Effects of Different Timing of Brisk Walking on Human Behaviours
NCT ID: NCT06962566
Last Updated: 2025-05-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
30 participants
INTERVENTIONAL
2024-07-23
2025-03-24
Brief Summary
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Detailed Description
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During a one-week preliminary test, participants were instructed to record their physical activity levels measured in steps, sleep duration including wake-up and sleep times, and dietary behaviours through photographs taken (2 weekdays and 1 weekend day) over a period of 7 consecutive days. Participants were allowed to take part in this study, once they met the inclusion criteria: 1) an average daily step count of less than 7,500 over the course of the week and 2) a wake-up time no later than 11:00 AM).
Exercise intervention During the main trials, two main trials, separated by at least one week, were conducted - exercise in the morning (08:00 to 11:00 AM) or exercise in the evening (18:00 to 21:00 PM).
In both trials, participants completed the first Visual Analogue Scale (VAS) for subjective appetite upon waking, wore a pedometer and an accelerometer, and recorded energy intake and physical activity over a 3-day period (the day before exercise intervention, the exercise day and the day after exercise intervention). Upon arrival at the laboratory, participants completed the second VAS, followed by a 15-minute waiting period before commencing the exercise. Participants then performed a 45-minute treadmill brisk walk (6.4 km/h for males, 6.0 km/h for females), followed by a 15-minute rest period, after which they completed the third VAS.
Heart rate and Rating of Perceived Exertion (RPE) were measured every 15 minutes during exercise. Energy balance (e.g., energy intake and spontaneous physical activity) was assessed using a food diary, Actigraph wGT3x-BT accelerometer (Actigraph Co., Ltd., Pensacola, FL, USA), and pedometer (Realalt, Goldhat Ltd., UK), which were worn starting from the night two days before the experiment and removed after waking up two days post-experiment.
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
NONE
Study Groups
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Morning exercise
Brisk walking in the morning
Morning exercise
Participants performed a 45-minute treadmill brisk walking in the morning between 08:00 to 11:00 AM.
Evening exercise
Brisk walking in the evening
Evening exercise
Participants performed a 45-minute treadmill brisk walking in the evening between 18:00 to 21:00 PM.
Interventions
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Morning exercise
Participants performed a 45-minute treadmill brisk walking in the morning between 08:00 to 11:00 AM.
Evening exercise
Participants performed a 45-minute treadmill brisk walking in the evening between 18:00 to 21:00 PM.
Eligibility Criteria
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Inclusion Criteria
* 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
* 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).
20 Years
50 Years
ALL
Yes
Sponsors
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National Taiwan Normal University
OTHER
Responsible Party
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Yung-Chih Chen
Principal Investigator
Locations
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National Taiwan Normal University
Taipei, , Taiwan
Countries
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Other Identifiers
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202405HM084-1
Identifier Type: -
Identifier Source: org_study_id
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