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Detection of Muscle Quality in Children - Protocol for a Validation Study

Use of Ultrasound Echo Intensity for the Detection of Muscle Quality in Children - Protocol for a Validation Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06792279
Enrollment
120
Registered
2025-01-24
Start date
2025-03-01
Completion date
2026-03-31
Last updated
2025-01-24

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

Conditions

Ultrasonography

Brief summary

The goal of this observational study is to evaluate the validity and reliability of ultrasound echo intensity (EI) as a diagnostic tool for assessing muscle quality in children aged 10-14 years, including normal-weight, obese, and trained young athletes. The main questions it aims to answer are: Can EI reliably and accurately measure muscle quality in children when validated against gold-standard techniques like DXA and isokinetic dynamometry? What are the age-, sex-, and fitness-specific benchmarks for EI to differentiate between normal and pathological muscle quality?

Interventions

None listed

Sponsors

Charles University, Czech Republic
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
10 Years to 14 Years
Healthy volunteers
Yes

Inclusion criteria

• Generally healthy children

Exclusion criteria

* Acute illnesses * Chronic or acute diseases of the endocrine or musculoskeletal systems * Post-traumatic conditions

Design outcomes

Primary

MeasureTime frameDescription
Echo intensity of the vastus lateralis (VL) and rectus femoris (RF) musclesThrough study completion, an average of 1 yearEcho intensity will be measured by greyscale analysis derivered from ultrasound imaging.

Secondary

MeasureTime frameDescription
Skeletal Muscle MassThrough study completion, an average of 1 yearMeasured using DXA (Horizon DXA platform, Hologic)
Muscle StrengthThrough study completion, an average of 1 yearAssessed via isokinetic and isometric knee extensor strength using a Humac Norm isokinetic dynamometer

Countries

Czechia

Contacts

Primary ContactMichal Steffl, PhD
michal.steffl@ftvs.cuni.cz+420778701882

Outcome results

None listed

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