Osteosarcopenia and Exercise

NCT ID: NCT04526327

Last Updated: 2020-08-25

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

27 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-12-03

Study Completion Date

2019-10-01

Brief Summary

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The purpose of this study is to assess the efficacy of combination of aerobic and resistive exercise on activities of daily living and risk of fall in osteosarcopenic patients

Detailed Description

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After being informed about the study and potential risk, all patients giving written informed consent will undergo study entry.

to begin with: assessment with bioelectrical body composition analyzer and first exercise and assessment clinical scales

1th month: assessment with bioelectrical body composition analyzer and assessment clinical scales 3th month: assessment with bioelectrical body composition analyzer and assessment clinical scales

Conditions

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Sarcopenia Osteoporosis, Osteopenia

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Female and male patients over 70 years of age followed-up from osteoporosis outpatient clinic
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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exercise group

Female and male patients over 70 years of age with osteoporosis and sarcopenia

Group Type OTHER

exercise

Intervention Type OTHER

the combination of aerobic and resistive exercise, three time a week

Interventions

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exercise

the combination of aerobic and resistive exercise, three time a week

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Over 70 years of age
* Clinical diagnosis of osteoporosis or osteopenia
* Independent mobilization
* Walking speed \< 0.8 m / sec
* Grip strength \< 20 kg for women, \< 30 kg for men

Exclusion Criteria

* Uncontrolled hypertension (systolic blood pressure\> 200 mmHg, diastolic blood pressure\> 110 mmHg)
* Uncontrolled diabetes mellitus
* Stroke, hip fracture, knee and hip arthroplasty, spinal surgery in the last 6 months
* Severe cardiac arrhythmia
* Myocardial infarction in the last 6 months
* Severe dementia and difficulties in cooperation
* Cardiac pacemaker
* Dialysis
* Acute infection
* Severe edema
* Malignancy patients
* Severe anemia (Hgb \<8 mg / dl)
Minimum Eligible Age

70 Years

Maximum Eligible Age

91 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Sisli Hamidiye Etfal Training and Research Hospital

OTHER

Sponsor Role lead

Responsible Party

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Selda Çiftci

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Figen Yılmaz

Role: STUDY_CHAIR

Şişli Hamidiye Etfal Training and Research Hospital

Locations

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Şişli Hamidiye Etfal Training and Research Hospital

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2189

Identifier Type: -

Identifier Source: org_study_id

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