- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07256847
Effect of 6-Week High Intensity Interval Training on VO2max, Physical Competence and Sleep Quality in Sedentary Male University Students
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
None Selected
-
Hong Kong, None Selected, Hong Kong
- SSPE, The Chinese University of Hong Kong
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- university students;
- daily sedentary time > 8 hours;
- healthy individuals who are capable of physical tests or HIIT;
- no regular exercise habits;
- can understand English or Chinese.
Exclusion Criteria:
- self-reported history of neurological, psychiatric, or medical diseases;
- current intake of medications and/or recreational drugs that could affect the central nervous system and/or the ability to learn.
Study Plan
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: High-intensity interval training (HIIT) group
A 6-week HIIT exercise plan (running). Duration: Each session consists of 10 x 1-minute high-intensity bouts interspersed with 10 x 1-minute recovery periods. Adding the 3-minute warmup and 3-minute cool-down, each session totals approximately 26 minutes. This protocol is followed for 6 weeks. Intensity: High-intensity bouts are performed at 80-90% of HRmax (RPE 15-18). Recovery periods are at 40-50% of HRmax (RPE 11-13). Warm-up and cool-down are at 50% HRmax (RPE 11-13). Modality: Running, jogging, or brisk walking, either on a treadmill or outdoors. Supervision: The first three sessions are supervised in a laboratory setting. Subsequent sessions are unsupervised and performed at home with heart rate monitoring and remote data tracking via Polar Flow for Coach. |
A 6-week HIIT exercise plan (running). Duration: Each session consists of 10 x 1-minute high-intensity bouts interspersed with 10 x 1-minute recovery periods. Adding the 3-minute warmup and 3-minute cool-down, each session totals approximately 26 minutes. This protocol is followed for 6 weeks. Intensity: High-intensity bouts are performed at 80-90% of HRmax (RPE 15-18). Recovery periods are at 40-50% of HRmax (RPE 11-13). Warm-up and cool-down are at 50% HRmax (RPE 11-13). Modality: Running, jogging, or brisk walking, either on a treadmill or outdoors. Supervision: The first three sessions are supervised in a laboratory setting. Subsequent sessions are unsupervised and performed at home with heart rate monitoring and remote data tracking via Polar Flow for Coach. |
|
No Intervention: Control
Keep the usual life style without intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
VO2max
Time Frame: Baseline (pre-intervention) and immediately after 6-week intervention completion
|
Progressive Aerobic Cardiovascular Endurance Run 20-m (measured in laps)
|
Baseline (pre-intervention) and immediately after 6-week intervention completion
|
|
Sleep Quality
Time Frame: Baseline (pre-intervention) and immediately after 6-week intervention completion
|
Pittsburgh Sleep Quality Index (PSQI) (scored from 0 to 21, with higher scores indicating worse sleep quality)
|
Baseline (pre-intervention) and immediately after 6-week intervention completion
|
|
Handgrip
Time Frame: Baseline (pre-intervention) and immediately after 6-week intervention completion
|
Handgrip dynamometer (measured in kilograms)
|
Baseline (pre-intervention) and immediately after 6-week intervention completion
|
|
Core strength
Time Frame: Baseline (pre-intervention) and immediately after 6-week intervention completion
|
Plank test (measured in second)
|
Baseline (pre-intervention) and immediately after 6-week intervention completion
|
|
Balance
Time Frame: Baseline (pre-intervention) and immediately after 6-week intervention completion
|
Unipedal stance test (measured in second)
|
Baseline (pre-intervention) and immediately after 6-week intervention completion
|
|
Agility
Time Frame: Baseline (pre-intervention) and immediately after 6-week intervention completion
|
Agility T-test (measured in second)
|
Baseline (pre-intervention) and immediately after 6-week intervention completion
|
|
Flexibility
Time Frame: Baseline (pre-intervention) and immediately after 6-week intervention completion
|
Sit and Reach Test
|
Baseline (pre-intervention) and immediately after 6-week intervention completion
|
|
Body composition (measured in centimeter)
Time Frame: Baseline (pre-intervention) and immediately after 6-week intervention completion
|
Bioelectrical impedance analysis (BIA) device (MC-780MA)
|
Baseline (pre-intervention) and immediately after 6-week intervention completion
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Carbohydrate Intake
Time Frame: Baseline (pre-intervention) and immediately after 6-week intervention completion
|
Daily carbohydrate consumption measured by validated 3-day food diary (measured in grams/day)
|
Baseline (pre-intervention) and immediately after 6-week intervention completion
|
|
Fat Intake
Time Frame: Baseline (pre-intervention) and immediately after 6-week intervention completion
|
Daily fat consumption measured by a validated 3-day food diary (measured in grams/day)
|
Baseline (pre-intervention) and immediately after 6-week intervention completion
|
|
Protein Intake
Time Frame: Baseline (pre-intervention) and immediately after 6-week intervention completion
|
Daily protein consumption measured by a validated 3-day food diary (measured in grams/day)
|
Baseline (pre-intervention) and immediately after 6-week intervention completion
|
|
Physical Activity Level
Time Frame: Baseline (pre-intervention) and immediately after 6-week intervention completion
|
International Physical Activity Questionnaire (IPAQ) long form (measured in MET-minutes/week, range: 0 to no upper limit, with higher scores indicating higher levels of physical activity)
|
Baseline (pre-intervention) and immediately after 6-week intervention completion
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Yano A, Hidaka E, Fujiwara K, Iimoto M. Induction of primary root curvature in radish seedlings in a static magnetic field. Bioelectromagnetics. 2001 Apr;22(3):194-9. doi: 10.1002/bem.38.
- Eather N, Riley N, Miller A, Smith V, Poole A, Vincze L, Morgan PJ, Lubans DR. Efficacy and feasibility of HIIT training for university students: The Uni-HIIT RCT. J Sci Med Sport. 2019 May;22(5):596-601. doi: 10.1016/j.jsams.2018.11.016. Epub 2018 Nov 24.
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 (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SBRE-23-0914
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
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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