Exercise Clinical Trial
Official title:
The Effect of Acute Concurrent Exercise on Inhibitory Control: An Event-related Potential Study
Verified date | April 2024 |
Source | National Taiwan Normal University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The present study aimed to determine the effects of acute concurrent exercise on inhibitory control via behavioral and event-related potential approaches and to examine its potential mediational role on lactate among younger adults. The main questions it aims to answer are: (1) Does acute concurrent exercise improve inhibitory control via behavioral and event-related potential approaches? (2) Does lactate play a potential mediational role in the effect of acute concurrent exercise on inhibitory control?
Status | Completed |
Enrollment | 78 |
Est. completion date | February 15, 2022 |
Est. primary completion date | August 15, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 20 Years to 30 Years |
Eligibility | Inclusion Criteria: - aged between 20 and 30 years - able to exercise without undue risk (i.e., the first seven questions of the Physical Activity Readiness Questionnaire for Everyone [PAR-Q+] were answered "No") - right-handed dominance - typical or corrected-to-typical eyesight - limited physical activity in the previous month (i.e., < 150 minutes/week of moderate-intensity physical activity) Exclusion Criteria: - psychiatric or neurological ailments - cardiorespiratory or neuromuscular conditions - obese status (body mass index [BMI] > 27 kg/m2) |
Country | Name | City | State |
---|---|---|---|
Taiwan | Department of Physical Education and Sport Sciences, National Taiwan Normal University | Taipei |
Lead Sponsor | Collaborator |
---|---|
National Taiwan Normal University |
Taiwan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Inhibitory control | Inhibitory control was assessed using a modified computerized version of the Stroop test, which was administered through Neuroscan Stim2 software (Compumedics Neuroscan, Charlotte, NC). The test comprised four blocks, each consisting of 108 trials. Within each block, three types of trials were presented: neutral, congruent, and incongruent. The neutral trial involved displaying a square printed in red, green, or blue color. The congruent trial presented Chinese language prints in corresponding colors and words [i.e., ? (RED), ? (GREEN), or ? (BLUE)]. In contrast, the incongruent trial displayed Chinese language prints in different colors and words [e.g., ? (RED) printed in blue color]. Each block included 36 neutral trials, 36 congruent trials, and 36 incongruent trials. Participants were instructed to respond promptly and accurately to the color of the stimulus presented. Subsequently, the mean response time (RT) of correct trials and accuracy for each Stroop condition were examined. | 30 minutes | |
Secondary | Blood lactate | Blood lactate levels were assessed using fingertip samples measured with a lactate analyzer (The EDGE, Taipei, Taiwan) at three distinct time points: Timepoint 1 (prior to the commencement of treatment), Timepoint 2 (17 minutes after the initiation of treatment), and Timepoint 3 (30 minutes after the start of treatment). | Timepoint 1 (prior to the commencement of treatment), Timepoint 2 (17 minutes after the initiation of treatment), and Timepoint 3 (30 minutes after the start of treatment). |
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