Clinical trial Recruiting at 1 site Interventional Ages 40 to 55

Early cardiac rehabilitation after mitral or aortic valve replacement

Official title: Phase One Cardiac Rehabilitation Outcomes Post Valve Replacement Surgery

Run by South Valley University · NCT07205393 · Data updated 2026-11-12

This study tests whether a supervised early cardiac rehabilitation program helps adults aged 40–60 recover heart and lung function and walking ability after mitral or aortic valve replacement.

More Transcatheter Aortic Valve Replacement trials

Quick facts

Study typeInterventional
Ages40 Years to 55 Years
SexAll
Enrollment60 (estimated)
SponsorSouth Valley University
Academic / other
Locations1 site (Qina)
StatusRecruiting
StartedJanuary 1, 2025
Main results expectedOctober 1, 2025
Study endsOctober 20, 2025
Registry record updatedOctober 3, 2025
Trial IDNCT07205393 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are hemodynamically stable adults aged 40–60 who had elective mitral or aortic valve replacement, can understand and complete measurements, and can provide written informed consent.

Probably not a fit

Patients with prior ischemic heart disease, severe musculoskeletal disorders, persistent or paroxysmal atrial fibrillation, severe heart failure, uncontrolled arrhythmias, other comorbidities limiting physical activity, or those who had emergency surgery are unlikely to benefit or be eligible.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

In Qena, Egypt, 60 patients aged 40–60 who underwent elective mitral or aortic valve replacement were randomized to a phase one cardiac rehabilitation program or routine postoperative physical therapy. The rehabilitation group received supervised physical exercises and respiratory training while the control group received standard clinic care. Outcomes included oxygen saturation, spirometry measures, and the six-minute walk test, all measured before and after six consecutive weeks of the assigned program. The trial focused on short-term changes in cardiovascular function, pulmonary capacity, and functional ability.

Why it matters

Potential benefit: If successful, the program could speed recovery and improve cardiovascular and pulmonary function, functional capacity, and quality of life after valve replacement.

How similar studies have gone: Similar cardiac rehabilitation programs have demonstrated benefits after cardiac surgery, although evidence specifically for phase one rehab after valve replacement is more limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* The inclusion criteria was elective mitral or aortic valve replacement
* and to be hemodynamically stable to qualify for a structured rehabilitation program.
* Being able to understand and complete measurements.
* And provide informed written consent.

Exclusion Criteria:

* Patient with ischemic heart disease before surgery.
* Those with severe musculoskeletal system disorders.
* Patients who had persistent or paroxysmal atrial fibrillation.
* Individuals with severe heart failure.
* uncontrolled arrhythmias.
* Comorbidity complicating physical activity or other contraindications to phase one cardiac rehabilitation and Patients who underwent an emergency surgical intervention.

Where it's running

  • South valley university
    Qina, Egypt
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.