Trials / Completed
CompletedNCT03892460
Transitional Rehabilitation in CABG Patients
Novel Transitional Rehabilitation Care in Coronary Artery Bypass Graft (CABG) Patients
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 54 (actual)
- Sponsor
- University of Vermont · Academic / Other
- Sex
- All
- Age
- 50 Years – 80 Years
- Healthy volunteers
- Not accepted
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.
Detailed description
Coronary artery bypass graft (CABG) surgery is a common surgical procedures and an important treatment option for coronary artery disease. The post-surgery period of rest and recovery is associated with cardiorespiratory and skeletal muscle deconditioning. 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 serve as a bridge between surgery and the start of cardiac rehabilitation to preserve or improve physical function. Volunteers will be randomly assigned to receive neuromuscular electrical stimulation (NMES) of their quadriceps muscles or not to receive NMES (control group). Volunteers will be evaluated prior to CABG, upon discharge and 4 weeks Post-CABG surgery. Assessments will include measurements of physical function by the Short Physical Performance Battery, 6 min walk tests and body composition analysis, as well as assessment of subjective physical functional capacity and quality of life using the Medical Outcomes Short form 36. Additionally, accelerometry will be used to monitor weight-bearing physical activity during the 4 week treatment phase.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | neuromuscular electrical stimulation | bilateral quadriceps exercise with neuromuscular electrical stimulation |
Timeline
- Start date
- 2017-09-01
- Primary completion
- 2019-10-24
- Completion
- 2019-10-24
- First posted
- 2019-03-27
- Last updated
- 2021-08-03
- Results posted
- 2021-08-03
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03892460. Inclusion in this directory is not an endorsement.