Effects of Exercise Intensity on Energy Intake, Appetite and Enjoyment in Overweight and Obese Females

June 16, 2020 updated by: Angela Hillman, Ohio University

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

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

11

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Pennsylvania
      • Scranton, Pennsylvania, United States, 18509
        • Human Physiology Lab

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 45 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  1. Female
  2. Adult
  3. apparently healthy
  4. overweight or class I obese
  5. eumenorrheic

Exclusion Criteria:

  1. Diabetes
  2. pregnancy
  3. cardiovascular disease
  4. greater than 1 hour of structured physical activity per week
  5. thyroid disease
  6. polycystic ovary disease

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
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
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
via visual analogue scale 100 mm, higher scores indicate greater hunger
baseline, immediately pre-exercise, immediately post-exercise, immediately pre-lunch, and immediately post-lunch

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Collaborators

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

January 1, 2016

Primary Completion (ACTUAL)

June 1, 2016

Study Completion (ACTUAL)

August 1, 2016

Study Registration Dates

First Submitted

June 15, 2020

First Submitted That Met QC Criteria

June 16, 2020

First Posted (ACTUAL)

June 18, 2020

Study Record Updates

Last Update Posted (ACTUAL)

June 18, 2020

Last Update Submitted That Met QC Criteria

June 16, 2020

Last Verified

June 1, 2020

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)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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