Plyometric Training for Elderly Women

NCT ID: NCT02852642

Last Updated: 2016-08-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

37 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-03-31

Study Completion Date

2016-07-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Healthy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Exercise

Power training model based in the potentiation of the stretch-shortening cycle.

Group Type EXPERIMENTAL

Exercise

Intervention Type OTHER

Plyometric training

Control

Maintaining daily activities

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Exercise

Plyometric training

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

60 Years

Maximum Eligible Age

75 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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University of Sao Paulo

OTHER

Sponsor Role lead

Responsible Party

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João Pedro Pinho

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Alberto C Amadio, PhD

Role: STUDY_DIRECTOR

University of Sao Paulo

Other Identifiers

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PlyoElderly

Identifier Type: -

Identifier Source: org_study_id

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