Developing a model for measuring physical activity in young people
Official title: Surface-Knit and Reformulate CADENCE-Kids for Translation: The SKyRoCKeT Study
Run by University of North Carolina, Charlotte · NCT05770817 · Data updated 2026-11-12
This study is trying to create a better way to measure how active young people are so that parents and doctors can help them live healthier lives.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 6 Years to 20 Years |
| Sex | All |
| Enrollment | 360 (estimated) |
| Sponsor | University of North Carolina, Charlotte Academic / other |
| Locations | 1 site (Charlotte, North Carolina) |
| Status | Recruiting |
| Started | April 5, 2023 |
| Main results expected | March 2027 |
| Study ends | March 2027 |
| Registry record updated | April 29, 2026 |
| Trial ID | NCT05770817 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are healthy young individuals aged 6 to 20 who can walk independently.
✕Probably not a fit
Patients who require assistance with walking or have significant medical conditions affecting their ability to exercise may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The SKyRoCKeT Study aims to recruit a balanced sample of 360 young individuals aged 6-20 to create a precise model for measuring physical activity intensity based on age and cadence. This observational study will reformulate previous findings from the CADENCE-Kids study by providing individualized cadence-intensity thresholds and utilizing advanced wearable technologies for data collection. The goal is to translate these thresholds into actionable guidelines that can be used by clinicians, parents, and researchers to promote healthier lifestyles among youth.
Why it matters
Potential benefit: If successful, this study could lead to more effective physical activity guidelines tailored for young people, enhancing their health and fitness.
How similar studies have gone: Previous studies, such as CADENCE-Kids, have laid the groundwork for this approach, indicating potential for success in similar methodologies.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Between 6 - 20 years of age on the day of signing the informed consent/assent. * Able to walk without the need of assistance Exclusion Criteria: * Need for assistance with walking including the use of a wheelchair * Mental illness requiring hospitalization within the past 5 years * Medical condition or medications that affect(s) changes in heart rate with exercise * Current pregnancy * Pacemaker or other implanted medical device including metal joint replacements * History of cardiovascular disease, stroke, transient ischemic attacks (TIA, mini-stroke), chest pain, unusual shortness of breath during physical activity/exercise, swelling in legs/ankles, or excessive leg pain with exercise. * History of musculoskeletal problems that cause pain during physical activity which interferes with the ability to walk * Exercise-induced asthma requiring medications prior to low intensity activities like walking * Unavailable for the entire duration of the study period
Where it's running
-
University of North Carolina at Charlotte
Charlotte, North Carolina, United States Recruiting
Study contacts
- Principal investigator: Catrine Tudor-Locke, PhD — University of North Carolina at Charlotte
- Study coordinator: Catrine Tudor-Locke, PhD
- Email: tudor-locke@uncc.edu
- Phone: 704-687-7917
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.