NCT06828835 The REPOSE (Reach for Equity in Pediatric Sleep Evaluation) Navigation Intervention
| NCT ID | NCT06828835 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Medical University of South Carolina |
| Condition | Sleep Apnea, Obstructive |
| Study Type | INTERVENTIONAL |
| Enrollment | 80 participants |
| Start Date | 2026-02-03 |
| Primary Completion | 2028-08-31 |
Eligibility & Interventions
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 80 participants in total. It began in 2026-02-03 with a primary completion date of 2028-08-31.
⚠ 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
This research study aims to find out the effect of REPOSE, a patient navigation intervention, on the receipt of equitable care among children with a broad range of socioeconomic and rural/urban status with Sleep Disordered Breathing (SDB). In the REPOSE intervention, a centralized patient navigator a) identifies and addresses dynamic individual barriers, b) provides resources and social support for parent-child dyads, and c) facilitates bidirectional SDB care coordination between clinical teams and parents to achieve evidence-based care. This study will evaluate the effects of the REPOSE intervention on SDB care delivery and clinical process outcomes for children with a broad range of socioeconomic and rural/urban status by reducing barriers and increasing self-efficacy among parents.
Eligibility Criteria
Inclusion Criteria: * Parents or caregivers (18 and older) of children who were referred by any primary care for SDB evaluation with sleep medicine or pediatric otolaryngology * Patients 2.00 to 11.99 years old * Parents with a working phone who are willing to participate in the study for a 12-month period after enrollment Exclusion Criteria: * Patients already established with sleep medicine or otolaryngology which would bias ease of completing specialty evaluation
Contact & Investigator
Phayvanh Pecha, MD
PRINCIPAL INVESTIGATOR
Medical University of South Carolina
Frequently Asked Questions
Who can join the NCT06828835 clinical trial?
This trial is open to participants of all sexes, aged 2 Years or older, up to 12 Years, studying Sleep Apnea, Obstructive. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06828835 currently recruiting?
Yes, NCT06828835 is actively recruiting participants. Contact the research team at pechap@musc.edu for enrollment information.
Where is the NCT06828835 trial being conducted?
This trial is being conducted at Charleston, United States.
Who is sponsoring the NCT06828835 clinical trial?
NCT06828835 is sponsored by Medical University of South Carolina. The principal investigator is Phayvanh Pecha, MD at Medical University of South Carolina. The trial plans to enroll 80 participants.