NCT06888011 · University of Kansas Medical Center
iAmHealthy Clinical Practice Guideline (CPG)
What this study is about
The current study is a multilevel factorial design RCT with interventions at the clinic (Healthy Clinic intervention period vs. Control period) and individual patient levels (iAmHealthy vs. Newsletter).
View original scientific description
The current study is a multilevel factorial design RCT with interventions at the clinic (Healthy Clinic intervention period vs. Control period) and individual patient levels (iAmHealthy vs. Newsletter).
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- for individual participants:
- Child is ages 6-11 years at consent
- Child BMI %ile is ≥85th
- Child lives in a rural area
- Child/family speaks English or Spanish
Exclusion criteria
- for individual participants:
- Child has a physical limitation or injury that substantially limits physical mobility or has a planned medical treatment during the course of the trial that will substantially limit physical mobility
- Child has a known medical issue that could affect protocol compliance (e.g., cancer)
- Child and/or primary caregiver has a developmental delay or cognitive impairment that could affect protocol compliance
- Child is enrolled in a weight-loss trial
- Child has a sibling who has already consented in the trial Inclusion criteria for clinics:
- History of collaboration with site awardee in research or quality improvement projects
- In the past year at least 300 eligible potential participants
- The clinic must have an electronic medical records system Exclusion criteria for clinics:
- Unable to generate lists of children seen in clinic by date of visit, age, and zip code
Where
- Kansas City, Kansas
- Omaha, Nebraska
- Oklahoma City, Oklahoma
- Charleston, South Carolina
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Apr 13, 2026 · Source of record for eligibility and locations