The participants are healthy and athletic people..
Conditions
Interventions
Intervention 1: Intervention group: bilateral cerebral anodal stimulation, duration of stimulation is 20 minutes and intensity is 2 milliamps, and it is applied in three consecutive sessions with a ti
Sponsors
Razi University of Kermanshah
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactEhsan Amiri
Razi University of Kermanshah
Outcome results
None listed