Effect of 6-Week High Intensity Interval Training on VO2max, Physical Competence and Sleep Quality in Sedentary Male University Students

November 20, 2025 updated by: Ma Ruisi
This study aims to investigate the effects of a 6-week high-intensity interval training (HIIT) intervention on physical fitness, cardiorespiratory capacity (VO2max), and sleep quality among sedentary male college students. Through a randomized controlled trial, we seek to examine whether HIIT, as a time-efficient exercise modality, can effectively improve these health-related outcomes in young adults who maintain predominantly sedentary lifestyles. This research will provide evidence-based insights into the effectiveness of HIIT as a potential intervention strategy to address the physical and physiological consequences of prolonged sitting behavior among university students.

Study Overview

Status

Completed

Study Type

Interventional

Enrollment (Actual)

56

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

    • None Selected
      • Hong Kong, None Selected, Hong Kong
        • SSPE, The Chinese University of Hong Kong

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
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. university students;
  2. daily sedentary time > 8 hours;
  3. healthy individuals who are capable of physical tests or HIIT;
  4. no regular exercise habits;
  5. can understand English or Chinese.

Exclusion Criteria:

  1. self-reported history of neurological, psychiatric, or medical diseases;
  2. current intake of medications and/or recreational drugs that could affect the central nervous system and/or the ability to learn.

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: 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

This is where you will find people and organizations involved with this study.

Sponsor

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)

July 1, 2024

Primary Completion (Actual)

December 31, 2024

Study Completion (Actual)

January 31, 2025

Study Registration Dates

First Submitted

November 20, 2025

First Submitted That Met QC Criteria

November 20, 2025

First Posted (Actual)

December 1, 2025

Study Record Updates

Last Update Posted (Actual)

December 1, 2025

Last Update Submitted That Met QC Criteria

November 20, 2025

Last Verified

July 1, 2024

More Information

Terms related to this study

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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