60 Participants NeededMy employer runs this trial

Exercise Snacking for Sedentary Lifestyle

GR
RL
Overseen ByRicky Lopez, MS
Age: 18 - 65
Sex: Any
Trial Phase: Academic
Sponsor: University of Wisconsin, River Falls
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

Regular physical activity is associated with numerous health benefits, yet many young adults do not achieve recommended levels of physical activity. Exercise snacking, which involves performing brief bouts of physical activity throughout the day, may provide a practical alternative to traditional exercise programs by making physical activity easier to incorporate into daily routines.

This randomized controlled trial will evaluate whether a 12-week exercise snacking intervention improves physical activity levels, aerobic fitness, cardiometabolic health, and psychological well-being in insufficiently active young adults. Participants will be randomly assigned to either an exercise snacking intervention or a usual behavior control group. Assessments will be completed at baseline, after the 12-week intervention, and after an additional 12-week follow-up period to determine whether any changes are maintained after the intervention ends.

The study will measure physical activity using wearable activity monitors and assess aerobic fitness, body composition, blood pressure, blood lipids, glucose, exercise motivation, affective responses to exercise, and mental well-being. The findings will help determine whether exercise snacking is an effective and sustainable strategy for improving health in young adults and may inform future physical activity recommendations and interventions

Who Is on the Research Team?

GR

Gregory Ruegsegger, PhD

Principal Investigator

University of Wisconsin, River Falls

Are You a Good Fit for This Trial?

Inclusion Criteria

I am cleared to safely do moderate-to-vigorous exercise.
Willing and able to provide written informed consent
Willing to complete all study visits, wear activity monitors, and comply with study procedures
See 3 more

Exclusion Criteria

Resting heart rate >100 beats/minute at screening
Resting blood pressure >160/100 mmHg at screening
Clinically significant electrocardiogram (ECG) abnormalities identified during screening that require medical evaluation
See 5 more

What Are the Treatments Tested in This Trial?

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Exercise SnackingExperimental Treatment1 Intervention
Group II: Usual Behavior ControlActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Wisconsin, River Falls

Lead Sponsor