- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05689606
Cortical Excitability, Cognitive Functions, and Peripheral Signaling Molecules
The Relationship of Cortical Excitability, Cognitive Functions, and Peripheral Signaling Molecules Following Acute Exercise
Study Overview
Detailed Description
Participants Twenty-eight healthy young adults (female|male:14|14) aged 20-30 years will have participated in the study.
Participants will be at least undergraduate students, right-handed dominant, exercising <150 minutes per week in the last six months. Before the experiment, the participants will be evaluated for their background, family history, and whether they have any health complaints that prevent them from exercising.
With the adult transcranial magnetic stimulation safety screening questionnaire, participants in the risk group for brain stimulation, those with intracranial implants and contraindications, and those with a history of any psychiatric or neurological disease, seizures, any serious medical condition, or pregnancy will be excluded. The hand preference questionnaire will evaluate hand preference, and physical activity status will be evaluated by the short version of the international physical activity questionnaire. The cardiorespiratory fitness will be assessed with the graded maximal exercise stress test. The N-back test is a continuous performance test used to assess working memory capacity. The mental rotation test will evaluate the mental rotation score. The research team designed both tests.
Transcranial magnetic stimulation will be used to assess corticomotor excitability. Resting Motor Threshold (RMT), Short Interval Intracortical Inhibition (SICI), and input-output curve measurements will be performed on all participants in our study for the TMS study.
BDNF and CTSB measurements of the participants will be made both at baseline and following the acute exercise.
HIIT exercise lasting 23 minutes will be performed on the bicycle ergometer. Participants will make 3 visits to the laboratory. First session: Cardiorespiratory fitness assessment, all questionnaires. Second session: TMS analyses, cognitive assessments, HIIT, myokine assessments Third session: TMS analyses, cognitive assessments, control (watching a nature documentary).
The second and third sessions will be performed by cross-over design. Data analysis will be performed with two-way repeated ANOVA to determine the effect of within-group factors (control and HIIT) and time (PRE and POST) on corticospinal excitability and other parameters. When the effect size was calculated as ɳp2 >0.26, the sample size was calculated a priori as n = 22. Considering possible data losses, the number of participants was determined as 28.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Ankara, Turkey
- Ankara City Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being right-handed
- Aged between 20 and 30 years
- Being sedentary
Exclusion Criteria:
- having intracranial implants
- history of psychiatric or neurological disease, seizure, any serious medical condition or pregnancy
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Exercise group
The exercise group performs acute high-intensity interval training.
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Exercise includes acute high-intensity interval training.
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|
No Intervention: Control group
The Control group includes the same participants.
In this session, they do not exercise, and they watch a nature documentary.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Short interval intracortical inhibition
Time Frame: Change from Baseline short interval intracortical inhibition immediately following acute exercise
|
The relative amplitude reduction of motor evoked potentials by subthreshold conditioning stimuli.
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Change from Baseline short interval intracortical inhibition immediately following acute exercise
|
|
Resting motor threshold
Time Frame: Change from Baseline resting motor threshold immediately following acute exercise
|
The amount of transcranial magnetic stimulation machine output necessary to produce a motor-evoked potential that exceeds a defined peak-to-peak amplitude.
Lower scores mean a better outcome.
|
Change from Baseline resting motor threshold immediately following acute exercise
|
|
Input output curve
Time Frame: Change from Baseline input output curve immediately following acute exercise
|
The input-output curve is a sigmoid-shaped relation between the MEP amplitude at incremented TMS intensities.
Higher scores mean a better outcome.
|
Change from Baseline input output curve immediately following acute exercise
|
|
Working memory
Time Frame: Change from Baseline working memory score immediately following acute exercise
|
The small amount of information that can be held in mind and used in the execution of cognitive tasks.
Higher scores mean a better outcome.
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Change from Baseline working memory score immediately following acute exercise
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Serum BDNF
Time Frame: Change from Baseline serum BDNF immediately following acute exercise
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Serum level of BDNF.
Higher scores mean a better outcome.
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Change from Baseline serum BDNF immediately following acute exercise
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|
Mental rotation
Time Frame: Change from Baseline mental rotation score immediately following acute exercise
|
The ability to transform a mental representation of an object so as to accurately predict how the object would look from a different angle.
Higher scores mean a better outcome.
|
Change from Baseline mental rotation score immediately following acute exercise
|
|
Serum Cathepsin B
Time Frame: Change from Baseline serum Cathepsin B immediately following acute exercise
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Serum level of Cathepsin B. Higher scores mean a better outcome.
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Change from Baseline serum Cathepsin B immediately following acute exercise
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 12091985
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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