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Clinical Trials in Taiwan / NCT06966414
Recruiting Not applicable

Effects of Different Timing of Bodyweight High-intensity Exercise on Human Behaviours

NCT06966414 · tracked via the Priya Life Science Taiwan tracker
Phase
Not applicable
Started
2025-04-30
Last updated
2025-05-11

Condition(s) studied

Physical ActivityEnergy IntakeSedentary Behavior

Investigational drug(s) / intervention(s)

Morning exerciseEvening exercise

Morning exercise: Participants performed bodyweight exercise in the morning between 08:00 to 11:00 AM.

Evening exercise: Participants performed bodyweight exercise in the morning between 18:00 to 21:00 PM.

Study summary

The purpose of this project is to investigate the effects of exercise at different times of day on 72-hour eating behaviour, physical activity and sedentary behaviour in physically inactive adults.

Eligibility

Sex
ALL
Min age
20 Years
Max age
50 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Aged between 20 and 50 years, with a BMI ranging from 19 to 27 kg/m². * Classified as having "low" physical activity levels (750 Metabolic Equivalents / week) according to the International Physical Activity Questionnaire (IPAQ). * Engaged in moderate-intensity exercise for no more than 3 days per week and less than 30 minutes per session in the 3 months preceding the study. * Maintained a stable body weight (± 3 kg) during the 3 months prior to the main experiment. * Not taking any medications, supplements, or vitamins that might affect food intake, appetite, physical activity, weight loss, or metabolism. * Free from cardiovascular and metabolic diseases. * Not pregnant or planning to become pregnant. * Not currently on a diet or undergoing any specific dietary interventions (e.g., intermittent fasting, ketogenic diet). * No injuries or surgical wounds preventing physical activity. * Regular sleep patterns, averaging 7-9 hours per night, with no shift work. * No habits of heavy alcohol consumption or smoking. Exclusion Criteria: * Personal history of/existing diabetes, cardiovascular disease, metabolic disease or dyslipidaemia. * Taking medications that may influence lipid or carbohydrate metabolism or immune system function. * Unable to take part in exercise for any reason (e.g., injury or disability) or a positive response to any questions on the Physical Activity Readiness questionnaire (PAR-Q).

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
National Taiwan Normal University Taipei Taiwan Recruiting

More National Taiwan Normal University trials in Taiwan

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06966414 on ClinicalTrials.gov ↗ ← All trials in Taiwan