- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01672281
vibroX-training in Endurance Trained Men
May 13, 2013 updated by: University of Zurich
Influence of vibroX-training on the Power-duration-relationship and Maximal Force in Relation to Conventional Resistance Training in Endurance Trained Men
In endurance sports competitions such as cycling, an athlete's capacity to sustain submaximum power (i.e.
endurance capacity) strongly influences overall race performance.
Endurance capacity can be increased by both long, continuous endurance exercise at moderate oxygen consumption, and high-intensity (at or above peak oxygen consumption) interval training.
However, it has also been shown that resistance exercise, if performed in addition to endurance exercise, can further enhance endurance capacity.
The investigators have recently described a novel training method, which is based on combined vibration and resistance training and superimposed vascular occlusion.
Based on the investigators previous results showing that this type of training leads to marked increases in endurance capacity in previously untrained young women, the investigators aim at investigating whether the method is also effective in increasing endurance capacity in highly endurance-trained young men, and whether the method leads to bigger improvements relative to resistance exercise alone.
Besides the functional outcomes the investigators are also interested in the specificity of the cellular adaptations with respect to the two trainings methods.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
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 Locations
-
-
ZH
-
Zurich, ZH, Switzerland, 8091 Zurich
- University Hospital Zurich, Division of Neurology
-
-
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 35 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion criteria:
- male
- no fever / no common cold at the beginning of the study
- at least 4 endurance training sessions prior to beginning of study
- age 18-35y
- non-smoker
- no cardiological / orthopedic problems
- no pacemaker
- fulfills health questionnaire's requirements
Exclusion criteria: female
- fever / common cold at beginning of study
- untrained condition (less than 4 endurance training sessions prior to the
- beginning of the study)
- age under 18 oder above 35y
- smoker
- cardiovascular or orthopedic problems
- cardiac pacemaker
- does not fulfill health questionnaire's requirements
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
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: vibrox training
|
Comparison between two exercise interventions
Other Names:
|
|
Experimental: resistance training
|
Comparison between two exercise interventions
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline in Critical Power
Time Frame: 2 month intervention
|
The difference in changes in Critical Power [Watts] are compared between the vibrox- and resistance training group.
For this purpose, participants complete pre and post training a cycling ramp test and 4 cycling constant load tests.
|
2 month intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Hans H. Jung, Professor MD, University Hospital Zurich, Division of Neurology
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.
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
November 1, 2011
Primary Completion (Actual)
September 1, 2012
Study Completion (Actual)
December 1, 2012
Study Registration Dates
First Submitted
May 25, 2012
First Submitted That Met QC Criteria
August 21, 2012
First Posted (Estimate)
August 24, 2012
Study Record Updates
Last Update Posted (Estimate)
May 14, 2013
Last Update Submitted That Met QC Criteria
May 13, 2013
Last Verified
May 1, 2013
More Information
Terms related to this study
Other Study ID Numbers
- vbx
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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