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Exercise Snacking Impact on Physical Activity, Cardiometabolic Health, and Psychological Well-Being in Young Adults

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Study Aim

This study aims to explore how incorporating short bursts of exercise, known as 'exercise snacking', impacts daily physical activity, cardiometabolic health, and psychological well-being in young adults, measured using an accelerometer worn for seven consecutive days.

What is being tested

Exercise Snacking

Behavioral
Who is being recruted

Behavior

+ Motor Activity

+ Sedentary Behavior

From 18 to 60 Years
+14 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Basic Science Study

Interventional
Study Start: August 2026
See protocol details

Summary

Principal SponsorUniversity of Wisconsin, River Falls
Study ContactGregory Ruegsegger, PhDMore contacts
Last updated: July 21, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: August 1, 2026

Actual date on which the first participant was enrolled.

Regular physical activity reduces the risk of cardiovascular disease, type 2 diabetes, obesity, and other chronic health conditions. Despite these well-established benefits, many young adults do not achieve recommended levels of physical activity. Commonly reported barriers include limited time, competing academic or work demands, and difficulty maintaining structured exercise programs. Exercise snacking, defined as accumulating multiple brief bouts of moderate-to-vigorous physical activity throughout the day, has emerged as a potential strategy for increasing physical activity while minimizing many of the barriers associated with traditional exercise programs. Although short bouts of physical activity have demonstrated favorable acute physiological effects, relatively few randomized controlled trials have evaluated whether exercise snacking produces sustained improvements in objectively measured physical activity, physical fitness, cardiometabolic health, and psychological outcomes in free-living young adults. The purpose of this study is to determine whether a 12-week exercise snacking intervention improves physical activity behavior, aerobic fitness, cardiometabolic health, exercise motivation, affective responses to physical activity, and psychological well-being compared with a usual behavior control group. Participants will be randomly assigned to either an exercise snacking intervention or a control condition. Following completion of the intervention, participants will be observed for an additional 12 weeks to evaluate the maintenance of behavioral and physiological changes after structured support is withdrawn. The primary objectives are to determine whether exercise snacking increases objectively measured physical activity and improves aerobic fitness. Secondary objectives are to evaluate changes in body composition, blood pressure, fasting cardiometabolic biomarkers, exercise motivation, affective responses to exercise, and psychological well-being. Exploratory analyses will examine whether changes in motivation and affective responses are associated with long-term maintenance of physical activity during the follow-up period. This study will contribute to the growing evidence regarding practical, scalable approaches for increasing physical activity among young adults and may help inform future lifestyle interventions and public health recommendations aimed at promoting long-term engagement in regular physical activity

Principal SponsorUniversity of Wisconsin, River Falls
Study ContactGregory Ruegsegger, PhDMore contacts
Last updated: July 21, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

60 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Basic Science Study

Basic science studies help researchers understand how the body works or how a disease develops. They don't test treatments, but they build the foundation for future therapies.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 60 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

BehaviorMotor ActivitySedentary Behavior

Criteria

6 inclusion criteria required to participate
Able to safely participate in moderate-to-vigorous physical activity as determined by study screening procedures, including completion of the Physical - Activity Readiness Questionnaire (PAR-Q+) and health history review

Willing and able to provide written informed consent

Age 18-60 years

Willing to complete all study visits, wear activity monitors, and comply with study procedures

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8 exclusion criteria prevent from participating
Resting blood pressure > 160/100 mmHg at screening

Known cardiovascular, pulmonary, metabolic, neurological, orthopedic, or other medical conditions that would make participation in moderate-to-vigorous physical activity unsafe

Clinically significant electrocardiogram (ECG) abnormalities identified during screening that require medical evaluation

Current participation in regular structured physical activity that meets or exceeds recommended physical activity guidelines

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Participants assigned to the exercise snacking group will complete a 12-week intervention consisting of multiple brief bouts (approximately 1-3 minutes each) of moderate-to-vigorous physical activity performed throughout the day. Participants will receive written instructions, examples of appropriate exercise snacks, and periodic check-ins to support adherence. The intervention is designed to increase daily physical activity by integrating short bouts of exercise into normal daily routines.

Group II

No Intervention
Participants assigned to the control group will continue their usual daily activities for 12 weeks and will not receive instruction regarding exercise snacking or any structured physical activity program during the intervention period. They will complete the same outcome assessments as participants in the intervention group.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

University of Wisconsin-River Falls

River Falls, United StatesOpen University of Wisconsin-River Falls in Google Maps
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One Study Center
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