School of Sports Medicine and Rehabilitation, Beijing Sport University
Beijing, China
NCT Number: NCT06849453
Exploring the efficacy and acceptability of exercise snacks (ES) and sprint interval training (SIT) could provide time-efficient, low-barrier alternatives for individuals, especially those who, due to 'lack of time, environment, and equipment,' struggle to meet traditional physical activity recommendations. This research aims to investigate the effects of ES and SIT, of equal exercise volume, on overweight adults.
Trial opening soon.
Get Notified18 year–35 year
All sexes
Interventional
Not applicable
Beijing, China
Engaging in regular physical activity has been shown to induce a range of beneficial physiological and psychological adaptations, including improved cardiorespiratory fitness, body composition, cardiovascular function, and reductions in negative emotions. However, global participation rates in physical activity remain suboptimal, with little significant improvement. Interviews and surveys have identified several potential barriers to low physical activity levels, with limitations such as 'lack of time, equipment, and facilities' often cited as the main perceived obstacles. Therefore, exploring the minimum effective dose of exercise in real-world settings is essential.
This study will employ a randomized clinical trial to examine the effectiveness and acceptability of two low-volume, high-intensity stair climbing exercises in overweight adults. It adopts a single-blind, parallel randomized design, with the intervention commencing immediately after the initial evaluation and randomization, following a pre-treatment/post-test framework. Eligible participants were recruited via convenience sampling and randomly assigned to one of three groups (one control group and two experimental groups):
The aim of this study is twofold: First, to explore the impact of ES and SIT on cardiorespiratory fitness, body composition, and cardiovascular function in overweight adults. Second, to examine the acceptability of two low-volume, high-intensity stair climbing exercises by assessing participants' (1) acceptability, (2) reactions during the interventions, (3) enjoyment and affective valence during exercise, and (4) intentions at the end.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Exercise snacks on the stairs for 8 weeks.
Sprint interval training on the stairs for 8 weeks.
Time frame: 8 weeks
The change of maximal oxygen uptake (VO2max) before and after intervention.
Time frame: 8 weeks
The change of body composition indexes (including fat mas, lean body mass, percentage of body fat) before and after intervention.
Time frame: 8 weeks
The changes in concentrations of high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, total cholesterol, and triglyceride before and after intervention.
Time frame: 8 weeks
The change of brachial Flow-Mediated Dilation (FMD) before and after intervention. Endothelial function will be assessed by FMD.
Time frame: 8 weeks
The changes of brachial-ankle pulse wave velocity and ankle brachial index before and after intervention.
Time frame: 8 weeks
The change of blood pressure (including systolic and diastolic blood pressure) before and after intervention.
Time frame: 8 weeks
The change of resting heart rate before and after intervention.
Time frame: 8 weeks
The change of waist circumference before and after intervention.
Time frame: 8 weeks
The change of hip circumference before and after intervention.
Time frame: 8 weeks
The change of BMI before and after intervention. BMI is calculated from the formula, Weight (kg) / Height2 (m2).
Time frame: 8 weeks
Intervention acceptability will be assessed using a theoretical framework of acceptability (TFA) questionnaire, completed only at the follow-up assessment. The seven domains of the TFA, along with overall acceptability, are measured using an 8-item questionnaire. The scale scores range from 0 to 5 with high scores indicating greater acceptability, and the total score representing the mean average of 7 individual domains of acceptability (each also rated 0-5).
Time frame: 8 weeks
A modified version of the PACES will be used, the PACES scale was modified by removing 1 irrelevant item ('I was very/not at all absorbed in the activity'). The 17 items are scored on a 7-point Likert scale, resulting in an overall enjoyment score between 17 (not enjoyable), 68 (neutral), and 119 (enjoyable).
Time frame: 8 weeks
Intention questionnaire will be used after the 8 weeks intervention by a seven-point scale ranging from "Most likely never do this form of physical activity again (1)" to "Will likely do this three times per week every week (7)".
Time frame: 4 weeks and 8 weeks
Exercise enjoyment scale will be measured before, middle, and after intervention. The form will be presented to participants on a scale of 1 = 'not at all' to 7 = 'extremely,' and they will be asked, 'How much did you enjoy this exercise session?'
Time frame: 4 weeks and 8 weeks
Feeling scale will be measured before, middle, and after intervention. The one-item Feeling Scale will be used to measure general affective valence (i.e., pleasure and displeasure), participants will respond to the question 'How are you feeling right now?' (-5 = very bad to +5 = very good)
Time frame: 4 weeks and 8 weeks
Participants' RPE will be immediately assessed by Borg's Category-Ratio 10 scale after training sessions before, middle, and after intervention. The scale scores range from 0 to 10, with higher scores indicating greater perceived exertion.
Time frame: 4 weeks and 8 weeks
Mean and maximum heart rate of the intervention group will be monitored during each sprint.
Time frame: 8 weeks
DASS-21 will be used before and after intervention. The scale has 21 questions, each question required participants to rate their experiences on a 4-point scale, where 0 indicated "did not apply to me at all", 1 indicated "applied to me to some degree or some of the time", 2 indicated "applied to me to a considerable degree or a good part of the time", and 3 indicated "applied to me very much or most of the time". The total scale scores range from 0 to 63, with higher scores indicating worse outcomes.
Contact information is provided by the study sponsor or research team.
Beijing Sport University
Other
Effects of Exercise Snacks and Sprint Interval Training on Cardiovascular Function in Overweight Adults: A Randomized Controlled Trial
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07590219
Body Weight, Cardiovascular Function
São Paulo, Brazil
View Trial DetailsNCT06811324
Atrophy, Body Weight
San Antonio, Texas, United States
View Trial DetailsNCT05872139
Aging, Arterial Stiffness
Muncie, Indiana, United States
View Trial DetailsNCT03104387
Cardiovascular Function, Genotoxicity
Copenhagen, Denmark
View Trial Details