A System for Lengthening Contraction Training of Muscle
LCT
1 other identifier
interventional
36
1 country
1
Brief Summary
Evaluation of a new exercise machine designed to improve strength and speed of movement in the leg muscles. Investigators are trying to learn whether a new training method results in greater strength improvements as compared to a traditional method.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable healthy
Started Sep 2007
Longer than P75 for not_applicable healthy
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2007
CompletedFirst Submitted
Initial submission to the registry
December 14, 2007
CompletedFirst Posted
Study publicly available on registry
December 18, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2009
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2009
CompletedAugust 4, 2011
January 1, 2010
2.3 years
December 14, 2007
August 3, 2011
Conditions
Outcome Measures
Primary Outcomes (1)
Leg strength
16 weeks
Secondary Outcomes (1)
Ability to rise from a chair
16 weeks
Study Arms (2)
VSC-VLC
EXPERIMENTALvelocity-controlled variable resistance, lengthening contraction
SC
ACTIVE COMPARATORConstant weight shortening contraction
Interventions
Velocity-controlled variable resistance protocols enable trainees to load their muscles more optimally along the entire ROM in either or both of the shortening (VSC) and lengthening (VLC) phases of a training repetition
Eligibility Criteria
You may qualify if:
- healthy
- able to exercise 3 times per week for 16 weeks at Mobility Research Center
You may not qualify if:
- under- or overweight
- chronic disease that limits ability to exercise
- hips and legs limited by arthritis or pain
- presently engaged in a strenuous exercise program
- planned absence greater than one week.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Michiganlead
- BioLogic Engineering, Inc.collaborator
Study Sites (1)
Mobility Research Center
Ann Arbor, Michigan, 48105, United States
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Neil Alexander, MD
University of Michigan
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
December 14, 2007
First Posted
December 18, 2007
Study Start
September 1, 2007
Primary Completion
December 1, 2009
Study Completion
December 1, 2009
Last Updated
August 4, 2011
Record last verified: 2010-01