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Clinical Trials/NCT01673958
NCT01673958
Completed
Not Applicable

The Effect of Stair Descending and Stair Ascending Exercise on Muscle Strength and Performance: the SmartEscalator Device

European University Cyprus1 site in 1 country12 target enrollmentFebruary 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Aging
Sponsor
European University Cyprus
Enrollment
12
Locations
1
Primary Endpoint
Muscle strength (torque)
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The aim of the present project is to compare the acute and chronic effect of stair descending versus stair ascending exercise on muscle damage and performance in elderly males with chronic heart failure.

Detailed Description

Study design: Twelve elderly males with chronic heart failure, New York Heart Association class I-II, will participate in this study. Participants will be allocated into two equally-sized groups: a stair descending group (n = 6) and a stair ascending group (n = 6). At the beginning of the study, the volunteers will perform an acute bout of stair descending or stair ascending exercise on an automatic escalator (4 sets of 3 min each, speed will be set at 45 steps∙min-1). Step height will be 20.5 mm. Before and at day 2 post exercise, physiologic measurements will be performed and blood samples will be collected. Then, participants will carry out six weeks of stair descending or ascending training consisting of three exercise sessions per week (the first two weeks the speed will be set at 45 steps∙min-1, the next two weeks at 50 steps∙min-1 and the last two weeks at 55 steps∙min-1 for both groups). Afterward, they will repeat the acute stair descending or ascending protocol, as carried out at the beginning of the study, and the same physiologic measurements will be performed and blood samples will be collected. Measurements: Isometric (at 90 knee flexion), concentric and eccentric peak torque at 60o∙s-1of quadriceps femoris, pain-free range of motion, delayed onset muscle soreness and creatine kinase will be measured.

Registry
clinicaltrials.gov
Start Date
February 2012
End Date
April 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr. Anastasios Theodorou

Principal investigator

European University Cyprus

Eligibility Criteria

Inclusion Criteria

  • chronic heart failure (New York Heart Association class I-II)
  • subject provides written informed consent
  • personal physician of the participants provides written informed consent

Exclusion Criteria

  • consumed any nutritional supplement the last 3 months
  • performed intense eccentric exercise the last 6 months
  • non Caucasian

Outcomes

Primary Outcomes

Muscle strength (torque)

Time Frame: Change from baseline in muscle strength at day 2 post exercise at the first and sixth week of training

An isokinetic dynamometer (Cybex, Ronkonkoma, NY) will be used for the measurement of isometric, eccentric and concentric knee extensor peak torque at 90° knee flexion. The average of the three best maximal voluntary contractions with their dominant leg will be recorded. In order to ensure that the subjects provide their maximal effort, the measurements will be repeated if the difference between the lower and the higher torque value exceeded 10%. There will be two minutes rest between isometric efforts.

Secondary Outcomes

  • Pain free range of motion (degrees)(Before and at day 2 post exercise at the first and sixth week of training)
  • Creatine kinase, CK (activity IU)(Before and at day 2 post exercise at the first and sixth week of training)
  • Delayed onset muscle soreness, DOMS (scale 1-10)(Before and at day 2 post exercise at the first and sixth week of training)

Study Sites (1)

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