Dynamic Electrostimulation on the Abdominal Muscles in Healthy Individuals

Universidad de León

Status: Completed

Conditions: Healthy

Treatments: Device: WB-EMS (Whole body electrostimulation); Device: WB-EMS off; Device: EMS

Study type: Interventional

Funder types: Other

Identifiers

NCT05117203

ETICA-ULE-009-2020

Details and patient eligibility

About

To determine the immediate effects on the abdominal musculature, assessed by ultrasound (RUSI), due to the application of electrostimulation using whole body electrostimulation together with physical exercise in healthy people and to compare with the application of local EMS in the abdominal area and the same physical exercise session. The same intervention is carried out for the control group as the WB-EMS group but simulated.

Full description

Evaluation of the immediate changes in the thickness of the abdominal muscles (Transversus abdominis, Internal and External Oblique and Rectus abdominis) and in the Interrectus distance after the physical exercise session together with whole body electrostimulation or local electrostimulation assessed by ultrasound (RUSI) in healthy people.

Enrollment: 120 patients

Sex: All

Ages: 18 to 35 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Healthy participants
• Good medical history without injury or chest pain in the past year
• No surgeries in the previous year.

Exclusion criteria

• Upper body mass index 30 Kg/m2
• Level of professional or elite sports activity
• Hyperventilation / hypercapnia and score above 23 points on the Nijmegen questionnaire
• Present any contraindication regarding the WB-EMS/EMS
• Viral o bacterial infections
• Arterial circulatory disorders, advanced arteriosclerosis
• Women during their menstrual period
• Type I diabetes, hemophilia, bruises, bleeding, cognitive deficit, fibromyalgia, congenital diseases with muscle-skeletal alterations at the level of the back and lower extremities, scoliosis, protrusion or disc herniation, medication consumption, abdominal surgeries (scars or keloids), abdominal muscle injury.
• Presence of chronic low back, hip or thigh pain

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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120 participants in 3 patient groups

WB-EMS group

Experimental group

Treatment:

Device: WB-EMS (Whole body electrostimulation)

EMS group

Experimental group

Treatment:

Device: EMS

Control group

Sham Comparator group

Treatment:

Device: WB-EMS off