Menu
Not yet recruiting NCT07724353

Early Cardiopulmonary Rehabilitation Bundle Functional Capacity and Outcomes of Cardiac Surgeries Patients

No phase Interventional Cardiac Surgeries

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Early cardiopulmonary rehabilitation bundle.
Who it may be relevant to
Registry conditions: Cardiac Surgeries. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

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

Overview

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)

Interventions

  • Other Early cardiopulmonary rehabilitation bundle
    The 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)

Primary outcome measures

  • physical activity [Time frame: From study enrollment up t o7 days after surgery]
  • complications [Time frame: From study enrollment up t o7 days after surgery]
Secondary outcome measures (1)
  • patient psychological status in ICU postoperative [Time frame: From study enrollment up t o7 days after surgery]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Supportive care

Study locations

Egypt · 1 center
  • Assiut University Heart Hospital , Assiut University Hospital — Asyut

Identifiers

NCT: NCT07724353 · 1120261460

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗