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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05226962
Other study ID # 13837
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 15, 2022
Est. completion date October 1, 2022

Study information

Verified date November 2022
Source McMaster University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Diet can alter blood ketone levels and this in turn may affect exercise capacity. This study will determine if the acute ingestion of a ketone supplement alters cycling time trial performance. Participants will perform two trials in a randomized order. Each trial will involve a 20-minute bout of cycling on a stationary ergometer. Participants will ingest either a ketone supplement or a taste-matched placebo drink prior to exercise. Blood samples will be obtained to assess selected metabolic responses. This study will provide information regarding the effect of ketone supplementation on exercise responses.


Description:

This study will determine if the acute ingestion of a ketone supplement alters cycling time trial performance. Trained participants with competitive cycling experience will be recruited. Exercise will involve a 20-minute bout of cycling on a stationary ergometer with the goal of producing the highest power output possible. Participants will ingest either a ketone supplement or a taste-matched placebo drink prior to exercise using a randomized, double-blind crossover design. Diet prior to exercise will be standardized between trials for a given participant. Blood samples will be obtained to assess selected metabolic responses. This study will provide information regarding the effect of ketone supplementation on exercise responses.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date October 1, 2022
Est. primary completion date September 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Habitually ingesting >50 g of dietary carbohydrate daily i.e. not following a ketogenic diet. - Regularly performing cycling exercise at least 3 days per week and for a total of =5 hours per week. - Having an estimated peak oxygen uptake of =55 ml/kg/min for males and =48 ml/kg/min for females based on the online fitness calculator available at: www.worldfitnesslevel.org. - Having competitive cycling experience. Exclusion Criteria: - Experiencing a condition that might preclude safe participation in physical activity and exercise, as determined by answering "Yes" to any question on Page 1 of the Canadian Society for Exercise Physiology Get Active Questionnaire.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Ketone monoester
A commercial liquid supplement ingested in a dose intended to provide ~0.35 g of ketone monoester per kg body mass of the participant
Other:
Placebo
A liquid placebo that is volume- and taste-matched to the ketone monoester supplement

Locations

Country Name City State
Canada McMaster University Hamilton Ontario

Sponsors (1)

Lead Sponsor Collaborator
McMaster University

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Power output Mean power output produced while cycling 20-minute measurement during exercise
Secondary Heart rate Mean heart rate while cycling 20-minute measurement during exercise
Secondary Perceived exertion Rating of perceived exertion while cycling Single measurement immediately after exercise
Secondary Blood ketone Blood ketone before exercise Single measurement immediately prior to exercise
Secondary Blood glucose Mean blood glucose while cycling 20-minute measurement during exercise
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