- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00690547
Force Enhancement of Musculus Quadriceps Femoris During and After Excentric Muscle Activity in Vivo
November 27, 2009 updated by: German Research Foundation
Force Enhancement of m. Quadriceps Femoris During and After Excentric Muscle Activity in Vivo by Maximal and Sub-maximal Deliberately Activation.
Force enhancement (FE) describes the phenomenon of strength potentialization of a muscle cell or the complete muscle during and after active extension compared to the strength of an isometric contraction with same muscle length.
The underlying physiological mechanism of this phenomenon is not completely known today.
In vitro trials indicate that the interaction of an active and a passive component on the cellular level are responsible for the higher strength measurements.
So far FE could be shown in vitro and in vivo on muscle fibers and small human muscles.
Further research is needed for verification of the existence of FE in voluntary motor activity in everyday life.
In order to approach this objective the investigators will scrutinize the functionality of the deliberately activated musculus (m) quadriceps femoris during and after active extension on the basis of in vivo studies.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
The research proposal is resubmitted with no amendments made regarding content.
Study Type
Observational
Enrollment (Anticipated)
60
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
-
-
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Munich, Germany, 80809
- Technical University of Munich, Department of Biomechanics in Sports
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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
20 years to 40 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Sampling Method
Non-Probability Sample
Study Population
males without previous muscular or neurophysiological diseases at an age between 20 and 40 years
Description
Inclusion Criteria:
- Males without previous muscular or neurophysiological diseases
- Age between 20 and 40 years
Exclusion Criteria:
- Previous muscular or neurophysiological diseases
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
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Test Group
|
activation of the muscle quadriceps femoris
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Identification of a potential Force enhancement by complex muscle activity with a high relevance for everyday life, for example more agile leg stretching (knee bend).
Time Frame: 12 months
|
12 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Evidence of existence of the force enhancement by deliberately activated, great human muscle by sub-maximal activation
Time Frame: 12 months
|
12 months
|
Correlation between typ of muscle fiber and force enhancement in vivo
Time Frame: 12 months
|
12 months
|
Analysis of the alternation of length of the muscle fiber during and after excentric extension for the differentiated explanation of in vivo mechanism excentric and post-excentric strength
Time Frame: 12 months
|
12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ansgar Schmirtz, Prof. Dr., Technical University of Munich, Department of Biomechanics in Sports
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
October 1, 2008
Primary Completion (Anticipated)
October 1, 2010
Study Completion (Anticipated)
October 1, 2010
Study Registration Dates
First Submitted
May 30, 2008
First Submitted That Met QC Criteria
June 3, 2008
First Posted (Estimate)
June 4, 2008
Study Record Updates
Last Update Posted (Estimate)
November 30, 2009
Last Update Submitted That Met QC Criteria
November 27, 2009
Last Verified
November 1, 2009
More Information
Terms related to this study
Other Study ID Numbers
- DFG27112007
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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