, half reached primary completion within 13 months of starting (the median), counting those still running; a quarter within 6 and three quarters within 28. This study's planned 6 months is below that.

Counting every sponsor, half of 282 studies reached it within 13 months; a quarter within 6 and three quarters within 28.

How these figures are worked out, and which studies are left out of them.

Registered
May 7, 2026
First posted
May 18, 2026
StartActual
Jan 2, 2026
Primary completionEst.
Jul 10, 2026
CompletionEst.
Oct 10, 2026
Last update
May 18, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07591987
Responsible party
Muslim Aqeel Essa (Principal Investigator, University of Baghdad) — Principal investigator
First posted
May 18, 2026
Start date
Jan 2, 2026
Primary completion
Jul 10, 2026 (estimated)
Completion
Oct 10, 2026 (estimated)
Last update
May 18, 2026

Study contacts

Muslim Aqeel Essa, Master Student
Contact
muslim.eesa2402m@conursing.uobaghdad.edu.iq
+9647822218483
Rusul Khalid Kadhim, Master Student
Contact
Wafaa Abd Ali Hattab, Assist prof
principal investigator · College of Nursing , University of Baghdad

Oversight

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

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