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High-intensity interval training for health and fitness in males with overweight or obesity.

High-intensity interval training for health and fitness in males with overweight or obesity.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619001409167
Enrollment
28
Registered
2019-10-15
Start date
2016-07-01
Completion date
2017-09-30
Last updated
2019-10-22

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

Conditions

None listed

Brief summary

We compared the effectiveness of high-intensity interval training (HIIT) and moderate-intensity continuous training (MICT) on a range of health and fitness measures in males with overweight or obesity. Participants completed 6 weeks x 3 sessions per week training, randomised to either group. We hypothesised that HIIT and MICT would increase aerobic fitness, reduce body fat, blood pressure and pressure pain sensitivity, and improve mood state after 6 weeks of training, with greater effectiveness following HIIT compared to MICT.

Interventions

High-intensity interval training (HIIT) - randomized trial with moderate-intensity continuous training (MICT) acting as the comparator group to HIIT. Participants were randomly assigned (1:1) to a HIIT or MICT training group. - Exercise training sessions conducted over 6 weeks x 3 sessions per week. - all training conducted at a single site (university exercise research lab) where both groups trained in parallel. HIIT protocol details: Participants trained 3 times per week for 6 weeks. A mi

High-intensity interval training (HIIT) - randomized trial with moderate-intensity continuous training (MICT) acting as the comparator group to HIIT. Participants were randomly assigned (1:1) to a HIIT or MICT training group. - Exercise training sessions conducted over 6 weeks x 3 sessions per week. - all training conducted at a single site (university exercise research lab) where both groups trained in parallel. HIIT protocol details: Participants trained 3 times per week for 6 weeks. A minimum of 24 hours between training sessions was required and no more than two consecutive days of training. All training was conducted on manual-resistance cycle ergometers (Monark 828E Sweden) or electronically-braked cycle ergometers (Monark 928E; for HIIT participants only due to its ability to pre-programme interval training sessions). All sessions were supervised by trained research assistants (undergraduate Exercise Physiology students). Heart rate (HR) and rating of perceived exertion (RPE) were monitored throughout every training session using a Polar T34 heart rate monitor and unmodified (6-20) Borg scale 20 respectively. For HIIT participants, HR and RPE were recorded at the end of every 2nd interval and recovery period. HIIT sessions consisted of 10 × 1-minute intervals at 90-100% Wmax (approximating ~90% HRmax; RPE ~15), interspersed with 1 minute of active recovery at 15% Wmax. The intensity of training was progressively increased over the 6-week intervention (weeks 1 and 2: 90% Wmax; weeks 3 and 4: 95% Wmax; weeks 5 and 6: 100% Wmax). Each session began with a 3-minute warm-up at 35% Wmax (approximating 65% HRmax) and ended with a 2-minute cool down at 15% Wmax. Total exercising time for each session was 24 minutes for the HIIT group. Adherence was assessed by number of sessions attended. Compliance was assessed by monitoring HR in relation to desired HR target range for each session. Safety was assessed by reports of adverse events during or within 4 hours following each session.

Sponsors

UNSW
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
Male
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

Males aged 18-45, BMI 25-35 kg/m2, physically inactive

Exclusion criteria

diagnosed cardiovascular risk factors such as hypertension, diabetes or hyperlipidaemia; previous history of cardiovascular disease; or any uncontrolled medical disorder

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026