- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06602700
Effects of High-intensity Interval Training and Moderate-intensity Continuous Training on Functioning of Attentional Networks and Heart Rate Variability in Healthy Adults
September 15, 2024 updated by: Beijing Sport University
This study investigated the effects of HIIT and MICT on functioning of attentional networks and explored the relationship between heart rate variability (HRV) and these networks in healthy adults.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
36
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
-
-
Haidian district
-
Beijing, Haidian district, China, 100084
- Sports, Exercise and Brain Sciences Laboratory, Sports Coaching College, Beijing Sport University, Beijing 100084, China
-
-
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:
- normal or corrected-to-normal vision
- normal auditory function without any reading disorders
- right-handed
Exclusion Criteria:
- color blindness
- color weakness
- dyslexia
- history of smoking
- cardiovascular diseases
- personal or family history of mental illness
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: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: HIIT intervention
|
high-intensity interval training
|
|
Experimental: MICT intervention
|
moderate-intensity continuous training
|
|
No Intervention: Rest control
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
reaction times of the ANT-I task
Time Frame: immediately after interventions
|
ANT-I: Attention Network Test for Interactions
|
immediately after interventions
|
|
accuracy of the ANT-I task
Time Frame: immediately after interventions
|
ANT-I: Attention Network Test for Interactions
|
immediately after interventions
|
|
HR
Time Frame: immediately after interventions
|
HR: heart rate
|
immediately after interventions
|
|
heart rate variability
Time Frame: immediately after interventions
|
immediately after interventions
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
February 22, 2023
Primary Completion (Actual)
September 30, 2023
Study Completion (Actual)
December 31, 2023
Study Registration Dates
First Submitted
September 13, 2024
First Submitted That Met QC Criteria
September 15, 2024
First Posted (Estimated)
September 19, 2024
Study Record Updates
Last Update Posted (Estimated)
September 19, 2024
Last Update Submitted That Met QC Criteria
September 15, 2024
Last Verified
September 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2023067H
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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