- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01614392
Lower Extremity Muscle and Function in the Elderly: Study 2
December 6, 2018 updated by: Roger A Fielding, Tufts University
This research study is looking to compare the effects of two uniquely different power training interventions (high force, lower velocity versus low force, high velocity) on changes in mobility status among older individuals at risk for mobility disability.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
52
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
-
-
Massachusetts
-
Boston, Massachusetts, United States, 02111
- Jean Mayer USDA Human Nutrition Research Center on Aging
-
-
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
70 years to 85 years (Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Male and Female 70-85 yrs
- Community dwelling
- Short Performance Battery Score >9
- BMI range 19-32 kg/m2
- Willingness to be randomized and come the laboratory for 20 weeks.
Exclusion Criteria:
- Acute or Terminal Illness
- MI in previous 6 months, symptomatic coronary artery disease or congestive heart failure.
- Upper or Lower extremity fracture in previous 6 months
- Uncontrolled hypertension (150/90mmHg)
- Neuromuscular diseases and drugs that affect neuromuscular function
- Hormone replacement therapy
- Participation in any regular endurance or resistance training exercise during previous 3 months
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
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: High velocity low force Power Training
Lower Extremity high velocity power training performed at lower external resistance (40% of the 1 repetition maximum muscle strength).
Leg and knee extension exercises were performed twice per week (3 sets of each exercise consisting of 10 repetitions).
|
Lower Extremity high velocity power training performed at lower external resistance (40% of the 1 repetition maximum muscle strength).
Leg and knee extension exercises were performed twice per week (3 sets of each exercise consisting of 10 repetitions).
|
|
Experimental: Low velocity high force Power Training
Lower extremity low velocity power training performed at high external resistance (70% of the 1 repetition maximum muscle strength).
Leg and knee extension exercises were performed twice per week (3 sets of each exercise consisting of 10 repetitions).
|
Lower extremity low velocity power training performed at high external resistance (70% of the 1 repetition maximum muscle strength).
Leg and knee extension exercises were performed twice per week (3 sets of each exercise consisting of 10 repetitions).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Leg Extensor Muscle Power
Time Frame: Change from baseline to Week 16
|
Leg extensor muscle power measured on pneumatic strength testing equipment at a external force consistent with 70% of the participant maximum leg extensor strength.
|
Change from baseline to Week 16
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Roger A Fieilding, Ph D., Jean Mayer USDA Human Nutrition Research Center on Aging
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
September 1, 2009
Primary Completion (Actual)
October 1, 2011
Study Completion (Actual)
October 1, 2011
Study Registration Dates
First Submitted
September 28, 2009
First Submitted That Met QC Criteria
June 5, 2012
First Posted (Estimate)
June 7, 2012
Study Record Updates
Last Update Posted (Actual)
December 10, 2018
Last Update Submitted That Met QC Criteria
December 6, 2018
Last Verified
December 1, 2018
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- AG-18844
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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