- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05314699
The Order Effect of Acute Concurrent Exercise on Executive Function: An Event-Related Potential Study
March 29, 2022 updated by: Yu-Kai Chang, National Taiwan Normal University
Executive function is a high-level cognition which plays an important role in our life.
Meta-analysis study has demonstrated that acute exercise could improve executive function.
However, it is still unclear whether executive function can be enhanced by the concurrent exercise that combines aerobic and resistance exercise.
Moreover, the sequence of concurrent exercise may result in different blood lactate concentration which may affect executive function.
Therefore, the purposes of present study are: (1) Measuring the order effect of acute concurrent exercise on executive function.
(2) Measuring whether order effect of acute concurrent exercise on executive function is mediated by blood lactate.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Executive function is a high-level cognition which plays an important role in academic performance, career, and interpersonal relationship.
Meta-analysis study has demonstrated that acute exercise could improve executive function, and also observed similar positive effect through both aerobic and resistance exercise.
However, it is still unclear whether executive function can be enhanced by the concurrent exercise that combines aerobic and resistance exercise.
Moreover, the sequence of concurrent exercise may result in different blood lactate concentration which may affect executive function.
Therefore, the purposes of present study are: (1) Measuring the order effect of acute concurrent exercise on executive function.
(2) Measuring whether order effect of acute concurrent exercise on executive function is mediated by blood lactate.
Study Type
Interventional
Enrollment (Actual)
99
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Taipei, Taiwan, 106
- Department of Physical Education and Sport Sciences, National Taiwan Normal University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years to 28 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- no history of psychiatric or neurological disorders
- no history of cardiovascular disease
- normal or corrected to normal vision and normal color perception
- right handed
- 18.5 < BMI < 27
Exclusion Criteria:
1. Diagnosed with epilepsy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: reading control group, RC
Participants conduct reading for 35 minutes.
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Experimental: resistance-aerobic exercise group, RA
Participants conduct 5-min warm up, 13-min resistance exercise, 12-min aerobic exercise, and 5-min cool down.
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Participants conduct 5-min warm up, 13-min resistance exercise, 12-min aerobic exercise, and 5-min cool down.
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Experimental: aerobic-resistance exercise group, AR
Participants conduct 5-min warm up, 12-min aerobic exercise, 13-min resistance exercise, and 5-min cool down.
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Participants conduct warm up for 5-min, aerobic exercise for 12-min, resistance exercise for 13-min, and 5-min cold down.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
task switch test
Time Frame: 30 minutes
|
The shifting aspect of executive function was assessed by means of a computer version of the task-switching test.
In brief, each participant was presented with six blocks of 64 trials.
For the first block, the participant was required to identify whether the stimulus (i.e., digits 1-9, without digit 5) within the solid-line square was greater/less than the digit 5.
For the second block, the participant identified whether the stimulus within the dotted-line square was even/odd.
The blocks 3-6 consisted of an equal number of stimuli from the first and second blocks forming an alternating-runs paradigm.
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30 minutes
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Stroop test
Time Frame: 30 minutes
|
The Stroop task consists of neutral, congruent, and incongruent trials.
In neutral trials, colored rectangles were presented and participants were instructed to respond to whether the squares were red, blue, or green.
For congruent and incongruent trials, participants were presented with the names of the three Chinese color words of 紅 (red), 藍 (blue), or 綠 (green) printed in either the same (congruent) or different (incongruent) ink color and instructed to respond to the color of the ink while inhibiting the meaning of the word.
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30 minutes
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
blood lactate
Time Frame: 1 minutes
|
The lactic acid system is one of the important systems of human energy metabolism.
In addition to supplying energy to muscles, it can also be used as an energy source for brain energy metabolism.
When people doing exercise, the concentration of blood lactate will be increased, and the lactate acid system will replace the glucose system as the main energy source for the brain.
In the present study, blood lactate were collected from fingertip with a lancet and measured by lactate analyzer before, 17 minutes after, and after intervention.
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1 minutes
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 15, 2021
Primary Completion (Actual)
November 29, 2021
Study Completion (Actual)
February 15, 2022
Study Registration Dates
First Submitted
March 29, 2022
First Submitted That Met QC Criteria
March 29, 2022
First Posted (Actual)
April 6, 2022
Study Record Updates
Last Update Posted (Actual)
April 6, 2022
Last Update Submitted That Met QC Criteria
March 29, 2022
Last Verified
March 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- PACNL_rueihongli_CE_Order
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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