The SKyRoCKeT Study: Understanding Walking Intensity in Young People

The SKyRoCKeT Study is looking for 360 healthy young people aged 6 to 20 years old who can walk without assistance. This observational study aims to better understand how walking intensity (measured by 'cadence' or steps per minute) relates to age and energy use (measured by 'MET' or metabolic equivalent). There are no interventions or medications being tested; instead, researchers will collect information about your walking patterns. The main goal is to create a more accurate way to measure walking intensity for different ages, which could help in understanding physical activity levels. We are not currently aware of the study's recruitment status.

Study design
This is an observational study with a planned enrollment of 360 participants. It is not a randomized or blinded study.
What's involved
You would participate in three visits over a period of up to three months, plus an at-home free-living protocol. During these visits, your cadence (steps per minute) will be measured.
Compensation
Not stated in the trial record.
Follow-up
Your cadence will be measured over the course of the study period, which is up to three months.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT05770817

The SKyRoCKeT Study

Recruiting
Not specifiedAges 6–20Observational
University of North Carolina, Charlotte
~360 participants
Updated 2026-04-29 on ClinicalTrials.gov
What's tested:N/A: SKyRoCKeT is an observational study

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Cadence (steps per minute)
Measured over Over the course of the study period (up to 3 months) across 3 visits plus an at-home free-living protocol per participant (see Protocol/Procedures)
Healthy
1 sites across 1 states
North Carolina1
  • Catrine Tudor-Locke, PhD · PRINCIPAL_INVESTIGATOR · University of North Carolina at Charlotte
  • Laura H Gunn, PhD · PRINCIPAL_INVESTIGATOR · University of North Carolina at Charlotte

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Between 6 - 20 years of age on the day of signing the informed consent/assent.
Able to walk without the need of assistance

Exclusion

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
  • Cadence (steps per minute)Over the course of the study period (up to 3 months) across 3 visits plus an at-home free-living protocol per participant (see Protocol/Procedures)

    Cadence (steps per minute) represents an overlooked opportunity to describe the intensity of ambulatory activity.