Carbohydrate Mouth Rinsing and Cognitive Response During Exercise

NCT ID: NCT07099807

Last Updated: 2025-08-01

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

11 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-02-28

Study Completion Date

2025-05-17

Brief Summary

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This study investigates whether rinsing the mouth with a carbohydrate solution can improve brain oxygenation and cognitive function during high-intensity exercise. Eleven trained cyclists participated in multiple exercise sessions under different mouth rinse conditions. Brain oxygenation, perceived exertion, and cognitive performance were measured. The goal is to understand if this simple technique can support both physical and mental performance during demanding exercise.

Detailed Description

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Conditions

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Exercise Performance of Fit Athletes

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Carbohydrate Mouth Rinse

Group Type EXPERIMENTAL

Carbohydrate Mouth Rinse

Intervention Type BEHAVIORAL

A 6.4% maltodextrin solution (64 g/L) was prepared using Nutricost Maltodextrin Powder. Participants performed five mouth rinses per trial, each using 25 mL of the solution for 10 seconds before expectorating. Each rinse was followed by a 30-second rest. Participants were instructed not to swallow the solution. Rinsing procedure was standardized across all sessions.

Placebo Mouth Rinse

Group Type PLACEBO_COMPARATOR

Placebo Mouth Rinse

Intervention Type BEHAVIORAL

A placebo solution containing 0.05 g/L of non-caloric sucralose in distilled water was used to match sweetness and viscosity of the CHO-MR. Participants performed five rinses of 25 mL for 10 seconds each, spitting out the solution after each rinse. 30-second rest intervals followed each rinse. Swallowing was not allowed. Rinse frequency, volume, and duration were standardized.

Music Listening

Group Type EXPERIMENTAL

Music Listening

Intervention Type BEHAVIORAL

Participants listened to high-tempo music (120 bpm) for 15 minutes before exercise using standardized earbuds. Music was selected from a public YouTube playlist titled "120 BPM Best Dance Music for Running and Working Out." Volume was calibrated at 65 dB (50% of max device volume). Auditory conditions were standardized across all participants.

Interventions

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Carbohydrate Mouth Rinse

A 6.4% maltodextrin solution (64 g/L) was prepared using Nutricost Maltodextrin Powder. Participants performed five mouth rinses per trial, each using 25 mL of the solution for 10 seconds before expectorating. Each rinse was followed by a 30-second rest. Participants were instructed not to swallow the solution. Rinsing procedure was standardized across all sessions.

Intervention Type BEHAVIORAL

Placebo Mouth Rinse

A placebo solution containing 0.05 g/L of non-caloric sucralose in distilled water was used to match sweetness and viscosity of the CHO-MR. Participants performed five rinses of 25 mL for 10 seconds each, spitting out the solution after each rinse. 30-second rest intervals followed each rinse. Swallowing was not allowed. Rinse frequency, volume, and duration were standardized.

Intervention Type BEHAVIORAL

Music Listening

Participants listened to high-tempo music (120 bpm) for 15 minutes before exercise using standardized earbuds. Music was selected from a public YouTube playlist titled "120 BPM Best Dance Music for Running and Working Out." Volume was calibrated at 65 dB (50% of max device volume). Auditory conditions were standardized across all participants.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Aged between 20 and 30 years
* Engaged in regular cycling training (≥5 sessions per week, \~4 hours per day)
* No known cardiovascular, neurological, or metabolic diseases
* Provided written informed consent

Exclusion Criteria

* Current use of medication affecting cardiovascular or cognitive function
* Recent musculoskeletal injuries that affect cycling ability
* Smoking or excessive alcohol consumption
* Refusal or inability to comply with study procedures
Minimum Eligible Age

20 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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CHA University

OTHER

Sponsor Role lead

Responsible Party

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Park Seung-Bo

CHA Bundang Medical Center

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Seung-Bo Park

Role: PRINCIPAL_INVESTIGATOR

CHA University

Locations

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CHA University, Human Performance Lab

Seongnam-si, Gyeonggi-do, South Korea

Site Status

Countries

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South Korea

Other Identifiers

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Parks0524

Identifier Type: -

Identifier Source: org_study_id

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