- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04437550
Effects of Exercise Intensity on Energy Intake, Appetite and Enjoyment in Overweight and Obese Females
Interval exercise involves short bouts of high intensity exercise interspersed with periods of lower intensity exercise. The benefit is that a shorter total duration of exercise may be required to achieve cardiovascular benefits similar to or even superior to traditional longer bouts of steady state endurance exercise. However how this type of exercise affects appetite and energy intake, particularly in overweight and obese females is not well known.
This study involves two trials of exercise, one at high intensity and one at low intensity, followed by a buffet lunch, in overweight and obese females.
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Pennsylvania
-
Scranton, Pennsylvania, United States, 18509
- Human Physiology Lab
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Female
- Adult
- apparently healthy
- overweight or class I obese
- eumenorrheic
Exclusion Criteria:
- Diabetes
- pregnancy
- cardiovascular disease
- greater than 1 hour of structured physical activity per week
- thyroid disease
- polycystic ovary disease
Study Plan
How is the study designed?
Design Details
- Primary Purpose: BASIC_SCIENCE
- Allocation: RANDOMIZED
- Interventional Model: CROSSOVER
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: high-intensity
|
high intensity exercise = 15 x 60 s sprints at 85% velocity of VO2max (vVO2max) with 60 s walking at 20% vVO2max or moderate intensity exercise = walking at 60% vVO2max
|
|
EXPERIMENTAL: low-intensity
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high intensity exercise = 15 x 60 s sprints at 85% velocity of VO2max (vVO2max) with 60 s walking at 20% vVO2max or moderate intensity exercise = walking at 60% vVO2max
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in energy expenditure
Time Frame: immediately pre-breakfast, immediately pre-exercise, during exercise, and immediately post-exercise.
|
caloric expenditure measured via indirect calorimetry
|
immediately pre-breakfast, immediately pre-exercise, during exercise, and immediately post-exercise.
|
|
Change in energy intake
Time Frame: immediately post exercise
|
measured via standardized lunch
|
immediately post exercise
|
|
Change in appetite
Time Frame: immediately pre-breakfast, immediately post-breakfast, immediately post-exercise and immediately pre-lunch
|
measured via circulating hormones leptin and acylated ghrelin
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immediately pre-breakfast, immediately post-breakfast, immediately post-exercise and immediately pre-lunch
|
|
Change in subjective hunger
Time Frame: baseline, immediately pre-exercise, immediately post-exercise, immediately pre-lunch, and immediately post-lunch
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via visual analogue scale 100 mm, higher scores indicate greater hunger
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baseline, immediately pre-exercise, immediately post-exercise, immediately pre-lunch, and immediately post-lunch
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 801776
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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