Clinical trial Recruiting at 1 site Interventional Ages 50 and up

Muscle Biomarkers and Early Management of Sarcopenia

Official title: Morphological and Functional Biomarkers of Skeletal Muscle Adaptations for Early Detection of Sarcopenia and of the Therapeutic Effects of a Home-Based Exercise Intervention: A Randomized-Controlled Trial

Run by I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio · NCT07692308 · Data updated 2026-11-12

This trial tests a non-invasive ultrasound-based method to measure muscle quality and pairs it with a home exercise program to see if it can help people over 50 with sarcopenia or at risk for it.

More Sarcopenia trials

Quick facts

Study typeInterventional
Ages50 Years and up
SexAll
Enrollment192 (estimated)
SponsorI.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
Academic / other
Drugs / interventionsradiation
Locations1 site (Milan, Mi)
StatusRecruiting
StartedJune 3, 2026
Main results expectedJune 3, 2027
Study endsJune 3, 2029
Registry record updatedJuly 13, 2026
Trial IDNCT07692308 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Sedentary adults over 50 with sarcopenia or at risk for sarcopenia, plus healthy older adults matched by age, sex, and activity level for reference.

Probably not a fit

Individuals unable to perform the exercise protocol or with conditions severely limiting participation may not experience measurable benefits.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The study investigates an integrated approach for early detection and management of sarcopenia using Quantitative Ultrasound with Radio-Frequency analysis (QUS-RF) to characterize muscle morphology and quality. QUS-RF measurements will be compared to standard assessments of body composition, strength, and physical performance. Participants will engage in a digitally delivered home-based exercise program with general physical activity guidance. The trial includes sedentary adults over 50 with sarcopenia, those at risk, and matched healthy controls to form a reference cohort. Primary aims include validating QUS-RF as an accessible diagnostic tool and observing potential improvements in muscle strength and function through the home-based intervention.

Why it matters

Potential benefit: If successful, the approach could enable earlier detection of sarcopenia and provide an effective, scalable home-based exercise strategy to preserve muscle health.

How similar studies have gone: Prior work has shown promise with non-invasive imaging and exercise programs in sarcopenia, but the combination with QUS-RF and a digital home-based intervention is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Sedentary individuals aged over 50 years.
* Individuals with sarcopenia, defined as reduced muscle mass assessed by bioelectrical impedance analysis and reduced muscle strength assessed by handgrip strength, according to EWGSOP2 criteria.
* Individuals at risk of sarcopenia, defined as reduced muscle mass with preserved muscle strength.
* Healthy age-, sex-, and physical activity-matched older adults eligible for inclusion in the reference cohort.
* Ability to understand the study procedures and provide written informed consent.

Exclusion Criteria:

* Hospitalization within the previous 6 weeks.
* Substance or alcohol abuse.
* Use of medications that may impair balance or coordination.
* Major locomotor impairments.
* Inability to complete the exercise protocol.
* Medical, cognitive, or functional conditions that, in the opinion of the investigators, may interfere with safe participation, adherence to the study procedures, or completion of the follow-up assessments.

Where it's running

  • IRCCS Ospedale Galeazzi-Sant'Ambrogio
    Milan, Mi, Italy
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.