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The effects of acute non-invasive brain stimulation on cognitive and executive functions in one bout of exhaustive endurance activity in semi-endurance runners

The effects of acute non-invasive brain stimulation on cognitive and executive functions in one bout of exhaustive endurance activity in semi-endurance runners

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230629058614N1
Enrollment
18
Registered
2023-12-20
Start date
2023-05-05
Completion date
Unknown
Last updated
2024-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

The effect of acute non-invasive brain stimulation on cognitive and executive functions in a single bout of endurance exercise..

Interventions

Intervention group: 14 adult semi-endurance male runners, members of the Kermanshah athletics team. The first session will be used to familiarize the subjects with the research process, the method of
Subjects will be randomly exposed to two types of brain stimulation for 20 minutes, including 1) anodal stimulation of the left posterolateral prefrontal cortex (DLPFC) and 2) sham stimulation..

Sponsors

Razi University of Kermanshah
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1) More than 3 years of active experience in the field of endurance biathlon 2) Age range from 18 to 35 years 3) Body mass index (BMI) 18.5 to 24.9 kilograms per square meter of height 4) Not suffering from color blindness or color vision disorders 5) Being right-handed

Exclusion criteria

Exclusion criteria: 1) Suffering from any cardiovascular, pulmonary and metabolic diseases 2) history of seizures, epilepsy or other types of neurological diseases 3) The presence of implantable devices or pacemakers in the body 4) Smoking and alcohol consumption

Design outcomes

Primary

MeasureTime frame
Changes in bimanual coordination. Timepoint: Measurement of bimanual coordination at the beginning of the study in the first week (before the start of the intervention), measurement of bimanual coordination 20 minutes after stimulation, measurement of bimanual coordination one week after the first intervention and before the sham intervention in the second week, measurement Bimanual coordination 20 minutes after sham intervention (unrealistic stimulation) in the second week. Method of measurement: Lafayette company's two-handed coordination tool.;Reaction Time. Timepoint: Measurement of reaction time at the beginning of the study in the first week (before the start of the intervention), measurement of reaction time 20 minutes after stimulation, measurement of reaction time one week after the first intervention and before sham intervention in the second week, measurement of reaction time 20 minutes after From sham intervention (unreal stimulation) in the second week. Method of measurement: Reaction time device Response Panel (63035A, Lafayette, Indiana).;Working memory. Timepoint: Measurement of working memory at the beginning of the study in the first week (before the start of the intervention), measurement of working memory 20 minutes after stimulation, measurement of working memory one week after the first intervention and before sham intervention in the second week, measurement of working memory 20 minutes After sham intervention (unreal stimulus) in the second week. Method of measurement: Stroop word-color test.;Rate of perceived pressure (RPE). Timepoint: During the execution of sub-maximal endurance activity, every 3 minutes, the level of perceived pressure is announced and recorded by the subjects. The average pressure perception in each training session is calculated and used for analysis. Method of measurement: From the image of the Borg scale (0 – 100; RPE).;Feeling scale to measure the feeling of pleasure (perceptual response). Timepoint: During the perfo

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehdi esmaili

Razi University

m.esmaeili.2911@gmail.com+98 83 3836 2077

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026