Cardiac SurgeriesNCT07724353
Early Cardiopulmonary Rehabilitation Bundle Functional Capacity and Outcomes of Cardiac Surgeries Patients
A study testing Early cardiopulmonary rehabilitation bundle in people with Cardiac Surgeries, run by Assiut University at 1 site in Egypt.
Trial summary
The goal of this quasi-experimental study is to evaluate the impact of Early. Cardiopulmonary Rehabilitation Bundle on Functional Capacity and Outcomes in Cardiac Surgeries Patients The main question is Patients receive early cardiopulmonary rehabilitation bundle will. Read more about this study
- Who is it for?
- Ages 18 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- Cardiac Surgeries
- What is being tested?
- Early cardiopulmonary rehabilitation bundle
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 140 participants
- Where
- 1 siteEgypt
- Study dates
- 20 Jul 2026to 20 Mar 2027
- 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 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- patient aged 18-65 years
- patient hemodynamically stable postoperative
- patient voluntarily participates in study
Who cannot join
- re-operative cardiac surgery
- patients with arrhythmia in operation room
- non elective cardiac surgery
- EURO categories 3 and 4
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
mona AM Mohamed, PhD contact
Egypt1 site, 1 recruiting
- Recruiting
Assiut University Heart Hospital , Assiut University Hospital
Asyut, 71515
About this study
Official title: Early Cardiopulmonary Rehabilitation Bundle: Its' Effect On Functional Capacity and Outcomes of Cardiac Surgeries Patients
The goal of this quasi-experimental study is to evaluate the impact of Early. Cardiopulmonary Rehabilitation Bundle on Functional Capacity and Outcomes in Cardiac Surgeries Patients The main question is Patients receive early cardiopulmonary rehabilitation bundle will.
affect or not functional capacity and not decrease negative outcomes. postoperative? Researchers will compare the effect on 140 patients divided into 2. groups (70 patients in study group and 70 patients in control group)
- Conditions
- Cardiac Surgeries
- Being tested
- Early cardiopulmonary rehabilitation bundle
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Early cardiopulmonary rehabilitation bundleOther
The bundle include all of following :
- pulmonary rehabilitation by using (Inspiratory muscle training and Active cycle of breathing techniques)
- cardiac rehabilitation by using (Early mobilization and Ergometric bed cycle)
| Study group | Role | What they receive |
|---|---|---|
| cardiopulmonary rehabilitation | Active comparator | study group Early cardiopulmonary rehabilitation will be apply on study group for improving functional capacity and reducing negative outcome postoperatively Receives: Other: Early cardiopulmonary rehabilitation bundle |
| routine rehabilitation | Placebo comparator | control group will receive the routine postoperative ICU rehabilitation care Receives: Other: Early cardiopulmonary rehabilitation bundle |
What is being measured
The primary outcome is the main question the study is designed to answer.
physical activity
evaluate the impact of Early Cardiopulmonary Rehabilitation Bundle on physical activity Postoperatively will be assess by using Functional exercise capacity tool which is assess the level of patients physical exertion postoperatively
Measured: From study enrollment up t o7 days after surgery
complications
evaluate the impact of Early Cardiopulmonary Rehabilitation Bundle occurrence of complications postoperative will be assess by using patient outcomes tool
Measured: From study enrollment up t o7 days after surgery
Secondary outcomes (1)
patient psychological status in ICU postoperative
the outcome will be assess by using Quality of life questionnaire which is screening tool for depressive symptoms. Scores of 5-9, 10-14, 15-19, and ≥20 indicate mild, moderate, moderately severe, and severe depression
Measured: From study enrollment up t o7 days after surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Jul 2026
- Study start20 Jul 2026
- Primary completion20 Feb 2027 (estimated)
- Study completion20 Mar 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cardiac SurgeriesStudies of the same condition, open and under way.
- More trials run by Assiut UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Supportive care
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 140 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Assiut University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Taha Hussein Mohamed, Assiut University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07724353
- Sponsor's protocol ID
- 1120261460
- Status last verified
- Oct 2026
- First submitted
- 10 Jul 2026
- Last updated
- 28 Oct 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 28 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Early Cardiopulmonary Rehabilitation Bundle: Its' Effect On Functional Capacity and Outcomes of Cardiac Surgeries Patients
- ClinicalTrials.gov ID
- NCT07724353
- Acronym / sponsor ID
- 1120261460
- Conditions
- Cardiac Surgeries
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 140 participants (estimated)
- Lead sponsor
- Assiut UniversityUniversity, hospital or other
- Study start
- 20 Jul 2026 (actual)
- Primary completion
- 20 Feb 2027 (estimated)
- Study completion
- 20 Mar 2027 (estimated)
- First posted
- 24 Jul 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this quasi-experimental study is to evaluate the impact of Early. Cardiopulmonary Rehabilitation Bundle on Functional Capacity and Outcomes in Cardiac Surgeries Patients The main question is Patients receive early cardiopulmonary rehabilitation bundle will.
affect or not functional capacity and not decrease negative outcomes. postoperative? Researchers will compare the effect on 140 patients divided into 2. groups (70 patients in study group and 70 patients in control group)
Study design
- Primary purpose
- Supportive care
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| cardiopulmonary rehabilitation | Active comparator | Other: Early cardiopulmonary rehabilitation bundlestudy group Early cardiopulmonary rehabilitation will be apply on study group for improving functional capacity and reducing negative outcome postoperatively |
| routine rehabilitation | Placebo comparator | Other: Early cardiopulmonary rehabilitation bundlecontrol group will receive the routine postoperative ICU rehabilitation care |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- patient aged 18-65 years
- patient hemodynamically stable postoperative
- patient voluntarily participates in study
Key exclusion criteria (4 listed)
- re-operative cardiac surgery
- patients with arrhythmia in operation room
- non elective cardiac surgery
- EURO categories 3 and 4
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Early cardiopulmonary rehabilitation bundleThe bundle include all of following : 1. pulmonary rehabilitation by using (Inspiratory muscle training and Active cycle of breathing techniques) 2. cardiac rehabilitation by using (Early mobilization and Ergometric bed cycle) | Other | cardiopulmonary rehabilitation, routine rehabilitation |
Primary outcome
physical activity
Time frame: From study enrollment up t o7 days after surgery
evaluate the impact of Early Cardiopulmonary Rehabilitation Bundle on physical activity Postoperatively will be assess by using Functional exercise capacity tool which is assess the level of patients physical exertion postoperatively
complications
Time frame: From study enrollment up t o7 days after surgery
evaluate the impact of Early Cardiopulmonary Rehabilitation Bundle occurrence of complications postoperative will be assess by using patient outcomes tool
1 secondary outcome
patient psychological status in ICU postoperative
Time frame: From study enrollment up t o7 days after surgery
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Oct 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
mona AM Mohamed, PhD contact
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Early cardiopulmonary rehabilitation bundle in people with Cardiac Surgeries, run by Assiut University at 1 site in Egypt.
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 3 inclusion and 4 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 28 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Egypt. 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. Some participants in this study may receive a placebo. 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 Taha HM Ibrahim, MSc (201091084749, tahahussien@nursing.aun.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
physical activity (time frame: From study enrollment up t o7 days after surgery). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 28 Oct 2026.