Intramuscular Temperature on the Echo-textural Characteristics

Cardenal Herrera University

Status

Enrolling

Conditions

Healthy Subjects

Treatments

Device: Muscle warm-up

Study type

Interventional

Funder types

Other

Identifiers

NCT06145646

CEEI23_453

Details and patient eligibility

About

Echointensity and echotexture have been used as a physiological marker for changes in skeletal muscle quality and structure caused by physical training, low activity, ageing and some neuromuscular disorders. However, there are some influencing factors on muscle echo-intensity and echotexture, such as temperature, which may not be taken into account when performing an ultrasound assessment and may alter the results.

This study aims to investigate the effects of muscle temperature on echointensity and other 2nd order echotextures variables such as homogeneity, contrast, correlation and entropy of muscle tissue, in order to gain a better understanding of this correlation and minimise its influence, which would allow greater precision in the use of muscle ultrasound as a diagnostic tool.

The methodology of this study includes firstly the acquisition of ultrasound images of the vastus lateralis muscle. This acquisition will be performed during the continuous recording of muscle temperature, carried out during a passive cooling process after 20 min of heating using microwave equipment. In addition, to standardise the results, a correction factor will be calculated to compensate for the influence of subcutaneous adipose tissue thickness on echogenicity and echotexture.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Acceptance of participation in the study.
Healthy subjects.
Subjects between the ages of 18 and 65.

Exclusion criteria

Have known neurological, cardiovascular, metabolic or orthopedic conditions that prevent them from participating in the study.
Present metal implants in the heating area.
Wear a pacemaker.
Perform physical activity during the 48 hours prior to data collection.
Contraindications of dry needling such as: Belonephobia, history of abnormal reaction to the puncture or injection, anticoagulant treatment or thrombocytopenia, lymphedema over the area of intervention, severely compromised immune system, vascular diseases, diabetes mellitus, pregnancy, epilepsy, allergy to metals or that the intervention area has wounds, scars, tattoos, or stains.