Effect of Post-exercise Nutrition on Glycemia in Women

NCT ID: NCT05876260

Last Updated: 2024-05-07

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-05-24

Study Completion Date

2024-05-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to assess whether post-exercise Greek yogurt following a single session of aerobic exercise improves metabolic and musculoskeletal health in women with overweight/obesity.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Following the acquisition of informed consent, eligibility to participate in the study will be determined using questionnaires. Participants will undergo baseline testing at our laboratory at the University of Toronto to determine cardiorespiratory fitness, body composition and undergo exercise familiarization.

Eligible participants will be assigned, in a random order, to two metabolic trials approximately 4 weeks apart that involve 4 days of controlled diet and exercise. Each trial takes place over 4 days, but participants are not required to come to the laboratory on all days. The two trials involve: 1) Exercise + Greek Yogurt (GY) 2) Exercise + a carbohydrate-based study supplement (SS).

During the 4 day trials, participants consume controlled diets and the study supplements (GY and SS). On 1 of these days participants will perform exercise in our lab followed by the consumption of GY or SS. Various outcomes will be measured throughout the trial, including glycemic control (via continuous glucose monitoring), fat oxidation, appetite and health outcomes in blood samples.

Throughout the duration of the study, participants will be asked to maintain their habitual diet and physical activity patterns, and maintain their current body weight.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Overweight and Obesity

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

High-intensity interval exercise and post-exercise Greek yogurt (HIIE+GY)

Participants will consume greek yogurt following a single session of exercise

Group Type EXPERIMENTAL

Greek yogurt

Intervention Type BEHAVIORAL

Following 2 days of controlled diet, participants will consume greek yogurt following high-intensity interval exercise

Exercise

Intervention Type BEHAVIORAL

Following 2 days of controlled diet, participants will perform high-intensity interval exercise following an overnight fast

High-intensity interval exercise and post-exercise carbohydrate study supplement (HIIE +SS)

Participants will consume a carbohydrate-based study supplement following a single session of exercise

Group Type ACTIVE_COMPARATOR

Carbohydrate-based study supplement

Intervention Type BEHAVIORAL

Following 2 days of controlled diet, participants will consume a carbohydrate-based study supplement following high-intensity interval exercise

Exercise

Intervention Type BEHAVIORAL

Following 2 days of controlled diet, participants will perform high-intensity interval exercise following an overnight fast

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Greek yogurt

Following 2 days of controlled diet, participants will consume greek yogurt following high-intensity interval exercise

Intervention Type BEHAVIORAL

Carbohydrate-based study supplement

Following 2 days of controlled diet, participants will consume a carbohydrate-based study supplement following high-intensity interval exercise

Intervention Type BEHAVIORAL

Exercise

Following 2 days of controlled diet, participants will perform high-intensity interval exercise following an overnight fast

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* 18-45 yrs
* BMI ≥27 kg/m2
* Elevated waist circumference (≥88 cm)
* ≤2 structured exercise sessions/week
* Weight stable (within ± 2kg for at least 6 months)
* Experiencing regular natural menstrual cycles
* Non-smoker

Exclusion Criteria

* Allergy to dairy foods
* Diagnosed lactose intolerance or an aversion to foods provided during the study (e.g., post-exercise snacks)
* Previous history of cardiovascular or metabolic disease
* The use of medication for managing blood glucose or lipid metabolism
* Current use of oral contraceptives or use within the last 3 months
* Irregular menstrual cycles (\<21 days or \>35 days)
* Pregnant or lactating
* Recreational tobacco or cannabis use
* Inability to perform the study exercise protocols
* Actively engaging in a low-carbohydrate diet (e.g., ketogenic, Atkins).
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Toronto

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Jenna Gillen

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Jenna Gillen, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Toronto

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Jenna Gillen

Toronto, Ontario, Canada

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Canada

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

42756-3

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.