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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01400347
Other study ID # EMGMarko
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date July 2012
Est. completion date December 2013

Study information

Verified date November 2009
Source State University of New York - Upstate Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

It is generally accepted that the effectiveness of an exercise can be controlled not only by the weight or resistance applied but also by doing an exercise that would better target the desired muscle. The purpose of this study is to obtain objective information regarding selected lower extremity muscle activity during specific exercise and the influence of fatigue and speed on muscular activation.


Description:

It is generally accepted that the effectiveness of an exercise can be controlled not only by the weight or resistance applied but also by doing an exercise that would better target the desired muscle. Information regarding selected lower extremity muscle activity during specific exercise and the influence of fatigue and speed on muscular activation may enhance exercise prescription for all parties involved. Specifically, selection of specific training or rehabilitation exercises may be guided by increased awareness of specific muscle activation patterns during common exercises. Methods and Measures: Healthy subjects between 18 - 35 years old will be recruited from the community by a sample of convenience and word of mouth. Potential participants will report to the Institute for Human Performance. The potential participants will be asked to complete all documentation including informed consent, and health screening questionnaire. The qualified participants will be familiarized with the set up and specific exercises. If eligible, surface EMG recordings will be collected from the back extensors, gluteal muscles (buttocks), hamstrings (posterior thigh), quadriceps (anterior thigh), and gastrocnemius (calf) during squat and lunges exercises. For data analysis, a within subject measures analysis will be conducted using general linear models. Specifically, we will use paired t-tests and an analysis of variance (ANOVA). When applicable, post-hoc tests will be used to uncover differences among the groups of subjects on descriptor variables such as age, height, weight, rate of perceived exertion, and maximal and sub-maximal voluntary muscle performance variables (i.e. EMG amplitude, frequency). The statistical significance level will be set at alpha = 0.05 for all analyses performed.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2013
Est. primary completion date July 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - Healthy adults age 18-35 Exclusion Criteria: - Subjects who report any significant respiratory-cardiovascular disease, which is not yet under control. - Known orthopedic risks to strength training exercise

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States The Institute for Human Performance Syracuse New York

Sponsors (1)

Lead Sponsor Collaborator
State University of New York - Upstate Medical University

Country where clinical trial is conducted

United States, 

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