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Using Bedside Ultrasound to Screen for Sarcopenia in Older Adults

Using Bedside Ultrasound to Screen for Sarcopenia in Older Adults

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04370912
Enrollment
152
Registered
2020-05-01
Start date
2021-09-01
Completion date
2022-04-01
Last updated
2022-11-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sarcopenia

Brief summary

The loss of both muscle mass and quality with increasing age is called 'sarcopenia' and is a risk factor for falls, fractures and increased mortality. Sarcopenia is diagnosed with Dual-energy X-ray absorptiometry (DXA) scanning (according to current criteria), but in Canada DXA scans are not approved to screen for this condition. One potential solution is Point of Care Ultrasound (PoCUS), since recent advances have made bedside ultrasound technology readily available as a rapid bedside screening tool.

Detailed description

Some recent work has examined the possibility of using ultrasound as a measure of both muscle quantity and muscle quantity. Work done by Strasser et al, has shown that ultrasonic measures of muscle thickness in the quadriceps muscle has a highly significant correlation with maximal voluntary contration. Other work done by Miron-Mombiela et al has shown that measures of muscle thickness and echointensity (a measure of muscle quality) also show high correlations with grip strength. These findings (supported by our pilot data, see Pilot Data) and new technological advances in bedside ultrasonic devices suggest that these measures might be a valuable contribution to the process of screening for sarcopenia in older adults. In this proposal, Investigators hypothesize that bedside ultrasound, which is increasingly becoming a mainstream component of the standard physical exam, will be a much more specific and accurate alternative to our current best screening methods.

Interventions

DIAGNOSTIC_TESTBed side Ultrasound

Handgrip strength will be measured using a digital grip strength dynamometer (Sammons Preston, Nottinghamshire, UK). This measurement is carried out three times using the subject's dominant hand, and then averaged

Sponsors

Canadian Institutes of Health Research (CIHR)
CollaboratorOTHER_GOV
University of British Columbia
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum

Inclusion criteria

* each subject must be 65 years of age or greater

Exclusion criteria

* hemodialysis patients will be excluded, due to excessive fluid shifts with dialysis * patients using chronic oral corticosteroids will be excluded, due to potential muscle atrophy * hemiparesis due to a stroke or paresis of the lower limbs will be excluded * subjects with pitting edema on physical exam (due to liver, renal or heart failure) or patients that are severely dehydrated will be excluded * patients with myositis, systemic connective tissue disorders, systemic atrophies affecting the central nervous system (CNS) and CNS demyelinating diseases will be excluded

Design outcomes

Primary

MeasureTime frameDescription
US measurement for Sarcopeniathrough study completion, an average of 1 yearo establish PoCUS measures (muscle thickness, MT; echointensity, EI) as a new screening test for sarcopenia
Weight in kgthrough study completion, an average of 1 yearweight and height will be combined to report BMI in kg/m\^2
Height in cmthrough study completion, an average of 1 yearweight and height will be combined to report BMI in kg/m\^2
Handgrip strength in kgthrough study completion, an average of 1 yearHandgrip strength cutoffs for sarcopenia for men and women

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026