Diagnostic Evaluation of Sarcopenia in Elderly Patients
NCT ID: NCT04451005
Last Updated: 2020-06-30
Study Results
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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COMPLETED
403 participants
OBSERVATIONAL
2016-05-06
2019-12-10
Brief Summary
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In this perspective, this study proposes or develops a tool for the diagnosis of having sarcopenia with a specific boa and a sensitive boa.
low cost and useful.
Elderly patients (n = 403) from the Geriatrics Outpatient Clinic of Hospital das Clínicas, Faculty of Medicine, University of São Paulo will be selected
This study was of clinical importance, due to sarcopenia and a relevant factor, and could lead to consequences and poor prognosis in patients with gold, and it was not a method of clinical practice to properly endorse body composition in this population.
Detailed Description
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In this perspective, this study proposes the development of a tool for the diagnosis of having sarcopenia with good specificity and good sensitivity and of low cost and useful.
Elderly patients (n = 403) from the Geriatrics Outpatient Clinic of Hospital das Clínicas, Faculty of Medicine, University of São Paulo will be selected. After signing the informed consent, sarcopenia will be assessed using the reference method (DXA) and anthropometry. The data obtained by the methods are treated statistically to obtain correlation and thus a new tool for the evaluation of sarcopenia patients in the elderly can be developed.
This study is of clinical importance, as sarcopenia is a relevant factor and can lead to consequences and poor prognosis in elderly patients, and there is no low-cost method in clinical practice to properly assess body composition in this population.
Conditions
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Keywords
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Study Design
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OTHER
PROSPECTIVE
Study Groups
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Elderly patients with sarcopenia
Elderly patients with sarcopenia
0
Elderly patients with sarcopenia
Interventions
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0
Elderly patients with sarcopenia
Eligibility Criteria
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Inclusion Criteria
* Sign free and informed consent;
* Demonstrate interest, conditions and availability to participate in all procedures included in the study protocol;
Exclusion Criteria
* Patients who have not undergone cognitive testing;
* Physical amputation;
* Patients undergoing interventional treatment for sarcopenia;
60 Years
ALL
Yes
Sponsors
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University of Sao Paulo
OTHER
Responsible Party
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Dan Linetzky Waitzberg
Principal researcher
Other Identifiers
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SARC-F
Identifier Type: -
Identifier Source: org_study_id