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Clinical Trials in Turkey / NCT07738588
Starting soon Not applicable

Wireless EMG-Based Monitoring of Paraspinal Muscle Activation in Adolescent Idiopathic Scoliosis

NCT07738588 · tracked via the Priya Life Science Turkey tracker
Sponsor
Ertugrul Deniz Kose
Phase
Not applicable
Started
2026-09-01
Last updated
2026-07-31

Condition(s) studied

Adolescent Idiopathic Scoliosis (AIS)

Investigational drug(s) / intervention(s)

Wireless Embedded Surface EMG (sEMG) Measurement System

Wireless Embedded Surface EMG (sEMG) Measurement System: A custom-developed, low-power, wireless, non-invasive surface EMG system consisting of skin-surface electrodes, an analog front-end (AFE) for signal conditioning and digitization, and a microcontroller-based wireless communication module. Electrodes are placed bilaterally on the paraspinal muscles at the apical vertebra level, approximately 3 cm lateral to the spinous process. EMG signals are sampled at ≥1000 Hz using a differential (bipolar) configuration and analyzed for root mean square (RMS), mean absolute value (MAV), and frequency-domain (FFT) parameters to quantify muscle activation asymmetry between the convex and concave sides of the spinal curve.

Study summary

This study aims to develop and evaluate a wireless, non-invasive, embedded electromyography (EMG) system for monitoring paraspinal muscle activation asymmetries in adolescents with idiopathic scoliosis. Surface EMG electrodes will be placed bilaterally around the apical vertebra of the spinal curve to record muscle activity during static (seated) and dynamic (trunk extension) tasks. Measurements will be taken longitudinally over the course of physiotherapy treatment to evaluate whether the recorded muscle activity patterns can serve as an objective, non-invasive indicator of treatment response, potentially reducing reliance on repeated radiographic (X-ray) follow-up.

Eligibility

Sex
ALL
Min age
10 Years
Max age
18 Years
Healthy volunteers
No
Inclusion Criteria: * Diagnosed with adolescent idiopathic scoliosis * Cobb angle between 10° and 25° * No prior surgical or conservative treatment for scoliosis Exclusion Criteria: * Neurological disease * Significant concomitant orthopedic problems * Back pain severe enough to interfere with the measurement process

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Amasya University Amasya Amasya

Other trials for the same condition

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 NCT07738588 on ClinicalTrials.gov ↗ ← All trials in Turkey