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The Effect of Different Methods for Modulating Postprandial Fat Oxidation on Postprandial Lipemia the Next Day

Primary Purpose

Time-restricted Feeding, Postprandial Lipemia

Status
Completed
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
time-restricted feeding trial
Sponsored by
National Taiwan Sport University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Time-restricted Feeding focused on measuring intermittent fasting

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • All the participants had not undergone physical training;
  • they did not exercise regularly;
  • and they did not have any diseases that would prevent them from performing exercises, such as high blood pressure, hyperlipidemia, heart disease, joint disease, and osteoporosis.

Exclusion Criteria:

  • Undergone physical training;
  • Exercise regularly;
  • Have any diseases that would prevent them from performing exercises, such as high blood pressure, hyperlipidemia, heart disease, joint disease, and osteoporosis.

Sites / Locations

  • National Taiwan University of Sport

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

time-restricted feeding trial

control trial

Arm Description

The participants were divided into the time-restricted feeding trial for 5 days

The participants in the control trial did not practice intermittent fasting methods

Outcomes

Primary Outcome Measures

postprandial triglycerides concentrations
postprandial triglycerides concentrations (mmol/L)
postprandial glucose concentrations
postprandial glucose concentrations (mmol/L)
postprandial insulin concentrations
postprandial insulin concentrations (pmol/L)
postprandial free fatty acid concentrations
postprandial FFA concentrations (mmol/L)
postprandial glycerol concentrations
postprandial glycerol concentrations (umol/L)

Secondary Outcome Measures

fat oxidation
fasting fat oxidation rate (g/min-1)

Full Information

First Posted
February 2, 2022
Last Updated
February 17, 2022
Sponsor
National Taiwan Sport University
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1. Study Identification

Unique Protocol Identification Number
NCT05251103
Brief Title
The Effect of Different Methods for Modulating Postprandial Fat Oxidation on Postprandial Lipemia the Next Day
Official Title
Time-restricted Feeding Increases Fat Oxidation Rate But Not Affect Postprandial Lipemia: a Crossover Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
June 4, 2021 (Actual)
Primary Completion Date
February 3, 2022 (Actual)
Study Completion Date
February 3, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Taiwan Sport University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Background: Studies have revealed that time-restricted feeding affects the fat oxidation rate; however, its effects on the fat oxidation rate and hyperlipidemia following high-fat meals are unclear. This study investigated the effects of 5-day time-restricted feeding on the fat oxidation rate and postprandial lipemia following high fat meals. Methods: In this random crossover experimental study, eight healthy male adults were included each in the 5-day time-restricted feeding trial and the control trial. The meals of the time-restricted feeding trial were provided at 12:00, 16:00, and 20:00. The meals of the control trial were provided at 08:00, 14:00, and 20:00. The contents of the meals of both trials were the same, and the calories of the meals met the 24-hour energy requirement of the participants. After 5 days of the intervention, the participants consumed high-fat meals on the sixth day, and their physiological changes were determined.
Detailed Description
The experiment was conducted over 6 days. On the first day, the participants arrived at the laboratory at 08:00 and quietly rested for 20 minutes in the supine position; gas analyzers were used to record their energy consumption. Subsequently, the participants were randomly allocated to the time-restricted feeding trial or the control trial. The meals of the time-restricted feeding trial were provided at 12:00, 16:00, and 20:00, and the participants were required to consume all the food during this time. The meals of the control trial were provided at 08:00, 14:00, and 20:00, but the consumption time was not limited. In addition to regular meals, a snack with approximately 200 calories was provided to the participants for consumption. The participants in the time-restricted feeding trial were only allowed to consume the snack from 12:00 to 20:00, whereas no restrictions were imposed on the control trial for snack consumption. The meals of the participants were provided by dieticians. Based on the results of the pretest, the calories of each meal met the daily energy requirement of the participants. The macronutrient consumption for TRF and CON were listed in table 1. After experiment completion on the fifth day, the participants returned to the laboratory on the eighth day from 08:00 to 09:00. They rested for 10 minutes in the supine position, and gas analyzers were used to collect the gas data of the participants for 20 minutes. Next, a catheter was inserted into the forearm of each participant to collect fasting blood samples. After blood sample collection, the participants were provided with a specific high-fat meal. The participants rested quietly in the laboratory for 4 hours, and their blood lipid changes during this period were observed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Time-restricted Feeding, Postprandial Lipemia
Keywords
intermittent fasting

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
8 (Actual)

8. Arms, Groups, and Interventions

Arm Title
time-restricted feeding trial
Arm Type
Experimental
Arm Description
The participants were divided into the time-restricted feeding trial for 5 days
Arm Title
control trial
Arm Type
Experimental
Arm Description
The participants in the control trial did not practice intermittent fasting methods
Intervention Type
Other
Intervention Name(s)
time-restricted feeding trial
Intervention Description
The 5-day time-restricted feeding trial and the control trial. The meals of the time-restricted feeding trial were provided at 12:00, 16:00, and 20:00.
Primary Outcome Measure Information:
Title
postprandial triglycerides concentrations
Description
postprandial triglycerides concentrations (mmol/L)
Time Frame
on the 6th day
Title
postprandial glucose concentrations
Description
postprandial glucose concentrations (mmol/L)
Time Frame
on the 6th day
Title
postprandial insulin concentrations
Description
postprandial insulin concentrations (pmol/L)
Time Frame
on the 6th day
Title
postprandial free fatty acid concentrations
Description
postprandial FFA concentrations (mmol/L)
Time Frame
on the 6th day
Title
postprandial glycerol concentrations
Description
postprandial glycerol concentrations (umol/L)
Time Frame
on the 6th day
Secondary Outcome Measure Information:
Title
fat oxidation
Description
fasting fat oxidation rate (g/min-1)
Time Frame
on the 6th day

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: All the participants had not undergone physical training; they did not exercise regularly; and they did not have any diseases that would prevent them from performing exercises, such as high blood pressure, hyperlipidemia, heart disease, joint disease, and osteoporosis. Exclusion Criteria: Undergone physical training; Exercise regularly; Have any diseases that would prevent them from performing exercises, such as high blood pressure, hyperlipidemia, heart disease, joint disease, and osteoporosis.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
ChihHui Chiu, PhD
Organizational Affiliation
National Taiwan University of Sport
Official's Role
Study Chair
Facility Information:
Facility Name
National Taiwan University of Sport
City
Taichung
ZIP/Postal Code
404
Country
Taiwan

12. IPD Sharing Statement

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The Effect of Different Methods for Modulating Postprandial Fat Oxidation on Postprandial Lipemia the Next Day

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