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Recruiting NCT06810557

NCT06810557 Brief Behavioral Sleep Intervention for Obesity Prevention in Primary Care

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Clinical Trial Summary
NCT ID NCT06810557
Status Recruiting
Phase
Sponsor Temple University
Condition Obesity, Childhood
Study Type INTERVENTIONAL
Enrollment 50 participants
Start Date 2025-05-15
Primary Completion 2026-11-30

Eligibility & Interventions

Sex All sexes
Min Age 6 Years
Max Age 11 Years
Study Type INTERVENTIONAL
Interventions
Optimize Sleep Primary Care (OSPC)Enhanced Usual Care

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 50 participants in total. It began in 2025-05-15 with a primary completion date of 2026-11-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this study is to compare two different approaches to help families with children 6-11 years enhance nighttime sleep: 1) working one-on-one with a nurse to learn effective behavioral strategies to try to improve children's sleep or 2) receiving education on a good night's sleep and its benefits. Participating families will meet with a nurse 6 times or receive 6 educational handouts. Participating families will also complete three assessments (start of the study, 2 months and 6 months) during which study questionnaires will be completed, participating children will wear devices that assess sleep and physical activity, participating families will report on what the child ate on two separate days and will be measured for height and weight.

Eligibility Criteria

Inclusion Criteria: * Patient at Temple Pediatrics * Child age 6-11 years * Child time in bed of less than 9 hours per night on most days per week * Body Mass Index (BMI) for age and biological sex great than the 10th percentile but less than the 95th percentile * Understanding of and ability to complete the protocol * Parent age at least 18 years and primary caregiver * Willingness to be randomized to either condition Exclusion Criteria: * Diagnosed sleep disorder * Medication use or diagnosis of medical or psychiatric condition that may impact sleep or weight status * Current or planned treatment for weight control

Contact & Investigator

Central Contact

Ashley Ogoe, MPH, CCRP

✉ ashley.greer@temple.edu

📞 215-707-5782

Principal Investigator

Chantelle N Hart, PhD

PRINCIPAL INVESTIGATOR

Temple University

Frequently Asked Questions

Who can join the NCT06810557 clinical trial?

This trial is open to participants of all sexes, aged 6 Years or older, up to 11 Years, studying Obesity, Childhood. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06810557 currently recruiting?

Yes, NCT06810557 is actively recruiting participants. Contact the research team at ashley.greer@temple.edu for enrollment information.

Where is the NCT06810557 trial being conducted?

This trial is being conducted at Philadelphia, United States.

Who is sponsoring the NCT06810557 clinical trial?

NCT06810557 is sponsored by Temple University. The principal investigator is Chantelle N Hart, PhD at Temple University. The trial plans to enroll 50 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology