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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05113758
Other study ID # ABZ-ECO-2018-01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 28, 2019
Est. completion date June 30, 2022

Study information

Verified date August 2023
Source Complejo Hospitalario Universitario de Albacete
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Observational prospective study in older adults admitted to an Acute Geriatric Unit, in which sarcopenia will be evaluated by ultrasound in the anterior rectus femoris muscle.


Description:

The main objective of the study is to estimate, by means of portable ultrasound, parameters of muscle quantity and quality (anterior rectus femoris muscle area, width and echostructure ) in older adults hospitalized in Acute Geriatric Units for medical reasons.


Recruitment information / eligibility

Status Completed
Enrollment 161
Est. completion date June 30, 2022
Est. primary completion date June 30, 2022
Accepts healthy volunteers No
Gender All
Age group 69 Years and older
Eligibility Inclusion Criteria: - Patients over 69 years of age. - Hospitalization for a medical cause in Acute Geriatric Units. - Holden's Functional Ambulation Classification Scale at level 1 or higher. - Informed consent signed by the patient or legal representative. Exclusion Criteria: - Terminal condition or life expectancy of less than 6 months. - Impossibility or refusal to undergo muscle ultrasound. - Refusal for follow-up - Severe dementia stage Global Deteriorating Scale: 7 - Impossibility in the opinion of the investigators to complete the necessary data for the study.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
muscle ultrasound
All participants will undergo a muscle ultrasound on admission and at discharge

Locations

Country Name City State
Spain Complejo Hospitalario Universitario de Albacete Albacete

Sponsors (7)

Lead Sponsor Collaborator
Pedro Abizanda Hospital Infanta Sofia, Hospital Universitario Getafe, Hospital Universitario Infanta Leonor, Hospital Universitario La Paz, Hospital Virgen del Valle de Toledo, Puerta de Hierro University Hospital

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence of sarcopenia on admission Prevalence of sarcopenia on admission. A prevalent case of sarcopenia will be considered if a patient fulfills the EWGSOP2 at admission 72 hours
Primary Incidence of sarcopenia between admission and discharge An incident case of sarcopenia will be considered if a patient not fulfilling EWGSOP2 diagnostic criteria on admission, will meet diagnostic criteria at discharge of sarcopenia at discharge (diagnosis will be considered as a dichotomous variable -yes/no-). 15 days
Primary Muscle mass (the anterior rectus femoris muscle) The evolution of muscle mass between admission and discharge will be assessed by ultrasound 15 days
Secondary Minimal nutritional assessment (MNA-SF) score The mini-nutritional assessment - short form is a simple, non - invasive and validated scale for the detection of malnutrition in older adults. It takes into account the patient's loss of appetite, weight loss, motor skills, recent health status, neuropsychological disorders. The maximum score of the MNA-SF is 14:
Greater than or equal to 11: normal nutritional status. Between 8 and 11: risk of malnutrition. Less than 8: malnutrition.
72 hours
Secondary Hand grip strength Using a hand-held dynamometer 15 days
Secondary 4-meter walking speed test The evolution of the value of the 4-meter walking speed test between admission and discharge will be assessed. 15 days
Secondary ADL (Activities of Daily Living) questionnaire the ADL questionnaire will also be performed on admission, at discharge, and at 3 months. 3 months
Secondary SPPB score (SHORT PHYSICAL PERFORMANCE BATTERY score) Short Physical Performance Battery (SPPB): score range 0-12, higher score means a better outcome 15 days
Secondary Mortality Mortality will be measured with vital status at 3 months. 3 months
Secondary Length of stay, days Day of admission to day of discharge 15 days
Secondary Readmission(s) after index hospitalization Readmission(s) after index hospitalization, Dichotomous outcome (yes/no) 3 months
Secondary Emergency department (ED) visit(s) ED visit(s) after index hospitalization, Dichotomous outcome (yes/no) 3 months
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