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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04451005
Other study ID # SARC-F
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 6, 2016
Est. completion date December 10, 2019

Study information

Verified date June 2020
Source University of Sao Paulo
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Sarcopenia is a generalized progressive skeletal muscle disorder that represents a related physiological vulnerability that is associated with or increases the likelihood of adverse outcomes, including falls, fractures, physical disability and death. The parameters used to assess sarcopenia in clinical practice have limited use due to their custody.

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.


Description:

Sarcopenia is a progressive and generalized skeletal muscle disorder that represents an age-related physiological vulnerability that is associated with an increased likelihood of adverse outcomes, including falls, fractures, physical disability and mortality. The parameters used to assess sarcopenia in clinical practice have limited use due to its cost.

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.


Recruitment information / eligibility

Status Completed
Enrollment 403
Est. completion date December 10, 2019
Est. primary completion date May 6, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria:

- Age = 60 years

- Sign free and informed consent;

- Demonstrate interest, conditions and availability to participate in all procedures included in the study protocol;

Exclusion Criteria:

- Refusal to participate;

- Patients who have not undergone cognitive testing;

- Physical amputation;

- Patients undergoing interventional treatment for sarcopenia;

Study Design


Related Conditions & MeSH terms


Intervention

Other:
0
Elderly patients with sarcopenia

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Sao Paulo

Outcome

Type Measure Description Time frame Safety issue
Primary Sarcopenia in the elderly Evaluation of sarcopenia in the elderly 12 months
Secondary Development of a new tool for sarcopenia screening Development of a new tool for sarcopenia screening 12 months
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