Actively Recruiting

Phase Not Applicable
Age: 13Years - 18Years
All Genders
NCT06624358

Physical Activity in CKD

Led by Children's Hospital of Philadelphia · Updated on 2025-10-02

100

Participants Needed

1

Research Sites

165 weeks

Total Duration

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Sponsors

C

Children's Hospital of Philadelphia

Lead Sponsor

N

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this is to test the efficacy of a 12-week physical activity intervention in 64 adolescents with CKD.

CONDITIONS

Official Title

Physical Activity in CKD

Who Can Participate

Age: 13Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Males or females age 13 - 18 years
  • Diagnosis of CKD stage II - V not yet on dialysis or with a transplant
  • English proficiency
  • Parental/guardian permission (informed consent), and if applicable, child assent
  • Parent/legal guardian of an enrolled adolescent participant (for caregiver participants)
  • English proficiency (for caregiver participants)
Not Eligible

You will not qualify if you...

  • Pregnant or lactating (adolescent participants)
  • Non-ambulatory (adolescent participants)
  • High physical activity at baseline (>45 min/day of moderate to vigorous physical activity)
  • Provide less than 2 days of physical activity data during the run-in period
  • Have a condition such as heart or lung disease that precludes safely engaging in physical activity
  • Have received a solid organ transplant
  • Limited English proficiency (both adolescent and caregiver participants)
  • Are on dialysis
  • Unable to comply with study protocol or deemed unsuitable by investigator for any reason

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

Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

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Research Team

J

Jillian LoGuidice, BS

CONTACT

A

Amy Kogon, MD MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

FACTORIAL

Primary Purpose

TREATMENT

Number of Arms

16

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