Bodyweight Interval Exercise in the Fed Versus Fasted State

NCT ID: NCT06240442

Last Updated: 2024-02-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-05-14

Study Completion Date

2021-08-30

Brief Summary

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The purpose of this study is to investigate the effects of a single session of at-home bodyweight interval exercise, performed in the fasted or fed state, on postprandial glycemic management, post-exercise fat oxidation, and overall perceptions of appetite in recreationally active females. This is a remote/online study and does not involve any visits to the laboratory.

Detailed Description

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Following the acquisition of informed consent via videoconferencing, eligibility to participate in the study will be determined using questionnaires. If inclusion criteria is met, participants will undergo virtual exercise familiarization by following a pre-recorded instructional video.

Eligible participants will be assigned, in a random order, to two metabolic trials at least 3 days apart in the follicular phase of the same menstrual cycle. These visits will be online with an investigator on videoconferencing. The two trials involve: 1) Exercise followed by breakfast; and 2) Breakfast followed by exercise.

Various outcomes will be measured throughout the metabolic trials including: blood sugar, fat oxidation and appetite. All research tools needed to acquire these methods will be delivered to participants' place of residence.

Conditions

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Exercise

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Fasted Exercise

Exercise followed by breakfast

Group Type EXPERIMENTAL

Fasted exercise

Intervention Type OTHER

Bodyweight interval exercise performed 5 minutes before the start of a mixed-macronutrient breakfast meal

Fed Exercise

Breakfast followed by exercise

Group Type EXPERIMENTAL

Fed exercise

Intervention Type OTHER

Bodyweight interval exercise performed 10 minutes after the start of consuming a mixed-macronutrient breakfast meal

Interventions

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Fasted exercise

Bodyweight interval exercise performed 5 minutes before the start of a mixed-macronutrient breakfast meal

Intervention Type OTHER

Fed exercise

Bodyweight interval exercise performed 10 minutes after the start of consuming a mixed-macronutrient breakfast meal

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Females 18-35 years
* Recreationally active (complete \<150 min of exercise 1-3 days per week) and not training for any specific sport
* Experiencing monthly menstrual periods (eumenorrheic)
* Are not currently on oral contraceptives, or are taking triphasic oral contraceptives
* Body mass index (BMI) ≥18.5 kg/m2 and ≤30 kg/m2
* Regular consumption of a breakfast meal (solid and liquid meals apply) most (≥ 4) days of the week
* Have a device compatible for use with study applications (e.g., smart phone)

Exclusion Criteria

* Inability to safely perform physical activity as determined by the Get Active Questionnaire
* Not willing to consume the standardized test drink before and after exercise
* Sensitive to meal timing around exercise (e.g., gastrointestinal issues if exercise performed 10 min after the start of meal consumption or if a meal is consumed 5 min after exercise)
* Inability to adhere to pre-trial protocol guidelines (e.g., caffeine or alcohol restrictions)
* Physical limitations for bodyweight exercise
* Are on monophasic or biphasic oral contraceptives
* Regular tobacco or cannabis use (e.g., recreational and/or medical cannabis, cigarettes, e-cigarettes, vape pens, JUUL)
* Regular use of drugs that may alter metabolism (e.g., corticosteroids, nSAIDs)
* Diagnosed medical condition under the care of care of a physician (e.g., type 2 diabetes, cardiovascular disease) Currently enrolled in a course with Dr. Gillen
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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University of Toronto

OTHER

Sponsor Role lead

Responsible Party

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Jenna Gillen

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jenna Gillen, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Toronto

Locations

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Goldring Centre for High Performance Sport

Toronto, Ontario, Canada

Site Status

Countries

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Canada

Other Identifiers

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40799

Identifier Type: -

Identifier Source: org_study_id

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