Low Intensity Resistance Training With Vascular Occlusion in Coronary Heart Disease Patients

March 22, 2017 updated by: Borut Jug, University Medical Centre Ljubljana

Effect of Low Intensity Resistance Training With Vascular Occlusion on Muscle Hypertrophy, Neuromuscular Adaptations and Selected Cardiovascular Parameters in Patients With Coronary Heart Disease

In our clinical controlled trial, patients with coronary heart disease will be randomly assigned into the exercise intervention (low intensity resistance training with vascular occlusion) or usual physical activity group (control group).

Study Overview

Detailed Description

Physical activity in patients with coronary heart disease improves health, quality of life, and reduces risk of coronary events, morbidity and mortality. Aerobic training is preferred as a part of cardiac rehabilitation with its well established evidence-based guidelines. On the other hand, the resistance training was first introduced as a part of cardiac rehabilitation just over a decade ago, due to its positive effects on performance, quality of life and muscle hypertrophy and strength. Despite the positive effects of resistance training, there still lacks evidence about its effect on cardiovascular health. Furthermore, guidelines still do not specify the exact training volumes, doses and types of resistance training for patients with coronary heart disease.

In clinical practice, it is often difficult and contraindicated to use near-maximal loads (e.g., in the early stages of cardiac rehabilitation, after sport injury, etc.). Muscle atrophy and weakness often occur rapidly in the affected area due to the effects of trauma (or disease) and inactivity. Consequently, training modalities that promote hypertrophy or counteract atrophy without the use of heavy loads should be of special interest in the rehabilitation of some chronic diseases for which high musculoskeletal forces are contraindicated.

Occlusive strength training with tourniquet cuffs was first used nearly twenty years ago. Studies have shown that low to-moderate intensity (20-50% of 1RM) resistance training with vascular occlusion leads to gains in muscle strength and volume comparable to those seen after conventional heavy resistance training. This effects suggest, that ischemic strength training may be a useful method in rehabilitation and other contexts.

To conclude, the aim of this study is to compare the effect of low intensity resistance training with vascular occlusion vs. normal physical activity on:

  1. muscle hypertrophy, strength and neuromuscular parameters;
  2. vascular function;
  3. and blood parameters (anabolic and catabolic hormones, catecholamines, inflammations factors, parameters of oxidative stress etc.)

Study Type

Interventional

Enrollment (Anticipated)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Ljubljana, Slovenia, 1000
        • Recruiting
        • University Medical Centre
        • Contact:
        • Contact:
        • Principal Investigator:
          • Borut Jug, PhD, MD
        • Sub-Investigator:
          • Tim Kambič, BSc
        • Sub-Investigator:
          • Marko Novaković, MD
        • Sub-Investigator:
          • Katja Tomažin, PhD
        • Sub-Investigator:
          • Vojko Strojnik, PhD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 75 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • above 18 years old and below 75 years old
  • coronary heart disease documented with clinical event
  • stable coronary heart disease patients

Exclusion Criteria:

  • Unstable phase of coronary heart disease
  • dysfunction of left ventricle
  • residual myocardial ischemia
  • contraindications for physical activity,
  • intellectual development disorder,
  • recent dissection of aorta
  • recent vein thrombolysis

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
ACTIVE_COMPARATOR: Resistance training group
Patients to be randomly assigned to the "resistance training group" will have resistance training with vascular occlusion 2 times per week for a period of 8 weeks on unilateral leg extension machine. During each training, they will performed 3 sets of 15 repetitions at the intensity of 30% 1 RM (repetition maximum). Each training set will separated by a 30 second rest period.
Patients will perform unilateral leg extension resistance training with vascular occlusion 2 times per week for a period of 8 weeks. Each training session will consist of 3 sets of 15 repetitions at the intensity of 30% 1 RM with 30 s of rest period between sets.
NO_INTERVENTION: Control group
Patients to be randomly assigned to the control group (normal physical activity) will continue with their usual physical activity regime.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in maximal strength
Time Frame: 4 weeks, 8 weeks
Determined with one repetition maximum test on leg extension machine (kg)
4 weeks, 8 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in maximal voluntary contraction (MVC)
Time Frame: 4 and 8 weeks
Determined with modified interpolated twitch protocol
4 and 8 weeks
Changes of flow-mediated dilatation of the brachial artery
Time Frame: 4 weeks, 8 weeks
Measured with ultrasound in %
4 weeks, 8 weeks
Change in muscle hypertrophy (muscle thickness)
Time Frame: 4 and 8 weeks
Measured with ultrasound in mm
4 and 8 weeks
Change of the value of blood human growth hormon (HGH)
Time Frame: 4 and 8 weeks
measured in ng/mL
4 and 8 weeks
Change of the value of testosterone
Time Frame: 4 and 8 weeks
measured in ng/dL
4 and 8 weeks
Change of the value of myostatin
Time Frame: 4 and 8 weeks
measured in ng/mL
4 and 8 weeks
Change of the value of mechano growth factor (MGF)
Time Frame: 4 and 8 weeks
measured in ng/mL
4 and 8 weeks
Change of the value of insulin-like growth factor (IGF-1)
Time Frame: 4 and 8 weeks
measured in ng/mL
4 and 8 weeks
Change of the value of epinephrine
Time Frame: 4 and 8 weeks
measured in pg/mL
4 and 8 weeks
Change of the value of norepinephrine
Time Frame: 4 and 8 weeks
measured in pg/mL
4 and 8 weeks
Change of the value of cortisol
Time Frame: 4 and 8 weeks
measured in mcg/dL
4 and 8 weeks
Change in C-reactive protein
Time Frame: 4 and 8 weeks
measured in mg/L
4 and 8 weeks
Change in blood pressure prior and after exercise
Time Frame: 1-8 week
measured in mmHg
1-8 week
Change in heat-shock protein (HSP-72)
Time Frame: 4 and 8 weeks
measured in ng/mL
4 and 8 weeks
Change in resting and post-exercise heart rate
Time Frame: 4 and 8 weeks
Measured in beats per min
4 and 8 weeks
Change of from-the-questionnaire-obtained quality of life
Time Frame: 4 and 8 weeks
Measured in points
4 and 8 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

February 27, 2017

Primary Completion (ANTICIPATED)

June 15, 2017

Study Completion (ANTICIPATED)

June 15, 2017

Study Registration Dates

First Submitted

March 15, 2017

First Submitted That Met QC Criteria

March 21, 2017

First Posted (ACTUAL)

March 22, 2017

Study Record Updates

Last Update Posted (ACTUAL)

March 27, 2017

Last Update Submitted That Met QC Criteria

March 22, 2017

Last Verified

March 1, 2017

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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