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DyspneaNCT07591987

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

A study testing Segmental Breathing Exercises, Active Cycle Breathing Technique and Standard postoperative care in people with Dyspnea and Cardiopulmonary Dysfunction, run by University of Baghdad at 3 sites in Iraq.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 75 years
What is being tested?
Segmental Breathing Exercises, Active Cycle Breathing Technique and Standard postoperative care
Could I receive a placebo?
No, everyone receives an active treatment
How many people
99 participants
Where
3 sitesIraq
Study dates
2 Jan 2026to 10 Oct 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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.

Who cannot join

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

Trial locations and contacts

3 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Muslim Aqeel Essa, Master Student contact

+9647822218483

muslim.eesa2402m@conursing.uobaghdad.edu.iq

Rusul Khalid Kadhim, Master Student contact

Iraq3 sites, 3 recruiting
  • Ibn Al-Bitar Specialized Hospital for Cardiac Surgery

    Baghdad, Baghdad Governorate, 10001

    Muslim Aqeel Essa, Master student

    Recruiting
  • Iraqi Center for Heart Diseases

    Baghdad, Baghdad Governorate, 10001

    Muslim Aqeel Essa, Master student

    Recruiting
  • Al-Hassan Al-Mujtaba Hospital

    Karbala, Kerbala Governorate, 56001

    Muslim Aqeel Essa, Master student

    Recruiting

Other trials in Iraq

About this study

Official title: Effect of Segmental Breathing Versus Active Cycle Breathing Techniques on Dyspnea and Cardiopulmonary Parameters Among Patients After Open Heart Surgery: Randomized Controlled Trial.

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.

Read more

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.

Being tested
Segmental Breathing Exercises, Active Cycle Breathing Technique, Standard postoperative care
Keywords
Open Heart Surgery, Cardiac Surgery, Breathing Exercises, Segmental Breathing Exercises, Active Cycle Breathing Technique, Postoperative Patients, Adult Patients, Dyspnea, Cardiopulmonary Parameters
Medical subject headings
Dyspnea, Coronary Artery Disease

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Segmental Breathing ExercisesBehavioural

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

  • Active Cycle Breathing TechniqueBehavioural

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

  • Standard postoperative careOther

    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.

Study groups in NCT07591987
Study groupRoleWhat they receive
Segmental Breathing ExercisesExperimentalPatients receive segmental breathing exercises after open heart surgery to improve lung expansion and cardiopulmonary function
Receives: Behavioral: Segmental Breathing Exercises
Active Cycle Breathing TechniqueExperimentalPatients receive active cycle breathing technique (ACBT) after open heart surgery to enhance airway clearance and improve respiratory function.
Receives: Behavioral: Active Cycle Breathing Technique
Standard Postoperative CareActive comparatorPatients receive routine postoperative care without structured breathing exercise interventions.
Receives: Other: Standard postoperative care

What is being measured

The primary outcome is the main question the study is designed to answer.

  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)

    Measured: 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.

    Measured: 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.

    Measured: 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.

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

Secondary outcomes (1)
  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.

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

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 May 2026
  2. Study start2 Jan 2026
  3. Primary completion10 Jul 2026 (estimated)
  4. Study completion10 Oct 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
participants will be randomly assigned into intervention groups receiving segmental breathing exercises and another receiving active cycle breathing techniques compare to control group after open heart surgery to evaluate their effects on dyspnea and cardiopulmonary parameters.
Masking
Single blind
Who is masked
Participant
Enrolment
99 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07591987
Sponsor's protocol ID
UOB-NUR-2026-03
Status last verified
May 2026
First submitted
7 May 2026
Last updated
18 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: IPD will not be shared due to patient privacy and confidentiality concerns.

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

Questions about this trial

What is this clinical trial studying?

A study testing Segmental Breathing Exercises, Active Cycle Breathing Technique and Standard postoperative care in people with Dyspnea and Cardiopulmonary Dysfunction, run by University of Baghdad at 3 sites in Iraq.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 18 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in Iraq. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Muslim Aqeel Essa, Master Student (+9647822218483, muslim.eesa2402m@conursing.uobaghdad.edu.iq), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Oxygen Saturation (SpO₂) (time frame: Measurements will be obtained at baseline pre-intervention, 1 hour post-intervention, and 6 hours post-intervention during hospital stay). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07591987, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 May 2026.

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