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Can Brief High-intensity Interval Training Mitigate the Adverse Consequences of High-fat Overfeeding?

Can Brief High-intensity Interval Training Mitigate the Adverse Consequences of High-fat Overfeeding?

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02177604
Acronym
GAINHIT
Enrollment
7
Registered
2014-06-27
Start date
2014-11-30
Completion date
2016-12-31
Last updated
2018-05-25

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

Conditions

Insulin Resistance

Brief summary

Previous research has shown that indulging in 50% more calories than required for as little as 3 days can significantly impact markers of metabolic health in lean and overweight individuals. Here, the investigators will determine if 3 brief sessions of high-intensity interval training can mitigate the adverse consequences of 7 days high-fat overfeeding in sedentary, overweight males.

Interventions

OTHERWingate HIT

3 sessions of Wingate based High-Intensity Interval Training (6-8 x 15 second all out sprints on a cycle ergometer interspersed by 2 minutes recovery)

OTHERModified HIT

3 sessions of Modified High-Intensity Interval Training (8 x 60 second sprints at approximately 90-95% VO2 peak on a cycle ergometer interspersed by 60 seconds recovery)

7 days of high-fat overfeeding (50% excess calories)

Sponsors

Royal Adelaide Hospital
CollaboratorOTHER
University of South Australia
CollaboratorOTHER
University of Adelaide
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* Sedentary (no more than 2 sessions of structured moderate intensity aerobic exercise or resistance training per week) * Overweight (BMI 25-29.9 kg/m2)

Exclusion criteria

* Personal history of any major illness (i.e. cardiovascular disease, diabetes, hypertension, cancer, renal/liver impairments, major psychiatric disorders, eating disorders etc.) * History of chest pain (either at rest or during exercise.) * Abnormal resting ECG at screening visit * Chronic use of any prescribed or non-prescribed medications (i.e. anti-hypertensive, statins, metformin, anti-inflammatories, antidepressants etc.) * Blood pressure or blood lipids outside of reference ranges * Serum ferritin \<30ng/mL * Uncontrolled asthma, current fever, or upper respiratory infection * Current intake of \> 140g alcohol/week * Current smokers of cigarettes/cigars/marijuana * Current intake of any illicit substance * Experience claustrophobia in confined spaces * Donated blood in the past 3 months * Migraines * Unable to comprehend study protocol * Unable to perform exercise on a cycle ergometer at second screening visit

Design outcomes

Primary

MeasureTime frameDescription
Change in glucose metabolism1 weekChanges in insulin and glucose area under the curve assessed via 75g Oral Glucose Tolerance Test.

Secondary

MeasureTime frameDescription
Change in plasma levels of cytokines1 weekChange in plasma levels of adiponectin, irisin, sex hormone-binding globulin and c-reactive protein

Other

MeasureTime frameDescription
Change in mitochondrial metabolism1 weekChanges in citrate synthase activity, mitochondrial DNA content and protein levels of PGC-1a
Change in resting energy expenditure1 weekChanges in resting energy expenditure measured by metabolic cart
Change in cognitive function1 weekChanges in cognitive function, assessed by a series of computer tasks involving vigilant attention and speed processing.

Countries

Australia

Outcome results

None listed

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