- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06621550
Effect of High-Intensity Interval Training Exercise on Cognitive Function of Young Adults
September 29, 2024 updated by: Freddy Man Hin LAM, The Hong Kong Polytechnic University
The Effect of High-Intensity Interval Training Exercise on Cognitive Function of Young Adults: A Pilot Randomized Controlled Trial
To explore the sustainability of the acute effect of High Intensity Interval Training (HIIT) on executive function in young adults.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
70
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 Contact
- Name: Freddy Man Hin LAM, PhD
- Phone Number: +852 27666720
- Email: freddy-mh.lam@polyu.edu.hk
Study Locations
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-
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Hung Hom, Hong Kong
- Recruiting
- The Hong Kong Polytechnic University
-
Contact:
- Freddy Man Hin LAM
- Phone Number: +852 27666720
- Email: freddy-mh.lam@polyu.edu.hk
-
-
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:
- Young adult aged 18-40 years old
- No visionary defect or other sensory condition including uncorrected refractive defect and color blindness refraining the individual to be assessed by the tasks
Exclusion Criteria:
- With known neurological, cardiovascular, or other physical and mental conditions that limit the ability to safely participate in high-intensity interval training
- With known specific learning disabilities
- Known drug or alcohol abuse problems
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: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: HIIT Arm
Participants will receive a single session of HIIT, which lasts for 19 minutes
|
Participants will receive a single session of HIIT, which last for 19 minutes in duration.
During the HIIT session, participants will complete 2 minutes stretching warm-up exercise, followed by a video of exercises which will be projected on the screen to facilitate the participants to follow.
The exercise in the video involves various combinations of aerobic and core resistance exercise such as squat jump, jump lunge, push up, burpee, mountain climber etc.
The exercise involved bodyweight or minimal basic equipment only, the workout to rest ratio is 45 secs: 15 secs.
Participants' heart rate will be kept surveillance and to maintain their respective heart rate attained 85% of aged predicted maximal heart rate during the workout period.
|
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No Intervention: Control Arm
Participants will be arranged to rest quietly on a chair for 19 minutes.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stroop task
Time Frame: From baseline to 72 hours post intervention
|
Stroop Task is a neurocognitive test for the performance on inhibition control.
Participants are shown a series of word colors that are either congruent or incongruent with the color of the word itself.
The participant is required to respond to the color of the word and not the word itself.
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From baseline to 72 hours post intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Flanker Task
Time Frame: From baseline to 72 hours post intervention
|
Flanker Task is a neurocognitive test for the performance on inhibition control.
Participants are shown a series of arrows.
The participant is to respond to which way the center arrow is pointing; whether it is to the right or to the left
|
From baseline to 72 hours post intervention
|
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Trail making test (TMT)
Time Frame: From baseline to 72 hours post intervention
|
TMT is a neurocognitive test for the performance on cognitive flexibility.
There are part A and part B in the TMT.
The time required to completed part A as well as part B would be recorded separately, the difference in time in completing part B and part A (B-A) and the ratio of time in completing part A and part B (B/A) would be used as the interference score.
|
From baseline to 72 hours post intervention
|
|
Wisconsin Card Sorting test (WCST)
Time Frame: From baseline to 72 hours post intervention
|
WCST is a neurocognitive test for the performance on cognitive flexibility.
Participants will be presented with four response cards, which are of different geometric properties (number of objects, color of object and shape of objects), and one stimulus card at a time.
Participants will be required to sort the stimulus card.
There are 30 trials in the test, number of correct sorting will be recorded, and accuracy will be obtained as number of correct sorting divided by 30.
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From baseline to 72 hours post intervention
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Change in accuracy as measured by the 2-back task
Time Frame: From baseline to 72 hours post intervention
|
2-back task is a neurocognitive test for the performance on working memory.
Participants are presented with a sequence of stimuli in character form.
The task consists of indicating when the current stimulus matches the one from 2 steps earlier in the sequence.
There are 48 trials in the task, the number of correct responses will be recorded.
The accuracy will be obtained as number of correct responses divided by 39.
|
From baseline to 72 hours post intervention
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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 1, 2024
Primary Completion (Estimated)
December 1, 2024
Study Completion (Estimated)
December 1, 2024
Study Registration Dates
First Submitted
September 29, 2024
First Submitted That Met QC Criteria
September 29, 2024
First Posted (Actual)
October 1, 2024
Study Record Updates
Last Update Posted (Actual)
October 1, 2024
Last Update Submitted That Met QC Criteria
September 29, 2024
Last Verified
September 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- HSEARS20231129004
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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