Skip to content

Effects of Functional Electrical Stimulation in Patients Undergoing Coronary Artery Bypass Grafting Surgery

Effects of Functional Electrical Stimulation in Patients Undergoing Coronary Artery Bypass Grafting Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03560713
Enrollment
25
Registered
2018-06-18
Start date
2017-07-01
Completion date
2020-03-10
Last updated
2020-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Muscle Wasting

Brief summary

Even with major advances in clinical therapy and percutaneous interventions, coronary artery bypass grafting (CABG) is the most common cardiac surgery performed worldwide and is an effective treatment in reducing symptoms and mortality in patients with coronary artery disease (CAD). However, CABG is a complex procedure that triggers a series of clinical and functional complications, such as series postoperative repercussions as muscle wasting in the first four hours after surgery. For quantification of changes in muscle structure and morphology ultrasonography has been used. In this context, cardiac rehabilitation program (CRP) is an essential component of care in CABG patients, because this intervention can prevent muscle weakness and wasting. Among different treatment modalities, functional electrical stimulation (FES) is a feasible therapy for neuromuscular activation and prevent muscle weakness and wasting in patients in phase I CRP, however the effect of this intervention in phase II CRP not been fully elucidated. The purpose of this study will to assess the effects of FES plus combined aerobic and resistance training on muscle thickness of quadriceps femoris, lower limbs muscle strength, functional capacity, QoL in in CABG patients enrolled in a phase II CR program.

Interventions

Participants will perform 12 weeks of FES (Neurodyn High Volt, IBRAMED, São Paulo/SP, Brasil), three times a week, frequency 25Hz, pulse rate of 200μs, ON:OFF 5:5, individual maximum tolerated intensity; minimum at strong but comfortable visible muscle contraction (without causing undue pain or discomfort to the participant). during 30 minutes nd receive aerobic exercise training and resistance exercises for upper limbs and lower limbs.

OTHERFunctional Electrical Stimulation (FES) sham

Participants will perform 12 weeks of Functional Electrical Stimulation (FES) sham (Neurodyn High Volt, IBRAMED, São Paulo/SP, Brasil), three times a week, frequency 5Hz, pulse rate of 200μs, ON:OFF 5:5, without muscle contraction during 30 minutes nd receive aerobic exercise training and resistance exercises for upper limbs and lower limbs.

Sponsors

Universidade Federal de Santa Maria
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
55 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Patients undergoing CABG up to three weeks before the initiation of the study, a clinical course without complications during hospitalization * Clinically stable * The absence of smoking (previous or current).

Exclusion criteria

* Unstable angina * Myocardial infarction and heart surgery up to three months before the survey * Chronic respiratory diseases * Hemodynamic instability * Orthopedic and neurological diseases that may preclude the achievement of the cardiopulmonary test and Cardiac Rehabilitation exercises * Psychological and/or cognitive impairment that restrict them to respond to questionnaires * Changes of skin sensitivity,skin lesion and allergic skin problems * Severe lymphedema * Uncontrolled diabetes mellitus * Acute superficial venous thrombophlebitis * Systemic arterial hypertension

Design outcomes

Primary

MeasureTime frameDescription
Muscle thickness of the quadriceps femorisChange in muscle thickness (in cm) from baseline at after 12 weeks of rehabilitation cardiac admission, an average of 3 monthsMuscle thickness of the quadriceps femoris will be assessed by ultrasonography (baseline and after 12 weeks)

Secondary

MeasureTime frameDescription
Rectus femoris cross-sectional areaChange in rectus femoris cross-sectional area (in cm2) from baseline at after 12 weeks of rehabilitation cardiac admission, an average of 3 monthsRectus femoris cross-sectional area will be assessed by ultrasonography
Rectus femoris and vastus intermedius thicknessChange in rectus femoris and vastus intermedius thickness (in cm) from baseline at after 12 weeks of rehabilitation cardiac admission, an average of 3 monthsRectus femoris and vastus intermedius thickness will be assessed by ultrasonography
Ankle-brachial indexChange in ankle-brachial index (in mmHg) from baseline at after 12 weeks of rehabilitation cardiac admission, an average of 3 monthsAnkle-brachial index will be assessed by by Doppler ultrasonography using color Doppler.
Vastus intermedius, rectus femoris echo intensityChange in vastus intermedius and rectus femoris echo intensity (in region of interest -ROI) from baseline at after 12 weeks of rehabilitation cardiac admission, an average of 3 monthsVastus intermedius, rectus femoris echo intensity will be assessed by ultrasonography (baseline and after 12 weeks)
Quality of lifeChange in MacNew scores from baseline at after 12 weeks of rehabilitation cardiac admission, an average of 3 monthsQuality of life will be measured by a MacNew Heart Disease health-related quality of life instrument
Lower-limb functional exercise capacityChange in distance walked (meters) by the patients during six-minute walk test from baseline at after 12 weeks of rehabilitation cardiac admission, an average of 3 monthsLower-limb functional exercise capacity will be assessed by six-minute walk test
Peripheral muscle strength of the lower limbsChange in peripheral muscle strength (in number of repetitions performed in the STST) from baseline at after 12 weeks of rehabilitation cardiac admission, an average of 3 monthsPeripheral muscle strength of the lower limbs will be measured by sit-to-stand test (STST).

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026