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Eccentric Manual Resistance Training in Patients With Ischemic CMP

Eccentric Manual Resistance Training for Improvement of Strength and Function in Patients With Ischemic Cardiomyopathy and Mildly Reduced Ejection Fraction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04829955
Enrollment
16
Registered
2021-04-02
Start date
2022-06-29
Completion date
2023-12-12
Last updated
2024-05-01

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

Conditions

Ischemic Cardiomyopathy

Keywords

Eccentric training, Ischemic Cardiomyopathy, Concentric training

Brief summary

Patients with ischemic cardiomyopathy and mildly reduced ejection fraction suffer from reduced functional capacity and fatigue caused by loss of muscle strength and reduced aerobic capacity. A few studies have shown that structured endurance and resistance training programs were able to improve walking capacity and limb strength. Although both concentric and eccentric training programs are beneficial for these patients, eccentric training is less stressful to the cardiovascular system. The aim of the study is to determine if eccentric-orientated body weight and manual resistance training in ischemic cardiomyopathy patients will lead to superior results compared to concentric training.

Detailed description

BACKGROUND: Eccentric resistance training demonstrated positive effects in ischemic cardiomyopathy patients in several studies. These studies were mainly set on device-based training interventions comparing eccentric-orientated and concentric-orientated training. Eccentric-orientated training induced comparable positive effects on cardiac and functional levels and even better effects on muscle strength improvement. RESEARCH AIMS: The aim of the study is to determine if eccentric-orientated body weight and manual resistance training in ischemic cardiomyopathy patients will allow a more significant improvement in maximum voluntary contraction force of the knee extensors compared to concentric training. In contrast to previous studies, these interventions will be set without use of training devices. In addition, changes in the muscle cross section of the quadriceps muscle will be calculated by skeletal muscle ultrasound. Functional changes and quality of life will be assessed using one minute sit to stand test, six minutes walking test and Kansas City Cardiomyopathy Questionnaire. Cardiac outcome parameters will be assessed by using body composition and hemodynamic parameters as well as echocardiography, laboratory values and specific biomarkers for sarcopenia / cachexia. METHODS: The investigators propose to run a monocentric, prospective, double arm, open, randomized controlled trial. Eccentric-orientated training will be delivered to 30 ischemic cardiomyopathy patients. These patients will be randomized into two groups at the beginning, followed by a 6-weeks observation phase (without intervention for internal quality control of the measurement parameters). The intervention-phase will consist of six weeks of three times weekly either eccentric or concentric-oriented training. Outcome measurements will take place after randomization, after 6 weeks of observation as well as after the intervention phase

Interventions

OTHEREccentric manual resistance training

Eccentric bodyweight resistance training

OTHERConcentric manual resistance resistance training

Concentric bodyweight resistance training

Sponsors

Vienna Hospital Association
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
45 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Male / female, 45-85a * Ischemic cardiomyopathy with mildly reduced ejection fraction (40 -50%) * Coronary heart disease

Exclusion criteria

* Acute coronary syndrome, myocarditis or pericarditis in the last 3 months * Cardiac decompensation in the last 3 months * Severe symptomatic heart failure NYHA IV (New York Heart Association) * Device - carrier (ICD= Intracardial Defibrillator, CRT= Cardiac Resynchronization Therapy, PM=Pacemaker) * Hemodynamically significant valvular disease * Symptomatic cardiac arrhythmia * Intractable, uncontrolled hypertension (repetitive blood pressure \> 150/100) * Severe comorbidities, which lead to study exclusion by the investigator * Pregnancy / nursing

Design outcomes

Primary

MeasureTime frameDescription
MVC of knee-extensors isometricBaselineKnee dynamometer

Secondary

MeasureTime frameDescription
Muscle cross section area of the quadriceps femoris muscle calculated by skeletal muscle ultrasound measurementBaselineSonographic measurement
Six- minutes walking test (6MWT)BaselineMeasures the walking distance within 6 minutes.
One-minute sit to stand testBaselineMeasures sit to stand repetitions within one minute.
Quality of life (QoL)BaselineKansas City Cardiomyopathy questionnaire (KCCQ) In the KCCQ, an overall summary score can be derived from the physical function, symptom (frequency and severity), social function and quality of life domains. For each domain, the validity, reproducibility, responsiveness and interpretability have been independently established. Scores are transformed to a range of 0-100, in which higher scores reflect better health status.
Quality of life (QoL): questionnaireAfter 6 weeks of trainingKansas City Cardiomyopathy questionnaire (KCCQ) In the KCCQ, an overall summary score can be derived from the physical function, symptom (frequency and severity), social function and quality of life domains. For each domain, the validity, reproducibility, responsiveness and interpretability have been independently established. Scores are transformed to a range of 0-100, in which higher scores reflect better health status.

Countries

Austria

Outcome results

None listed

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