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N/A N=54 Randomized Supportive Care

Transitional Rehabilitation in CABG Patients

Coronary Artery Disease · Coronary Artery Bypass Graft Surgery

Enrolled (actual)
54
Serious AEs
0.0%
Results posted
Aug 2021
Primary outcome: Primary: Short Physical Performance Battery — 7.33; 8.00; 11.44; 10.90 units on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
neuromuscular electrical stimulation (Device)
Age
Adult, Older Adult · 50+ yrs
Sex
All
Sponsor
University of Vermont
Primary completion
Oct 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Short Physical Performance Battery
7.33; 8.00; 11.44; 10.90
SECONDARY
6 Minute Walk Distance
216; 238; 482; 431
SECONDARY
Medical Outcomes Short Form 36 - Physical Function
40; 33; 70; 58
SECONDARY
Medical Outcome Short Form 36 - Role Physical
26; 21; 19; 18
SECONDARY
Medical Outcomes Short Form 36 - Bodily Pain
31; 28; 28; 27
SECONDARY
Medical Outcomes Short Form 36 - General Health
71; 63; 81; 72
SECONDARY
Medical Outcomes Short Form 36 - Vitality
55; 53; 55; 51
SECONDARY
Medical Outcomes Short Form 36 - Social Function
74; 63; 76; 72
SECONDARY
Medical Outcomes Short Form 36 - Role Emotional
65; 54; 72; 51
SECONDARY
Medical Outcomes Short Form 36
77; 74; 86; 78
SECONDARY
Physical Activity
125.6; 109.6

Summary

The goal of this research study is to understand whether an at-home exercise program started soon after CABG surgery, and continuing for 4 weeks following discharge from the hospital, can preserve or improve physical function.

Eligibility Criteria

Inclusion Criteria

  • 50-80 yrs of age
  • ambulatory
  • scheduled for coronary artery bypass graft surgery
  • able to provide informed consent

Exclusion Criteria

  • rheumatoid arthritis or other inflammatory/autoimmune disease
  • cancer, excluding non-melanoma skin cancer
  • exercise limiting peripheral vascular disease
  • neuromuscular disease or neuromuscular dysfunction associated with cerebrovascular event
  • body mass index >38 kg/m2
  • valvular heart disease not corrected surgically
  • lower extremity blood clot or implantable cardioverter-defibrillator
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03892460). 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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