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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05148351
Other study ID # Universidad Católica de Murcia
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 17, 2022
Est. completion date October 1, 2022

Study information

Verified date October 2022
Source Catholic University of Murcia
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Frailty and sarcopenia are two age-related syndromes which can result in adverse health-related events. The combination of both is more predictive of mortality than either condition alone. These conditions can be reversed through an early detection and appropriate interventions. Nevertheless, scientific community highlights the lack of cheap, portable, rapid and easy-to-use tools for detecting frailty and sarcopenia in combination. The aim of this study is to validate an iPhone App to detect frailty and sarcopenia syndromes in community dwelling older adults. This is a protocol study of a retrospective diagnostic test accuracy study which will include at least 400 participants older than 60 years recruited from elderly social centers of Murcia city. Researchers will recollect data of health status, dependency, cognitive status, and functional capacity of the participants. The index test will consist in the measurement of muscle power exerted during a single Sit-to-stand through an App (iPhone), combined with calf and mid-upper arm circumference. The reference standard will be frailty syndrome and sarcopenia assessed according to Fried's phenotype and to the European Working Group on Sarcopenia in Older People 2 (EWGSOP2) (2019) recommendations, respectively. Sensitivity, specificity, positive predictive value, negative predictive values, and area under the curve will be reported.


Recruitment information / eligibility

Status Completed
Enrollment 775
Est. completion date October 1, 2022
Est. primary completion date October 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria: - Community-dwelling older adults living in the Region of Murcia Exclusion Criteria: - Barthel Index < 90 pts. - Mini-Cog test < 3 pts. - Severe cardiovascular problems - Pacemaker - Automatic defibrillator

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Spain Catholic University of Murcia Murcia

Sponsors (1)

Lead Sponsor Collaborator
Catholic University of Murcia

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Muscular power Muscular power generated by participants will be measured using an App (Sit-to-stand App version 1.1) installed on an iPhone (Apple Inc., USA).
During the execution, subjects will sit on a rigid chair with their arms crossed over their chest with the hip, knee and ankle joints at approximately 90 degrees. Subjects will be asked to stand-up as fast as possible. Participants will complete three STS repetitions. No footwear will be allowed during the test.
Cross-sectional baseline
Primary Frailty Syndrome Frailty Syndrome will be assessed according to Fried's Phenotype, which focuses on:
Handgrip strength
Usual gait speed
Weight loss
Exhaustion
Physical activity levels
Subjects who will result positive to three out of five criteria will be considered as "frail", whereas if they will result positive to only one or two of them they will be considered as "pre-frail". The absence of each criteria will be necessary to define a subject as "robust".
Cross-sectional baseline
Primary Sarcopenia Sarcopenia will be assessed according to the recommendation provided by the European Working Group on Sarcopenia in Older People 2 (EWGSOP2) (2019). This guideline focuses on the assessment of:
Leg muscle strength
Muscle mass quantity
Physical performance
The presence of low muscle strength levels will be considered as "probable sarcopenia"; the presence of low muscle mass and strength levels will be considered as "confirmed sarcopenia"; finally, the presence of the three criteria will be considered as "severe sarcopenia".
Cross-sectional baseline
Primary Calf and mid-upper arm circumference Researchers will measure subjects' calf and mid-upper arm circumference using a tape measure. Cross-sectional baseline
Secondary Subjects' clinical status Subjects' clinical status will be assessed through a list of questions regarding:
socioeconomic level
educational level
chronic pathologies
smoking habits
polypharmacy
depression
number of falls
hospitalization
self-perceived health status
Cross-sectional baseline
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