- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05905081
Acute Effects of Moderate Intensity Aerobic Exercise on Cognitive Functions in Young Adult Males
September 12, 2023 updated by: Şermin Tükel Akay, Izmir University of Economics
Acute Effects of Physical Fitness and Aerobic Exercise on Cognitive Functions in Young Adult Males
60 healthy male university students will be included in this study.
Physical fitness parameters, fluid intelligence, and physical activity level will be measured at baseline.
Participants will be randomised to one of two testing schedules, groups will complete either a 30-minutes aerobic exercise session or a resting control condition.
Cognitive measures (simple reaction time task, go/nogo task, spatial cueing, n-back task) will be tested before and after the intervention.
Study Overview
Study Type
Interventional
Enrollment (Actual)
61
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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İzmir, Turkey
- Izmir University of Economics
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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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- No known psychiatric, cognitive or physical health problems
- No limiting issue for performing exercise according to Physical Activity Readiness Questionnaire (PAR-Q+)
- Physical activity level according to International Physical Activity Questionnaire (IPAQ) < 3000 MET
Exclusion Criteria:
- Discomfort/illness that will interfere with physical activity
- Using any medication or stimulants
- Having limitations for performing exercise according to Physical Activity Readiness Questionnaire (PAR-Q+)
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: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Exercise Group
30-minutes moderate-intensity aerobic exercise will be performed according to ACSM guidelines
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30-minutes aerobic exercise intervention on the bicycle ergometer.
The exercise protocol includes 5 minutes of warm-up, 20 minutes of loading and 5 minutes of cool-down.
The intensity of the exercise will be adjusted to be between 46% and 63% of the VO2max calculated according to the exercise programming guide published by the American College of Sports Medicine (ACSM), and the perceived effort level on the Borg scale will be 12-13.
Warm-up and cool-down periods will be set to 46% of VO2max and Borg perceived exertion level below 9.
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No Intervention: Control Group
30-minutes video screening while sitting
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in motor inhibition
Time Frame: Baseline and 30 mins after baseline
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Go/NoGo Task
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Baseline and 30 mins after baseline
|
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Change in working memory capacity
Time Frame: Baseline and 30 mins after baseline
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N-Back Task
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Baseline and 30 mins after baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in psychomotor rate
Time Frame: Baseline and 30 mins after baseline
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Simple reaction time task
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Baseline and 30 mins after baseline
|
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Change in visual inspection and attention
Time Frame: Baseline and 30 mins after baseline
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Spatial cueing
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Baseline and 30 mins after baseline
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
International Physical Activity Questionnaire (IPAQ)
Time Frame: At baseline
|
IPAQ score under 300 indicates low physical activity, 300-3000 indicates moderate physical activity and higher than 3000 is high physical activity.
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At baseline
|
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VO2max
Time Frame: At baseline
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Astrand test
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At baseline
|
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Raven's Progressive Matrices
Time Frame: At baseline
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Fluid intelligence
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At baseline
|
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Muscle strength
Time Frame: At baseline
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back-chest-leg strength
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At baseline
|
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Plank test
Time Frame: At baseline
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muscular endurance
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At baseline
|
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T-test
Time Frame: At baseline
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agility
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At baseline
|
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Body composition
Time Frame: At baseline
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Body Mass Index (BMI)
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At baseline
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Şermin Tükel Akay, PhD, Izmir University of Economics
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 20, 2023
Primary Completion (Actual)
September 1, 2023
Study Completion (Actual)
September 1, 2023
Study Registration Dates
First Submitted
May 3, 2023
First Submitted That Met QC Criteria
June 14, 2023
First Posted (Actual)
June 15, 2023
Study Record Updates
Last Update Posted (Actual)
September 13, 2023
Last Update Submitted That Met QC Criteria
September 12, 2023
Last Verified
September 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 4930-GOA
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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