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NCT Number: NCT07724353

Early Cardiopulmonary Rehabilitation Bundle 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)

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Key information

Conditions

Cardiac Surgeries

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Assiut University Heart Hospital , Assiut University Hospital

Asyut, 71515, Egypt

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patient aged 18-65 years
  • patient hemodynamically stable postoperative
  • patient voluntarily participates in study

Exclusion criteria

  • re-operative cardiac surgery
  • patients with arrhythmia in operation room
  • non elective cardiac surgery
  • EURO categories 3 and 4

Treatment and study plan

Early cardiopulmonary rehabilitation bundle

Other

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)

Primary outcomes

  1. 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

  2. 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

Secondary outcomes

  1. patient psychological status in ICU postoperative

    Time frame: From study enrollment up t o7 days after surgery

    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

Study contacts

Contact information is provided by the study sponsor or research team.

Taha HM Ibrahim, MSc

CONTACT

[email protected]

201091084749

mona AM Mohamed, PhD

CONTACT

2012261644645

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Official study title

Early Cardiopulmonary Rehabilitation Bundle: Its' Effect On Functional Capacity and Outcomes of Cardiac Surgeries Patients

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jul 24, 2026
Registry last updated
Jul 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.