Effects of Different Sports Supplements on Metabolism and Perceptual Responses During Distance Running

NCT ID: NCT03596788

Last Updated: 2025-03-20

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

TERMINATED

Clinical Phase

NA

Total Enrollment

4 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-08-01

Study Completion Date

2025-02-17

Brief Summary

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

Several previous studies have shown that repeatedly ingesting carbohydrate supplements during exercise training sessions, over a period of days and weeks, can gradually increase carbohydrate oxidation and reduce gut discomfort during exercise. However, repeatedly ingesting large amounts of carbohydrate during training sessions can be burdensome and can cause gut distress. Thus, it would be advantageous if the same long-term benefits could be realized from consuming these carbohydrate supplements at rest instead of specifically during training sessions. Therefore, the goal of this study is to examine whether repeatedly ingesting a carbohydrate-rich beverage at rest over a 5-day period alters metabolism and gut symptoms while ingesting carbohydrate during exercise.

Detailed Description

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

Conditions

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

Anomalies Gastrointestinal

Study Design

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

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants

Study Groups

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

Carbohydrate Beverage

A glucose-fructose beverage mixture supplying 100 grams of carbohydrate per day for 5 days

Group Type EXPERIMENTAL

Carbohydrate Beverage

Intervention Type DIETARY_SUPPLEMENT

The carbohydrate beverage will supply approximately 100 grams of carbohydrate per day (in the form of glucose and fructose)

Placebo Beverage

An artificially-sweetened beverage containing aspartame

Group Type PLACEBO_COMPARATOR

Placebo Beverage

Intervention Type DIETARY_SUPPLEMENT

The placebo beverage will contain aspartame.

Interventions

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

Carbohydrate Beverage

The carbohydrate beverage will supply approximately 100 grams of carbohydrate per day (in the form of glucose and fructose)

Intervention Type DIETARY_SUPPLEMENT

Placebo Beverage

The placebo beverage will contain aspartame.

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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

Inclusion Criteria

* Be currently running ≥15 miles per week
* Have completed at least one run \>60 minutes over the past month
* Have completed one or more marathons within the past year

Exclusion Criteria

* Overt cardiovascular disease or metabolic disorder
* Adverse symptoms (e.g., unusual shortness of breath, dizziness, chest pain) with exercise
* Allergies/intolerances to any of the ingredients in the beverages
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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

Old Dominion University

OTHER

Sponsor Role lead

Responsible Party

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

Patrick Wilson, PhD

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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

Patrick Wilson, PhD

Role: PRINCIPAL_INVESTIGATOR

Old Dominion University

Locations

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

Human Performance Lab

Norfolk, Virginia, United States

Site Status

Countries

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

United States

Other Identifiers

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

1223706-2

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

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

Carbohydrate Mouth-rinse
NCT01527266 UNKNOWN NA