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

Status

Completed

Conditions

Intervention / Treatment

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.

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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