Validity of an App to Detect Frailty and Sarcopenia Syndromes in Elderly
Validity of an iPhone App to Detect Frailty and Sarcopenia Syndromes in Community Dwelling Older Adults: Protocol for a Diagnostic Accuracy Study
1 other identifier
observational
775
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2022
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 25, 2021
CompletedFirst Posted
Study publicly available on registry
December 8, 2021
CompletedStudy Start
First participant enrolled
February 17, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2022
CompletedOctober 24, 2022
October 1, 2022
8 months
November 25, 2021
October 21, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
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
Frailty Syndrome
Frailty Syndrome will be assessed according to Fried's Phenotype, which focuses on: 1. Handgrip strength 2. Usual gait speed 3. Weight loss 4. Exhaustion 5. 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
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: 1. Leg muscle strength 2. Muscle mass quantity 3. 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
Calf and mid-upper arm circumference
Researchers will measure subjects' calf and mid-upper arm circumference using a tape measure.
Cross-sectional baseline
Secondary Outcomes (1)
Subjects' clinical status
Cross-sectional baseline
Eligibility Criteria
At least 400 community-dwelling older adults, older than 60 y/o and living in the Region of Murcia (Spain) will be recruited.
You may qualify if:
- Community-dwelling older adults living in the Region of Murcia
You may not qualify if:
- Barthel Index \< 90 pts.
- Mini-Cog test \< 3 pts.
- Severe cardiovascular problems
- Pacemaker
- Automatic defibrillator
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Catholic University of Murcia
Murcia, 30107, Spain
Related Publications (3)
Ruiz-Cardenas JD, Rodriguez-Juan JJ, Martinez-Garcia MDM, Montemurro A. Comparing Sarcopenia Definitions and Muscle Power Reduction: Associations with Health Outcomes in Spanish Community-Dwelling Older Adults. J Clin Med. 2024 Aug 23;13(17):4988. doi: 10.3390/jcm13174988.
PMID: 39274199DERIVEDRuiz-Cardenas JD, Montemurro A, Martinez-Garcia MDM, Rodriguez-Juan JJ. Sit-to-Stand Video Analysis-Based App for Diagnosing Sarcopenia and Its Relationship With Health-Related Risk Factors and Frailty in Community-Dwelling Older Adults: Diagnostic Accuracy Study. J Med Internet Res. 2023 Dec 8;25:e47873. doi: 10.2196/47873.
PMID: 38064268DERIVEDMontemurro A, Ruiz-Cardenas JD, Martinez-Garcia MDM, Rodriguez-Juan JJ. Validity of an iPhone App to Detect Prefrailty and Sarcopenia Syndromes in Community-Dwelling Older Adults: The Protocol for a Diagnostic Accuracy Study. Sensors (Basel). 2022 Aug 11;22(16):6010. doi: 10.3390/s22166010.
PMID: 36015771DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Juan D Ruiz-Cárdenas
Catholic University of Murcia
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
November 25, 2021
First Posted
December 8, 2021
Study Start
February 17, 2022
Primary Completion
October 1, 2022
Study Completion
October 1, 2022
Last Updated
October 24, 2022
Record last verified: 2022-10
Data Sharing
- IPD Sharing
- Will not share