Effects of Clinical Pilates and Whole Body Vibration Exercises in Postmenopausal Osteoporotic Women

NCT ID: NCT04259697

Last Updated: 2020-02-06

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

UNKNOWN

Clinical Phase

NA

Total Enrollment

34 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-01-15

Study Completion Date

2020-05-15

Brief Summary

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The aim is to compare the effects of clinical pilates and whole body vibration exercises in postmenopausal osteoporotic women on strength, flexibility, balance, bone turnover markers and quality of life.

Detailed Description

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The aim of this study is to compare the effects of clinical pilates and whole body vibration exercises in postmenopausal osteoporotic women in terms of strength, flexibility, balance, bone turnover markers and quality of life. Thirty-four women who are diagnosed with postmenopausal osteoporosis will be recruited into the study. Participants will be divided into two groups: (1) clinical pilates group, (2) vibration exercises group. Exercise programs will be performed two times per week for twelve weeks. The strength of the extensor muscles of the hip, knee, back, elbow will be measured with a hand-held dynamometer. Flexibility will be assessed measuring the fingertip-to-floor distance in flexion and lateral bending. The balance performance will be assessed using the timed up and go test, Tetrax fall index and the maximum hold time on unipedal stance and on tandem stance. The short form-12 questionnaire will be used to assess the quality of life. Also, bone turnover markers will be measured. All assessments will be performed before and after exercise programs.

Conditions

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Osteoporosis

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

A controlled study
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Clinical pilates

Exercises will be performed two times per week for twelve weeks.

Group Type EXPERIMENTAL

Clinical pilates

Intervention Type OTHER

Clinical pilates exercises will be performed progressively. The duration of each exercise session will be an average of 40 minutes initially and then will be increased to 60 minutes as the program progress.

Whole body vibration

Exercises will be performed two times per week for twelve weeks.

Group Type EXPERIMENTAL

Whole body vibration

Intervention Type OTHER

Whole body vibration exercises will be performed using the Power Plate pro5 AIRdaptive machine.The duration of each exercise session will be an average of 20 minutes initially and then will be increased to 30 minutes as the program progress.

Interventions

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Clinical pilates

Clinical pilates exercises will be performed progressively. The duration of each exercise session will be an average of 40 minutes initially and then will be increased to 60 minutes as the program progress.

Intervention Type OTHER

Whole body vibration

Whole body vibration exercises will be performed using the Power Plate pro5 AIRdaptive machine.The duration of each exercise session will be an average of 20 minutes initially and then will be increased to 30 minutes as the program progress.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Being in the postmenopausal period
* Having body mass index equal to or greater than 18,5 kg/m²
* A lack of regular exercise
* Having been diagnosed with osteoporosis
* Having the ability to walk independently

Exclusion Criteria

* Having a cardiopulmonary problem that may prevent participating in exercise programs
* Having kidney stones
* Being diagnosed with diabetes
* Presence of epilepsy
* Having cardiological problems such as arrhythmia, using a pacemaker, hypertension
* Having neurological disorders such as Parkinson, stroke, multiple sclerosis, neuropathy
* Having surgery in the last 6 months
Minimum Eligible Age

40 Years

Maximum Eligible Age

70 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Dokuz Eylul University

OTHER

Sponsor Role lead

Responsible Party

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Burcu Ece KORKMAZ

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Dokuz Eylul University, School of Physical Therapy and Rehabilitation

Izmir, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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Ece Korkmaz

Identifier Type: -

Identifier Source: org_study_id

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