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Validation of Muscle Strength Testing for Pectoralis Major

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01636115
First Posted: July 10, 2012
Last Update Posted: December 7, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Hsin-Min Lee, National Science Council, Taiwan
  Purpose
This study wants to understand which direction of shoulder movement and what posture of shoulder are best for the procedure of muscle strength testing of the muscle pectoralis major(PM). We will use muscle activity signals (sEMG) and force measurement to analyze the contribution of two parts of PM in three different contraction direction with three different shoulder postures.

Condition
Pectoralis Major Muscle Strength Surface EMG Force Measurement

Study Type: Observational
Study Design: Observational Model: Case-Crossover
Time Perspective: Prospective
Official Title: Validation of Muscle Strength Testing for Pectoralis Major

Further study details as provided by Hsin-Min Lee, National Science Council, Taiwan:

Primary Outcome Measures:
  • sEMG [ Time Frame: 6/1/2012 ]
    Surface EMG signal were collected.


Enrollment: 24
Study Start Date: May 2012
Study Completion Date: November 2012
Primary Completion Date: November 2012 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   17 Years to 30 Years   (Child, Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Students in University.
Criteria

Inclusion Criteria:

  • Young male subjects which could expose the area of anterior chest to paste the sEMG electrodes

Exclusion Criteria:

  • Injury and uncomforted one week before the test
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01636115


Locations
Taiwan
I-Shou university
Kaohsiung, Taiwan
Sponsors and Collaborators
National Science Council, Taiwan
  More Information

Responsible Party: Hsin-Min Lee, Associate Professor, National Science Council, Taiwan
ClinicalTrials.gov Identifier: NCT01636115     History of Changes
Other Study ID Numbers: ISU-IRB-101-001
First Submitted: July 5, 2012
First Posted: July 10, 2012
Last Update Posted: December 7, 2012
Last Verified: December 2012