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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07256847
Enrollment
56
Registered
2025-12-01
Start date
2024-07-01
Completion date
2025-01-31
Last updated
2025-12-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sedentary Students, University Students

Brief summary

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.

Interventions

OTHERHigh intensity interval training

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.

Sponsors

Ma Ruisi
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Body composition (measured in centimeter)Baseline (pre-intervention) and immediately after 6-week intervention completionBioelectrical impedance analysis (BIA) device (MC-780MA)
Core strengthBaseline (pre-intervention) and immediately after 6-week intervention completionPlank test (measured in second)
BalanceBaseline (pre-intervention) and immediately after 6-week intervention completionUnipedal stance test (measured in second)
AgilityBaseline (pre-intervention) and immediately after 6-week intervention completionAgility T-test (measured in second)
FlexibilityBaseline (pre-intervention) and immediately after 6-week intervention completionSit and Reach Test
VO2maxBaseline (pre-intervention) and immediately after 6-week intervention completionProgressive Aerobic Cardiovascular Endurance Run 20-m (measured in laps)
Sleep QualityBaseline (pre-intervention) and immediately after 6-week intervention completionPittsburgh Sleep Quality Index (PSQI) (scored from 0 to 21, with higher scores indicating worse sleep quality)
HandgripBaseline (pre-intervention) and immediately after 6-week intervention completionHandgrip dynamometer (measured in kilograms)

Other

MeasureTime frameDescription
Fat IntakeBaseline (pre-intervention) and immediately after 6-week intervention completionDaily fat consumption measured by a validated 3-day food diary (measured in grams/day)
Protein IntakeBaseline (pre-intervention) and immediately after 6-week intervention completionDaily protein consumption measured by a validated 3-day food diary (measured in grams/day)
Physical Activity LevelBaseline (pre-intervention) and immediately after 6-week intervention completionInternational 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)
Carbohydrate IntakeBaseline (pre-intervention) and immediately after 6-week intervention completionDaily carbohydrate consumption measured by validated 3-day food diary (measured in grams/day)

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026