- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06549322
Timing and Resistance Exercise: Impact on Eating and Metabolism
The Efficacy of Exercise Timing - Effects of Resistance Exercise on Eating Behavior and Energy Metabolism
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Hung-Wen Liu, Ph.D.
- Phone Number: +886 0277496863
- Email: hwliu@ntnu.edu.tw
Study Locations
-
-
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Taipei, Taiwan, 106
- National Taiwan Normal University
-
Contact:
- Hung Wen Liu, Ph.D.
- Phone Number: +886 0277496863
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age: 20-30
- weight stable for at least 6 months
Exclusion Criteria:
- Obesity (BMI > 30 kg/m² or body fat percentage > 25%)
- Hypertension (blood pressure over 140/90 mmHg)
- Heart disease
- Cancer
- Liver or kidney diseases
- Any other conditions that could potentially influence the study's outcomes
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: The exercise in morning
Resistance exercises are in the following order: squat, bench press, deadlift.
Each exercise consists of 3 sets with 7 repetitions, using a load of 70% 1RM with 60 sec of rest between sets.
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Resistance exercises are in the following order: squat, bench press, deadlift. Each exercise consists of 3 sets with 7 repetitions, using a load of 70% 1RM with 60 sec of rest between sets. Exercise timing: AM 11:00-11:30 |
|
Experimental: The exercise in evening
Resistance exercises are in the following order: squat, bench press, deadlift.
Each exercise consists of 3 sets with 7 repetitions, using a load of 70% 1RM with 60 sec of rest between sets.
|
Resistance exercises are in the following order: squat, bench press, deadlift. Each exercise consists of 3 sets with 7 repetitions, using a load of 70% 1RM with 60 sec of rest between sets. Exercise timing: PM 05:00-05:30 |
|
No Intervention: The control in all day
Sit and rest in the morning and evening during the day.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Subjective appetite Subjective appetite Subjective appetite Subjective appetite Subjective appetite Subjective appetite
Time Frame: 3 hours during each study intervention
|
The appetite perceptions are obtained through a 0-100 mm visual analog scale.
The variables assessed include perceptions of hunger (i.e., "How hungry do you feel?"), satisfaction (i.e., "How satisfied do you feel?"), fullness (i.e., "How full do you feel?"), prospective food consumption (i.e., "How much do you think you can eat?"), and nausea (i.e., "How nauseous do you feel?"), with 0 indicating "not at all" and 100 signifying "extremely.".
|
3 hours during each study intervention
|
|
Change in acyl-Ghrelin
Time Frame: 3 hours during each study intervention
|
acyl-Ghrelin in pg/mL
|
3 hours during each study intervention
|
|
Change in PYY
Time Frame: 3 hours during each study intervention
|
PYY in pg/mL
|
3 hours during each study intervention
|
|
Change in Leptin
Time Frame: 3 hours during each study intervention
|
Leptin in pg/mL
|
3 hours during each study intervention
|
|
Change in lactate
Time Frame: 3 hours during each study intervention
|
lactate in mmol/L
|
3 hours during each study intervention
|
|
Change in PBMCs circadian rhythm genes
Time Frame: 3 hours during each study intervention
|
Circadian rhythm genes in PBMC will be measured, such as Bmal1, Clock, Per1, Per2, Per3, Cry1, Cry2, Cry3, and Tbp in arbitrary units.
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3 hours during each study intervention
|
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Energy intake
Time Frame: The Before day, the durning day, and the day following the experiment.
|
Participants will be required to record their diet for the day before, the current day, and the day following the experiment. The energy intake include absolute energy intake and relative energy intake . |
The Before day, the durning day, and the day following the experiment.
|
|
Energy expenditure
Time Frame: The Before day, the durning day, and the day following the experiment.
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Participants will record energy expenditure during resistance exercise, with non-exercise energy expenditure measured using an accelerometer.
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The Before day, the durning day, and the day following the experiment.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Explicit liking
Time Frame: 3 hours during each study intervention
|
A visual analog scale ranging from 0 to 100 mm is utilized to evaluate the question, "How pleasant would it be to taste some of this food now?" with 0 indicating "not at all" and 100 signifying "extremely."
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3 hours during each study intervention
|
|
Explicit wanting
Time Frame: 3 hours during each study intervention
|
A visual analog scale ranging from 0 to 100 mm is utilized to evaluate the question, "How much do you want some of this food now?" with 0 indicating "not at all" and 100 signifying "extremely."
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3 hours during each study intervention
|
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Implicit wanting
Time Frame: 3 hours during each study intervention
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Participants are given a set of food image pairs and are asked to select their preference by answering the question, "Which food do you desire the most at the moment?".
The implicit wanting calculation involves further consideration of response time data based on preference choices using a standardized equation.
|
3 hours during each study intervention
|
|
Relative preference
Time Frame: 3 hours during each study intervention
|
Participants are given a set of food image pairs and are asked to select their preference by answering the question, "Which food do you desire the most at the moment?".
The relative preference is the sum of the times each type of food is chosen, with a maximum value of 48 and a minimum value of 0.
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3 hours during each study intervention
|
|
Taste appeal bias
Time Frame: 3 hours during each study intervention
|
Taste preference (savoury or sweet) is calculated by subtracting the mean savory scores from the mean sweet scores.
Positive values suggest a preference for sweet foods, while negative scores indicate a preference for savory foods, and a score of 0 signifies an equal preference between taste categories.
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3 hours during each study intervention
|
|
Fat appeal bias
Time Frame: 3 hours during each study intervention
|
Fat preference (high or low) is calculated by subtracting the mean low-fat scores from the mean high-fat scores.
Positive values suggest a preference for high-fat foods, while negative scores indicate a preference for low-fat or savory foods, and a score of 0 signifies an equal preference between fat content.
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3 hours during each study intervention
|
|
change in Cortisol
Time Frame: 3 hours during each study intervention
|
Cortisol mcg/dL
|
3 hours during each study intervention
|
|
change in complete blood count
Time Frame: 3 hours during each study intervention
|
change in complete blood count cells/L
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3 hours during each study intervention
|
|
change in growth hormone
Time Frame: 3 hours during each study intervention
|
growth hormone pmol/L
|
3 hours during each study intervention
|
Collaborators and Investigators
Investigators
- Principal Investigator: Hung-wen Liu, Ph.D., National Taiwan Normal University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 202401HM008
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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