Effects of Exercise Snacks and Sprint Interval Training in Overweight Adults
NCT ID: NCT06849453
Last Updated: 2025-02-27
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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
NA
45 participants
INTERVENTIONAL
2025-02-24
2025-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Sprint Snacks: The Effects of Prolonged Rest on Reduced Exertion Interval Training.
NCT03159949
Effect of Low Volume Sprint Interval Training on Cardiorespiratory Fitness
NCT07328568
Efficacy of Sprint Interval Training on Anthropometric Measures
NCT04323995
Effects of SIT Combined with Remote Ischemic Preconditioning on Vascular Function in Young Women with Masked Obesity
NCT06664281
Sprint to Fitness: Effect of Outcome Expectations on Responses to Interval Exercise Training
NCT03162978
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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):
1. A control group that will not receive any treatment.
2. Two experimental groups (ES and SIT), which will undergo a stair climbing-based physical training program following the initial evaluation. The two exercise interventions are designed with equal exercise volume, with the only difference being the rest (recovery) time between stair sprints. All exercise sessions are conducted under the supervision of professionals.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Exercise snacks group
Exercise snacks group
Exercise snacks on the stairs for 8 weeks.
Sprint interval training group
Sprint interval training group
Sprint interval training on the stairs for 8 weeks.
Control group
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Exercise snacks group
Exercise snacks on the stairs for 8 weeks.
Sprint interval training group
Sprint interval training on the stairs for 8 weeks.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Overweight but not obese (BMI ≥24 and ≤ 28 kg/m2);
* Physically inactive (3 or less bouts of purposeful exercise per week);
* Ability to understand the research details and voluntarily sign the informed consent form;
* Non-smoker (for \>5 years);
* Body weight has been stable over the past six months, with no recent weight gain or loss behaviors;
Exclusion Criteria
* Individuals with a history of bone, joint or neuromuscular problems or a current musculoskeletal injury ascertained through preliminary screening;
* Abnormal electrocardiogram (ECG) results;
* Currently taking medication that may affect physiological testing;
* Contraindications to exercise.
18 Years
35 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Beijing Sport University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
School of Sports Medicine and Rehabilitation, Beijing Sport University
Beijing, , China
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
EESSITOA
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.