Actively Recruiting

Age: 6Years - 20Years
All Genders
Healthy Volunteers
NCT05770817

The SKyRoCKeT Study

Led by University of North Carolina, Charlotte · Updated on 2026-04-29

360

Participants Needed

1

Research Sites

203 weeks

Total Duration

On this page

Sponsors

U

University of North Carolina, Charlotte

Lead Sponsor

E

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The SKyRoCKeT Study (Surface-Knit and Reformulate CADENCE-Kids for Translation) will recruit a sex- and age-balanced sample of 360 young people 6-20 years of age to develop an integrative, physiologically-coherent age-cadence-log(metabolic equivalent, MET) surface-based model, reformulate the prior R21 CADENCE-Kids study (1; NCT01989104) by providing individualized, more precise, age-specific and coherent cadence-intensity thresholds, investigate additional differences by anthropometric factors, and translate cadence-intensity thresholds to over-ground walking. The SKyRoCKeT Study is an innovative critical step to provide a coherent, interpretable, objectively monitored step-based intensity metric to inform (inter)national physical activity (PA) guidelines by transforming currently vague guidelines of PA intensity into quantifiable PA recommendations that can be of widespread use, which clinicians, young people, parents, and researchers can integrate into preventive care management and action plans for personalized care. The SKyRoCKeT Study will allow for a user-friendly, interpretable metric to more accurately inform public health/behavioral interventions, assessments, analyses, school-based health and physical education curricula and programs, and public health messages for young people and their caregivers.

CONDITIONS

Official Title

The SKyRoCKeT Study

Who Can Participate

Age: 6Years - 20Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Between 6 - 20 years of age on the day of signing the informed consent/assent.
  • Able to walk without the need of assistance
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of North Carolina at Charlotte

Charlotte, North Carolina, United States, 28223

Actively Recruiting

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Research Team

C

Catrine Tudor-Locke, PhD

CONTACT

L

Laura H Gunn, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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