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Circadian RhythmNCT06549322

Timing and Resistance Exercise: Impact on Eating and Metabolism

A study testing The exercise in morning and The exercise in evening in people with Circadian Rhythm and Energy Balance, run by National Taiwan Normal University at 1 site in Taiwan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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… Read more about this study

Who is it for?
Ages 20 to 30 years, men onlyHealthy volunteers can take part
What is being tested?
The exercise in morning and The exercise in evening
Could I receive a placebo?
No, everyone receives an active treatment
How many people
12 participants
Where
1 siteTaiwan
Study dates
1 Oct 2024to 30 Dec 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 30 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Age: 20-30
  • weight stable for at least 6 months

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

Taiwan1 site
  • National Taiwan Normal University

    Taipei, 106

Other trials in Taiwan

About this study

Official title: The Efficacy of Exercise Timing - Effects of Resistance Exercise on Eating Behavior and Energy Metabolism

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.

Being tested
The exercise in morning, The exercise in evening
Keywords
resistance exercise, energy expenditure
Medical subject headings
Appetitive Behavior

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • The exercise in morningOther

    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

  • The exercise in eveningOther

    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

Study groups in NCT06549322
Study groupRoleWhat they receive
The exercise in morningExperimentalResistance 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.
Receives: Other: The exercise in morning
The exercise in eveningExperimentalResistance 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.
Receives: Other: The exercise in evening
The control in all dayNo interventionSit and rest in the morning and evening during the day.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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.".

    Measured: 3 hours during each study intervention

  2. Change in acyl-Ghrelin

    acyl-Ghrelin in pg/mL

    Measured: 3 hours during each study intervention

  3. Change in PYY

    PYY in pg/mL

    Measured: 3 hours during each study intervention

  4. Change in Leptin

    Leptin in pg/mL

    Measured: 3 hours during each study intervention

  5. Change in lactate

    lactate in mmol/L

    Measured: 3 hours during each study intervention

  6. 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.

    Measured: 3 hours during each study intervention

  7. 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 .

    Measured: The Before day, the durning day, and the day following the experiment.

  8. Energy expenditure

    Participants will record energy expenditure during resistance exercise, with non-exercise energy expenditure measured using an accelerometer.

    Measured: The Before day, the durning day, and the day following the experiment.

Secondary outcomes (9)
  1. Explicit liking

    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."

    Measured: 3 hours during each study intervention

  2. Explicit wanting

    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."

    Measured: 3 hours during each study intervention

  3. Implicit wanting

    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.

    Measured: 3 hours during each study intervention

  4. Relative preference

    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.

    Measured: 3 hours during each study intervention

  5. Taste appeal bias

    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.

    Measured: 3 hours during each study intervention

  6. Fat appeal bias

    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.

    Measured: 3 hours during each study intervention

  7. change in Cortisol

    Cortisol mcg/dL

    Measured: 3 hours during each study intervention

  8. change in complete blood count

    change in complete blood count cells/L

    Measured: 3 hours during each study intervention

  9. change in growth hormone

    growth hormone pmol/L

    Measured: 3 hours during each study intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Aug 2024
  2. Study start1 Oct 2024
  3. Primary completion30 Dec 2025
  4. Study completion30 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Crossover
Masking
None (open label)
Enrolment
12 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06549322
Sponsor's protocol ID
202401HM008
Status last verified
Dec 2025
First submitted
8 Aug 2024
Last updated
16 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing The exercise in morning and The exercise in evening in people with Circadian Rhythm and Energy Balance, run by National Taiwan Normal University at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 16 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Subjective appetite Subjective appetite Subjective appetite Subjective appetite Subjective appetite Subjective appetite (time frame: 3 hours during each study intervention). The study lists 8 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Oct 2026.

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