- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02852642
Plyometric Training for Elderly Women
July 28, 2016 updated by: João Pedro Pinho, University of Sao Paulo
Structure and Musculoskeletal Function, Functional Capacity and Quality of Life of Elderly Women in Response to a Plyometric Training Model Based on the Stretch-shortening Cycle
Introduction: the physiological aging process induces several structural changes in the musculoskeletal system.
These, in turn, result in functional changes that are reflected in the senescent dependency, determining the reduction in their quality of life.
Power training has been identified as ideal to mitigate the effects of aging.
However, there are indications that an intervention based on the potentiation of the stretch-shortening cycle action is a better choice.
Study Overview
Detailed Description
Study hypotheses: the participants of the proposed intervention will increase their bone mineral density, muscle volume, functional capacity and will show some improvement in their gait, as well as in their quality of life.
Purposes: the main objective of this study was to propose a training model based in the potentiation of the stretch-shortening cycle action and assess its effects on selected parameters of musculoskeletal morphology, functional capacity and quality of life of elderly women.
Study Type
Interventional
Enrollment (Actual)
37
Phase
- Not Applicable
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
60 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- sedentary women, not using bone alteration medication physically able
Exclusion Criteria:
- attending less than 80% of the intervention sessions and not attending the final evaluation
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Exercise
Power training model based in the potentiation of the stretch-shortening cycle.
|
Plyometric training
|
No Intervention: Control
Maintaining daily activities
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
electromyography gait analysis
Time Frame: through study completion, an average of 6 months
|
Knee extensors and flexors muscles co-contraction during the gait cycle
|
through study completion, an average of 6 months
|
Bone microstructure
Time Frame: through study completion, an average of 6 months
|
Tibia and radius trabecular and cortical bone density
|
through study completion, an average of 6 months
|
body composition
Time Frame: through study completion, an average of 6 months
|
Lean and fat body mass
|
through study completion, an average of 6 months
|
gait kinematics
Time Frame: through study completion, an average of 6 months
|
toe clearance: minimum vertical distance of the forefoot and the ground during swing phase
|
through study completion, an average of 6 months
|
balance
Time Frame: through study completion, an average of 6 months
|
Center of pressure displacement
|
through study completion, an average of 6 months
|
function capacity assessment
Time Frame: through study completion, an average of 6 months
|
timed up and go test
|
through study completion, an average of 6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Alberto C Amadio, PhD, University of Sao Paulo
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
March 1, 2016
Primary Completion (Actual)
July 1, 2016
Study Completion (Actual)
July 1, 2016
Study Registration Dates
First Submitted
July 22, 2016
First Submitted That Met QC Criteria
July 28, 2016
First Posted (Estimate)
August 2, 2016
Study Record Updates
Last Update Posted (Estimate)
August 2, 2016
Last Update Submitted That Met QC Criteria
July 28, 2016
Last Verified
July 1, 2016
More Information
Terms related to this study
Other Study ID Numbers
- PlyoElderly
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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