🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Spain / NCT06953401
Starting soon Observational

Muscle Activity of the Gastrocnemius and Soleus Muscles by Surface Electromyography.

NCT06953401 · tracked via the Priya Life Science Spain tracker
Phase
Observational
Started
2025-09-01
Last updated
2025-05-01

Condition(s) studied

Muscle ActivityElectromyographyLower Limb

Investigational drug(s) / intervention(s)

Muscle contraction protocol for electromyographic assessment

Muscle contraction protocol for electromyographic assessment: Participants will perform a set of standardized lower limb muscle contractions (isometric, concentric, and eccentric) involving the gastrocnemius and soleus muscles while lying on an examination table and in standing position both static and dynamic as well as walking. Surface electromyography (mDurance® sEMG system) will be used to record muscle activation during each phase. The task is designed for physiological measurement only and does not constitute a therapeutic intervention. Protocol includes 3 trials per muscle and side, using standardized test conditions.

Study summary

This cross-sectional, comparative study aims to evaluate and compare the surface electromyographic (sEMG) activity of the gastrocnemius (medial and lateral) and soleus muscles during static and dynamic contraction tasks. Participants will perform three tests-resting state, isometric, concentric, and eccentric contraction, and dynamic gait-with bilateral measurements. A subgroup analysis will examine muscle activity variations based on foot posture, using the Foot Posture Index (FPI). The study uses the validated mDurance® sEMG system to obtain objective data under controlled lab conditions. The findings will enhance understanding of the functional role of each muscle and could inform rehabilitation and injury prevention strategies.

Eligibility

Sex
ALL
Min age
18 Years
Max age
30 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Age between 18 and 30 years. * No history of severe musculoskeletal disorders in the lower limbs. * No recent surgery or injury in the last 6 months. * No dermatological conditions affecting electrode placement. * Not allergic to adhesives. * Ability to perform the task without limitation. •. No high-intensity exercise in the 12 hours before testing * Ability to provide informed consent and complete the assessment Exclusion Criteria: * Reduced lower limb mobility. * Neuromuscular or skeletal conditions affecting the calf region. * Intense physical activity 12 hours before testing. * Lack of informed consent.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Centro Universitario de Plasencia Plasencia Cáceres

More University of Extremadura trials in Spain

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 NCT06953401 on ClinicalTrials.gov ↗ ← All trials in Spain