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N/A N=1,024 Prevention

Effect of an Educational Intervention on Cardiac Patients' Participation Rate in Cardiac Rehabilitation Programs

Coronary Artery Disease

Enrolled (actual)
1,024
Serious AEs
26.6%
Results posted
Mar 2012
Primary outcome: Primary: Number of Patients Participating in Cardiac Rehabilitation Programs (CRPs)1-year Post Coronary Artery Bypass Grafting (CABG)Surgery in the Intervention and Control Groups — 156; 86 participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Increasing awareness to cardiac rehabilitation programs (Behavioral)
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
Sheba Medical Center
Primary completion
Jun 2009

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Patients Participating in Cardiac Rehabilitation Programs (CRPs)1-year Post Coronary Artery Bypass Grafting (CABG)Surgery in the Intervention and Control Groups
156; 86
SECONDARY
MacNew Heart Disease Health Related Quality of Life (HRQL) Scale. A Self-administered Heart Disease-specific Health-related Quality of Life (HRQL) Instrument.
5.58; 5.27

Summary

The main aim of the study is to determine the effectiveness of an educational intervention designed to increase attendance of coronary artery bypass grafting (CABG) patients at Cardiac Rehabilitation Programs (CRPs) on actual CRP participation rate and; examine patient-related factors (demographic, health, psychosocial, awareness) influencing patients' attendance at CRPs. We hypothesized that the proportion of CABG patients participating in CRPs will increase significantly to 20-30% following the educational intervention employed.

Eligibility Criteria

Inclusion Criteria

  • Patients undergoing Coronary Artery Bypass Grafting with or without valve replacement

Exclusion Criteria

  • Institutionalized patients
  • Patients with severe co-morbidities for whom cardiac rehabilitation (CR) is contra-indicated
  • Patients who sustained a severe surgical complication preventing them from participating in CR (general stroke with severe disability)
  • Patients residing farther than 30 km from a rehabilitation center
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00356863). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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