Timing and Resistance Exercise: Impact on Eating and Metabolism
The Efficacy of Exercise Timing - Effects of Resistance Exercise on Eating Behavior and Energy Metabolism
1 other identifier
interventional
18
1 country
1
Brief Summary
Exercise timing (morning or evening) for optimal weight control is a research topic urgently addressed by scholars in the relevant field. Due to the better control of energy metabolism and physical activity levels in the morning, existing research on resistance exercise and eating behavior primarily focuses on experiments conducted in the morning, with only one study in the afternoon. No research has yet compared the potential differences between morning and evening resistance exercise. A one-year study aims to investigate the impact of morning and evening resistance exercise on physiological metabolism and eating behavior. Eighteen healthy male participants will be randomly assigned to a crossover design study, including AM exercise, PM exercise, and control (rest condition) trials. Variables including subjective appetite, appetite hormones (ghrelin, peptide YY), food preferences, ad libitum eating, dietary records, energy expenditure, and PBMCs circadian rhythm genes will be measured. This preliminary study through a multidimensional observation, the results will contribute to understanding the potential differences and mechanisms of morning and evening resistance exercise on physiological metabolism and eating behavior. In practical applications, conducting resistance exercise in the evening or at night aligns better with current lifestyles. The findings of this study can support the optimization of exercise benefits by validating the choice of exercise timing.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Sep 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 8, 2024
CompletedFirst Posted
Study publicly available on registry
August 12, 2024
CompletedStudy Start
First participant enrolled
September 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 30, 2025
CompletedAugust 12, 2024
August 1, 2024
1.3 years
August 8, 2024
August 8, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (8)
Subjective appetite Subjective appetite Subjective appetite Subjective appetite Subjective appetite Subjective appetite
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
acyl-Ghrelin in pg/mL
3 hours during each study intervention
Change in PYY
PYY in pg/mL
3 hours during each study intervention
Change in Leptin
Leptin in pg/mL
3 hours during each study intervention
Change in lactate
lactate in mmol/L
3 hours during each study intervention
Change in PBMCs circadian rhythm genes
Circadian rhythm genes in PBMC will be measured, such as Bmal1, Clock, Per1, Per2, Per3, Cry1, Cry2, Cry3, and Tbp in arbitrary units.
3 hours during each study intervention
Energy intake
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
Participants will record energy expenditure during resistance exercise, with non-exercise energy expenditure measured using an accelerometer.
The Before day, the durning day, and the day following the experiment.
Secondary Outcomes (9)
Explicit liking
3 hours during each study intervention
Explicit wanting
3 hours during each study intervention
Implicit wanting
3 hours during each study intervention
Relative preference
3 hours during each study intervention
Taste appeal bias
3 hours during each study intervention
- +4 more secondary outcomes
Study Arms (3)
The exercise in morning
EXPERIMENTALResistance 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.
The exercise in evening
EXPERIMENTALResistance 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.
The control in all day
NO INTERVENTIONSit and rest in the morning and evening during the day.
Interventions
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
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
Eligibility Criteria
You may qualify if:
- Age: 20-30
- weight stable for at least 6 months
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Taiwan Normal University
Taipei, 106, Taiwan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Hung-wen Liu, Ph.D.
National Taiwan Normal University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 8, 2024
First Posted
August 12, 2024
Study Start
September 1, 2024
Primary Completion
December 30, 2025
Study Completion
December 30, 2025
Last Updated
August 12, 2024
Record last verified: 2024-08