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Acute and Chronic Metabolic Flexibility in Individuals Living With Obesity: The i-FLEX Study

Sprint Interval Training: Insulin Sensitivity and Acute-Chronic Metabolic Flexibility in Individuals Living With Obesity: The i-FLEX Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03527446
Acronym
i-FLEX
Enrollment
34
Registered
2018-05-17
Start date
2018-07-03
Completion date
2020-02-28
Last updated
2020-03-25

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

Conditions

Exercise, Insulin Sensitivity, Obesity, Obesity; Endocrine

Keywords

Metabolic flexibility, Insulin sensitivity, Sprint interval training, Obesity, Exercise intensity

Brief summary

Regular exercise is a cornerstone in the prevention and the management of cardio-metabolic risk factors. Some of the beneficial effect of exercise training occurs through metabolic flexibility' enhancement. Metabolic flexibility is the ability to respond or adapt to conditional changes in metabolic demand, and previous literature has shown that individuals living with obesity have an impaired metabolic flexibility compared to lean individuals. However, there is a lack of empirical evidence on the impact of sprint interval training on metabolic flexibility and whether this translates into clinically meaningful outcomes. This study will evaluate the impact of 4-week sprint interval training in normal weight individuals as well as individuals living with obesity on acute and chronic metabolic flexibility, irisin secretion and insulin sensitivity.

Interventions

The 4-week sprint interval intervention will consist of a work-rest ratio of four 30-s intervals of exercise at maximal capacity and 4-min of passive recovery at 50% of maximal capacity between intervals. There will be three sessions per week.

Sponsors

University of New Brunswick
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Individuals living with obesity (BMI ≥ 30 km/m2; n=15) as well as normal weight (BMI ≥ 18.5 \< 25.0 km/m2; n=15) adults (aged between 19 to 60 years) will be recruited to participate in the study. All participants will be asked to come in for a total of two visits and participate in a 4-week intervention.

Eligibility

Sex/Gender
ALL
Age
19 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Adults (Ages 19-60) * Physically inactive for individuals living with obesity (not meeting Canadian Physical Activity Guidelines) * Normal Weight (BMI ≥ 18.5 \< 25.0 km/m2) * Obesity (BMI ≥ 30.0 km/m2)

Exclusion criteria

* Individuals with Type 2 Diabetes. * Individuals with impaired glucose tolerance. * Individuals living with obesity that partake in regular exercise training / meet the Canadian Physical Activity Guidelines. * Individuals with a condition or injury that may impact the ability to perform exercise or may be worsened by exercise. * Individuals currently being treated with corticosteroids or atypical antipsychotics, as these agents significantly influence carbohydrate metabolism. * have experienced \>10% weight loss or enrolled in weight loss program within six months of enrolment. * require use of medication(s) known to affect insulin sensitivity or secretion within the last 30 days. * Medication(s) known to cause weight gain. * weight loss medication(s).

Design outcomes

Primary

MeasureTime frameDescription
Change in Metabolic FlexibilityBaseline and post-intervention (4 weeks)Chronic and acute metabolic flexibility will be quantified from the respiratory quotient (RQ) at rest and from the respiratory exchange ratio (RER) during a 4-6 minutes steady rate exercise bout.
Change in Insulin SensitivityBaseline and post-intervention (4 weeks)Insulin sensitivity will be measure with the Matsuda Index

Secondary

MeasureTime frameDescription
Change in IrisinBaseline and post-intervention (4 weeks)This hormone will be quantified in the plasma during one acute session of exercise.

Countries

Canada

Outcome results

None listed

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