Effects of early mobility on recovery in cardiac ICU patients
Effects of Early Mobilization on Functional Capacity, Physical Activity and Kinesiophobia in Post Coronary Artery Bypass Grafting
This study tests whether getting patients moving early after heart surgery helps them recover better and faster in the ICU.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 70 (estimated) |
| Ages | 40 Years to 70 Years |
| Sex | All |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Peshawar, KPK) |
| Trial ID | NCT06029556 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of different early mobility protocols on post-operative recovery in patients who have undergone coronary artery bypass grafting (CABG). It aims to compare the effectiveness of mobility out of bed and ergometry in bed on various outcomes such as functional capacity, ICU mortality, and length of hospital stay. By assessing these protocols, the study seeks to identify the best approach to enhance recovery in cardiac ICU settings.
Who should consider this trial
Good fit: Ideal candidates for this study are vitally stable patients aged 40-70 who have undergone their first elective CABG and are extubated without complications.
Not a fit: Patients with post-anesthesia psychosis, physical disabilities, or those who have experienced a post-CABG stroke may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved recovery outcomes and reduced hospital stays for post-CABG patients.
How similar studies have performed: Other studies have shown promising results with early mobility protocols in ICU settings, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 40-70 years * Both Genders * Extubated patients with no Complication * Post CABG (Elective) * Vitally stable * 1st CABG * Selective CABG surgeries Exclusion Criteria: * Post anesthesia Psychosis * Corrective surgeries * Post CABG Stroke * Infectious wound * Participants with a physical disability * Intra-aortic balloon pump (IABP)
Where this trial is running
Peshawar, KPK
- Rehman Medical Institute — Peshawar, Kpk, Pakistan (Recruiting)
Study contacts
- Principal investigator: Sumaiyah Obaid, MS — Riphah International University
- Study coordinator: Sumaiyah Obaid, MS
- Email: sumaiyah.obaid@riphah.edu.pk
- Phone: +923212683462
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.