The effects of three consecutive sessions of non-invasive brain stimulation on sports performance in endurance train wome
Not Applicable
Recruiting
- Conditions
- The participants are healthy and athletic people..
- Registration Number
- IRCT20230925059509N1
- Lead Sponsor
- Razi University of Kermanshah
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 24
Inclusion Criteria
Age range from 18 to 35 years
Endurance train women with proper aerobic fitness and a history of at least one year of regular training
Body mass index (BMI) 18.5 to 24.9 kg per square meter of height
Being right-handed (preferred hand; be right-handed)
Exclusion Criteria
Having any cardiovascular, pulmonary and metabolic disease
History of seizures, epilepsy or other types of neurological diseases
The presence of implantable devices or pacemakers in the body
Smoking and alcohol consumption
Color blindness or color vision disorders
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 3 km time trail. Timepoint: Before and after the residual protocol and 24 hours after the residual protocol. Method of measurement: Recording time using a bicycle carmeter.;Vertical jump. Timepoint: Before and after the residual protocol and 24 hours after the residual protocol. Method of measurement: through the sargent jump test.;Rating of Perceived Exertion. Timepoint: Once every three minutes and at the end of the 3 km time trial. Method of measurement: Using a pressure perception scale of 0 to 100 borg.;Time to exhaustion. Timepoint: After finishing the submaximal residual activity. Method of measurement: Record the time and distance using a bicycle carmeter.;Amplitude of muscle electromyography. Timepoint: Every three minutes for 30 seconds. Method of measurement: 8-channel wireless electromyography device (model 85260 Noraxon, Scottsdale, AZ).
- Secondary Outcome Measures
Name Time Method Cognitive function. Timepoint: Before and after the residual protocol and 24 hours after the residual protocol. Method of measurement: Using color-word Stroop test.;Choice reaction time. Timepoint: Before and after the residual protocol and 24 hours after the residual protocol. Method of measurement: Using choice reaction time device.;Feel scale. Timepoint: Once every three minutes. Method of measurement: Using an 11-item emotion scale.;Pleasure Sensation scale. Timepoint: Once every three minutes. Method of measurement: Using a 6-item scale of perceived arousal.;Pain scale. Timepoint: Once every three minutes. Method of measurement: Using a visual analog scale of 0 to 10.