High-Intensity Interval Training and Fat Mass Losses (RIESLING)
Primary Purpose
Overweight and Obesity, Men
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Physical activity
Sponsored by

About this trial
This is an interventional treatment trial for Overweight and Obesity focused on measuring cycling, running, high-intensity interval training, fat mass, visceral tissue, health
Eligibility Criteria
Inclusion Criteria:
- men (18 to 65 years old)
- with overweight or obesity (BMI > 25 kg/m2 and ≤ 40 kg/m2)
Exclusion Criteria:
- medical contraindications to intense physical activity,
- painful joints,
- taking ß-blocker
Sites / Locations
- CREPS Auvergne Rhône-Alpes / Vichy
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
High intensity interval training - BIKE (HIIE BIKE)
High intensity interval training - RUN (HIIE RUN)
Arm Description
10 cycles of speeding up for 45 s at 80-thPHR followed by pedaling slowly (40% thPHR) for 1m30s (37min30s)
9 cycles of speeding up for 45 s at 80-thPHR followed by pedaling slowly (40% thPHR) for 1m30s (35min15s)
Outcomes
Primary Outcome Measures
HIIT mode and fat mass change (g)
change of total fat mass (in grams from DXA analysis) after 3 months of training- HIIT mode comparison
HIIT mode and abdominal fat mass change (g)
change of abdominal fat mass (in grams from DXA analysis) after 3 months of training- HIIT mode comparison
Secondary Outcome Measures
Rate of carbohydrate and lipid oxidation (g.min-1) during a sub-maximal exercise by measuring gaz exchange.
Carbohydrate and lipid oxidation rate (g.min-1) during a submaximal exercise before and after the HIIT protocol. HIIT mode comparison.
Full Information
NCT ID
NCT05311800
First Posted
March 16, 2022
Last Updated
February 22, 2023
Sponsor
Laboratoire des Adaptations Métaboliques à l'Exercice en conditions Physiologiques et Pathologiques
1. Study Identification
Unique Protocol Identification Number
NCT05311800
Brief Title
High-Intensity Interval Training and Fat Mass Losses
Acronym
RIESLING
Official Title
Effect of Two Isoenergetic Modes of High-Intensity Interval Training on Total and Abdominal Fat Mass Loss in Men With Overweight or Obesity.
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
September 1, 2021 (Actual)
Primary Completion Date
July 1, 2022 (Actual)
Study Completion Date
July 1, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Laboratoire des Adaptations Métaboliques à l'Exercice en conditions Physiologiques et Pathologiques
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aims of this study was to compare two isoenergetic HIIT (High-intensity Interval training) programs (cycling vs. running) on body composition, substrate oxidation at rest and during a moderate exercise, muscle functionality, glycaemic control, lipid profile, inflammation, maximal aerobic capacity (VO2max) and gut microbiota composition in men with overweight or obesity.
The investigators hypothesized that both programs could decrease total, abdominal and visceral fat mass but due to differences in muscle solicitation, metabolism adaptation and blood flow, and that running could favors greater fat mass losses.
Detailed Description
The first aim of this study was to compare two isoenergetic HIIT programs (cycling vs. running) on body composition in men with overweight or obesity.
20 men with overweight or obesity should completed HIIT program three times a week during twelve weeks.
i) High intensity interval training - BIKE (HIIE BIKE) 10 cycles of speeding up for 45 s at 80-thPHR followed by pedaling slowly (40% thPHR) for 1m30s (37min30s) ii) High intensity interval training - RUN (HIIE RUN) 9 cycles of speeding up for 45 s at 80-thPHR followed by pedaling slowly (40% thPHR) for 1m30s (35min15s)
Body composition will be measured before and after HIIT program by Dual-energy X-ray absorptiometry (DXA).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight and Obesity, Men
Keywords
cycling, running, high-intensity interval training, fat mass, visceral tissue, health
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
2 groups : running vs cycling
Masking
Participant
Masking Description
Data collected on the volunteers will be made anonymous.
Allocation
Randomized
Enrollment
9 (Actual)
8. Arms, Groups, and Interventions
Arm Title
High intensity interval training - BIKE (HIIE BIKE)
Arm Type
Experimental
Arm Description
10 cycles of speeding up for 45 s at 80-thPHR followed by pedaling slowly (40% thPHR) for 1m30s (37min30s)
Arm Title
High intensity interval training - RUN (HIIE RUN)
Arm Type
Experimental
Arm Description
9 cycles of speeding up for 45 s at 80-thPHR followed by pedaling slowly (40% thPHR) for 1m30s (35min15s)
Intervention Type
Other
Intervention Name(s)
Physical activity
Intervention Description
Comparison of HIIT mode (running vs cycling)
Primary Outcome Measure Information:
Title
HIIT mode and fat mass change (g)
Description
change of total fat mass (in grams from DXA analysis) after 3 months of training- HIIT mode comparison
Time Frame
At the first and the last training - week 1 and 12
Title
HIIT mode and abdominal fat mass change (g)
Description
change of abdominal fat mass (in grams from DXA analysis) after 3 months of training- HIIT mode comparison
Time Frame
At the first and the last training - week 1 and 12
Secondary Outcome Measure Information:
Title
Rate of carbohydrate and lipid oxidation (g.min-1) during a sub-maximal exercise by measuring gaz exchange.
Description
Carbohydrate and lipid oxidation rate (g.min-1) during a submaximal exercise before and after the HIIT protocol. HIIT mode comparison.
Time Frame
At the first and the last training - week 1 and 12
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
men (18 to 65 years old)
with overweight or obesity (BMI > 25 kg/m2 and ≤ 40 kg/m2)
Exclusion Criteria:
medical contraindications to intense physical activity,
painful joints,
taking ß-blocker
Facility Information:
Facility Name
CREPS Auvergne Rhône-Alpes / Vichy
City
Bellerive-sur-Allier
State/Province
Allier
ZIP/Postal Code
03321
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
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High-Intensity Interval Training and Fat Mass Losses
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