Opti-MCT: Acute Medium Chain Triglycerides (MCT) Intake in Young and Older Participants

Sponsor
Université de Sherbrooke (Other)
Overall Status
Completed
CT.gov ID
NCT03830268
Collaborator
(none)
20
1
2
24.7
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Study Details

Study Description

Brief Summary

Compare plasma metabolites following different conditions paired with a dietary MCT beverage over an 8-hour metabolic day protocol in young and older participants.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: No MCT intake with breakfast, no lunch
  • Dietary Supplement: No MCT intake with lunch, no breakfast
  • Dietary Supplement: 10g of Betaquik
  • Dietary Supplement: 10g of Betaquik with low-carbs breakfast
  • Dietary Supplement: 20g of Betaquik
  • Dietary Supplement: 10g of Betaquik with lunch, no breakfast
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
20 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
10 young and 10 older participants undergoing six separate but identical metabolic visits (interventions)10 young and 10 older participants undergoing six separate but identical metabolic visits (interventions)
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Optimisation of Acute Medium Chain Triglycerides Intake Characteristics on Different Plasma Metabolites in Young and Older Participants
Actual Study Start Date :
Jun 2, 2017
Actual Primary Completion Date :
Jun 25, 2019
Actual Study Completion Date :
Jun 25, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: MCT intake in young participants

Different conditions paired with a dietary MCT beverage over an 8-hour metabolic day protocol in young participants. Interventions: No MCT intake with breakfast, no lunch (i.e. CTL) No MCT intake with lunch, no breakfast (i.e CTL inverted) 10g of Betaquik with breakfast, no lunch (i.e BQ10) 20g of Betaquik with breakfast, no lunch (i.e BQ20) 10g of Betaquik with low-carbs breakfast, no lunch (i.e BQ10LC) 10g of Betaquik with lunch, no breakfast (i.e BQ10 inverted)

Dietary Supplement: No MCT intake with breakfast, no lunch
Water given with a regular standardize breakfast and water given at noon without lunch.
Other Names:
  • CTL
  • Dietary Supplement: No MCT intake with lunch, no breakfast
    Water given in the beginning of the metabolic study day without breakfast and water given at noon with a regular standardize lunch.
    Other Names:
  • CTL inverted
  • Dietary Supplement: 10g of Betaquik
    BQ10 given with a regular standardize breakfast and BQ10 given at noon without lunch.
    Other Names:
  • BQ10
  • Dietary Supplement: 10g of Betaquik with low-carbs breakfast
    BQ10 given with a low-carbs standardize breakfast and BQ10 given at noon without lunch.
    Other Names:
  • BQ10LC
  • Dietary Supplement: 20g of Betaquik
    BQ20 given with a regular standardize breakfast and BQ20 given at noon without lunch.
    Other Names:
  • BQ20
  • Dietary Supplement: 10g of Betaquik with lunch, no breakfast
    BQ10 given in the beginning of the metabolic study day without breakfast and BQ10 given at noon with a regular standardize lunch.
    Other Names:
  • BQ10 inverted
  • Experimental: MCT intake in older participants

    Different conditions paired with a dietary MCT beverage over an 8-hour metabolic day protocol in older participants. Interventions: No MCT intake with breakfast, no lunch (i.e. CTL) No MCT intake with lunch, no breakfast (i.e CTL inverted) 10g of Betaquik with breakfast, no lunch (i.e BQ10) 20g of Betaquik with breakfast, no lunch (i.e BQ20) 10g of Betaquik with low-carbs breakfast, no lunch (i.e BQ10LC) 10g of Betaquik with lunch, no breakfast (i.e BQ10 inverted)

    Dietary Supplement: 10g of Betaquik
    BQ10 given with a regular standardize breakfast and BQ10 given at noon without lunch.
    Other Names:
  • BQ10
  • Outcome Measures

    Primary Outcome Measures

    1. Concentration of plasma ketones (acetoacetate and B-hydroxybutyrate) [8 hours]

      To compare acute ketonemia following different conditions paired with a dietary MCT beverage over an 8-hour metabolic day protocol.

    Secondary Outcome Measures

    1. Concentration of plasma glucose [8 hours]

      To compare acute glucose following different conditions paired with a dietary MCT beverage over an 8-hour metabolic day protocol.

    2. Concentration of plasma insulin [8 hours]

      To compare acute insulin following different conditions paired with a dietary MCT beverage over an 8-hour metabolic day protocol.

    3. Concentration of plasma free fatty acids [8 hours]

      To compare acute free fatty acids following different conditions paired with a dietary MCT beverage over an 8-hour metabolic day protocol.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • 10 health young (20-40 y old) and 10 health older (> 60 y old) participants

    • Men and women

    Exclusion Criteria:
    • smoking

    • diabetes (fasting glucose >7.0 mmol/l and glycated hemoglobin >6.9%)

    • strenuous aerobic exercise more than three times a week

    • untreated hypertension, dyslipidemia, and abnormal renal, liver, heart or thyroid function

    • under medication known to affect triglycerides and carbohydrates metabolism (i.e. diuretics, beta-blockers, steroids, insulin sensitizing)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Rearsh Centre on Aging Sherbrooke Quebec Canada J1H4C4

    Sponsors and Collaborators

    • Université de Sherbrooke

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Université de Sherbrooke
    ClinicalTrials.gov Identifier:
    NCT03830268
    Other Study ID Numbers:
    • 2017-714
    First Posted:
    Feb 5, 2019
    Last Update Posted:
    Mar 25, 2020
    Last Verified:
    Mar 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Université de Sherbrooke
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 25, 2020