An interventional study of Early cardiopulmonary rehabilitation bundle in Cardiac Surgeries, sponsored by Assiut University. Not yet recruiting at 1 site in Egypt. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-24.
Sponsored by Assiut University · Not applicable, Interventional, and Supportive care
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)
Assiut University is the lead sponsor of 4,901 studies on the registry; 2,098 are open to participants now.
Of its 13 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
study group Early cardiopulmonary rehabilitation will be apply on study group for improving functional capacity and reducing negative outcome postoperatively
Other: Early cardiopulmonary rehabilitation bundle
control group will receive the routine postoperative ICU rehabilitation care
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)
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
Time frame: 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
Time frame: From study enrollment up t o7 days after surgery
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
Time frame: From study enrollment up t o7 days after surgery
Plan to share: No
No publications or documents are linked to this record.
This study is not yet recruiting, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
Assiut University