NCT05703347 · Children's Hospital of Philadelphia
Optimizing a Mobile Health Platform for Sleep Promotion and Obesity Prevention in Children
What this study is about
The overall objective of this application is to develop a mobile health platform for the pediatric care setting to promote longer sleep duration for childhood obesity prevention.
View original scientific description
The overall objective of this application is to develop a mobile health platform for the pediatric care setting to promote longer sleep duration for childhood obesity prevention.
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
- Aged 8-12 years olds.
- Insufficient sleep duration (\<8.5 hours per night).
- Body mass index (BMI) between the 50th and 95th percentile for age and sex.
- One child per family.
Exclusion criteria
- Diagnosed with a chronic disease.
- Diagnosed with a behavioral health problem.
- Diagnosed with a condition that can impact sleep or growth.
- Diagnosed with a condition affecting physical growth and maturation or dietary intake.
- Children with a history of cancer, kidney, GI, musculoskeletal, or sleep disorders.
- Children who will transition to high-school during the study.
- Children using steroids/hormones.
- Children regularly taking medications related to exclusionary medical conditions or that impact sleep.
- Children with a history of significant behavioral health concerns.
- Parent reported PROMIS Parent Proxy Sleep Disturbance - Short Form 8a raw score of ≥28.
Where
- Philadelphia, Pennsylvania
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 May 27, 2026 · Source of record for eligibility and locations