Ireland
--:--IST
Recruiting Not applicable

High-definition Surface Electromyography Markers for the Diagnosis of Sarcopenia

NCT04987814 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2022-05-18
Last updated
2025-05-23

Condition(s) studied

Sarcopenia

Investigational drug(s) / intervention(s)

HD-sEMG- Quadriceps muscle ultrasoundIPAQ Physical Activity Questionnaire.

HD-sEMG: high definition surface electromyography, allowing the recording of muscle activation signals sensitive to the intensity of the contraction and indirectly to the muscle strength as well as to the muscular fatigability, but also capable of measuring the modifications of the recruitment modalities of the motor units. This recording will be made on the rectus femoris during knee extension, either in the lying position or during chair lifts, depending on the patient's functional state.

- Quadriceps muscle ultrasound: Muscle Ultrasound with Philips Lumify Wireless Handheld Ultrasound for Android - Model - L12-4 linear probe, allowing performance at the patient's bed.

IPAQ Physical Activity Questionnaire.: physical activity assessment questionnaire/adapted version for seniors

Study summary

Sarcopenia is a progressive and generalised skeletal muscle disorder involving the accelerated loss of muscle mass and function that is associated with increased adverse outcomes including falls, functional decline, frailty, and mortality.

In this pilot project, the investigators want to explore the potential of the high-definition surface electromyography technology (HD-sEMG) for the diagnosis of sarcopenia.

This is a monocentric, descriptive, cross-sectional, parallel group study to develop a new diagnostic method.

It is planned to include 50 people aged 75 years and over hospitalized in the acute geriatric ward and suspected of sarcopenia (Score ≥4 on the SARC-F screening questionnaire).

The inclusion duration will be 36 months and adding a 1-month patient follow-up as part of routine care, the total study duration will be 37 months.

Patients will have their body composition (muscle mass, fat mass, and bone mass) using dual X-ray absorptiometry (DEXA). Muscular strength will be assessed by handgrip strength. Physical performance will be assessed. Additional data will be collected from their medical records.

Eligibility

Sex
ALL
Min age
75 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Patient aged 75 years and over * Score ≥4 on the SARC-F screening questionnaire * Enrolled in a social security plan (no AME) * Informed and consenting patient Exclusion Criteria: * BMI ≥30 kg/m2 * Untreated/unbalanced endocrinological pathology * Myopathy * Inflammatory or autoimmune pathology * Severe psychiatric pathology or severe cognitive disorders that do not allow the performance of examinations * Patients who are dependent for all acts of daily life * Patients with a very short life expectancy * Recent fracture or trauma of the lower limbs preventing dynamic measurement of HD-sEMG recording * Bilateral hip prosthesis * Skin problem that may interfere with the recording of surface EMG activity * Patient under guardianship / curatorship

Primary outcome measure(s)

  • Electromyographic signals of the rectus femoris collected by the HD-sEMG technique — day1-day7
    These signals will be confronted by the diagnosis of sarcopenia defined by the joint presence of the 2 clinical criteria of the European Working Group on Sarcopenia in Older People 2 (EWGSOP2).

Trial sites (6)

FacilityCityRegionStatus
Service de gériatrie aigue polyvalente (GAP) Ivry-sur-Seine France Recruiting
Service de soins de suite et de réadaptation Gériatrique 1 Ivry-sur-Seine France Recruiting
Service de soins de suite et de réadaptation gériatrique 2 Ivry-sur-Seine France Recruiting
Unité d'Explorations fonctionnelles du sujet âgé, Hôpital Charles Foix Ivry-sur-Seine France Not Yet Recruiting
Service de soins de suite et de réadaptation -Plaies et cicatrisation Paris France Recruiting
Service de soins de suite et de réadaptation Gériatrique Hôpital Rothschild Paris France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04987814 on ClinicalTrials.gov ↗ ← All trials in France