Effects of strength training with Vascular Occlusion associated with Electrical Stimulatio
Not Applicable
- Conditions
- Muscle developmentG11.427.578
- Registration Number
- RBR-8vvpztm
- Lead Sponsor
- niversidade Estadual Paulista Júlio de Mesquita Filho - Instituto de Biociências
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Will be included in the study participants of both sexes; aged between 18 and 45 years; physically active
Exclusion Criteria
Body Mass Index (BMI) above 30; alterations in sensibilities and mental disturbances that may alter the results or be harmful to the subject; risk factors for thromboembolism; who have a family history of deep vein thrombosis or pulmonary embolism; who have hypertension (blood pressure at rest > 140/90 mmHg)
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Muscle thickness before and after the interventions will be evaluated by means of ultrasonography through the images that will be obtained through the GE Voluson I system (GE Healthcare, Zipf, Austria) in two-dimensional mode (B) with linear transducer. All muscle thickness measurements will be performed by a previously trained investigator. For the evaluation, participants will be positioned in dorsal decubitus to avoid hip rotation and both limbs, dominant and non-dominant, will be evaluated. To obtain the image, conductive gel will be used for better reproduction of the images and the measurement of the distance between the anterior superior iliac spine and the upper border of the patella will be standardized by means of a vertical line. Then, the rectus femoris and the vastus intermedius will be measured from 50% of this distance.
- Secondary Outcome Measures
Name Time Method