REPOSE Navigation for Obstructive Sleep Apnea
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores how a program called REPOSE can assist families in navigating the healthcare system to improve care for children with Sleep Disordered Breathing (SDB). The goal is to determine if a patient navigator can reduce obstacles and enhance the healthcare experience, particularly for families from diverse socioeconomic and rural or urban backgrounds. The trial compares usual care with the REPOSE intervention, which provides additional support and resources to families. This may suit parents or caregivers of children aged 2 to 11 who have been referred for SDB evaluation and have not yet consulted a specialist. Participants must have a working phone and be willing to engage in the study for a year. As an unphased trial, this study offers a unique opportunity to contribute to research that could improve healthcare navigation for families.
Do I need to stop my current medications for this trial?
The trial information does not specify whether you need to stop taking your current medications. It is best to discuss this with the trial coordinators or your doctor.
What prior data suggests that the REPOSE intervention is safe for children with sleep disordered breathing?
Research shows that the REPOSE program aids children with sleep-disordered breathing (SDB) by guiding families through the healthcare process. A patient navigator collaborates with families to identify and overcome obstacles that might delay diagnosis and treatment.
The REPOSE program focuses on support and care coordination rather than medical procedures or drugs, so it lacks typical "safety" concerns associated with medications or surgeries. The program aims to improve access to care and ensure children receive necessary treatments, emphasizing effectiveness over safety issues. Since it is not a drug or surgery, the program itself has no specific side effects.
As a non-invasive program, REPOSE is generally considered safe. Participation should not pose health risks to children, making it a promising way to improve fair access to care for those with sleep-related issues.12345Why are researchers excited about this trial?
Researchers are excited about the REPOSE intervention for obstructive sleep apnea because it tackles the issue from a fresh angle. Unlike standard treatments like CPAP machines or surgery, which focus directly on managing symptoms, REPOSE is a patient navigation strategy designed to overcome obstacles to getting a timely diagnosis and treatment. By addressing these barriers, REPOSE aims to streamline the process and ensure more patients receive the care they need more quickly. This approach could improve overall treatment accessibility and effectiveness, which is why it's generating interest.
What evidence suggests that the REPOSE intervention is effective for improving care in children with sleep disordered breathing?
Research has shown that overcoming barriers to healthcare can greatly improve health for children with obstructive sleep apnea (OSA). This trial tests the REPOSE program, a theory-based patient navigation intervention designed to address multilevel barriers to the timely diagnosis and treatment of obstructive sleep-disordered breathing. By removing obstacles and offering social support, REPOSE ensures children receive proven treatments. Strong evidence indicates that timely and well-organized care can better manage symptoms. This support may help more children benefit from treatments that lessen the severity of OSA.12467
Who Is on the Research Team?
Phayvanh Pecha, MD
Principal Investigator
Medical University of South Carolina
Are You a Good Fit for This Trial?
This trial is for parents or caregivers of children aged 2 to almost 12 years who were referred for Sleep Disordered Breathing (SDB) evaluation. Participants must have a working phone and commit to the study for 12 months.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Intervention
The REPOSE intervention is implemented, where a centralized patient navigator identifies and addresses barriers, provides resources, and facilitates care coordination for SDB
Follow-up
Participants are monitored for adherence to evidence-based guidelines and changes in barrier resolution and self-efficacy
Evaluation
Evaluation of the intervention's impact on SDB care delivery and clinical process outcomes
What Are the Treatments Tested in This Trial?
Interventions
- REPOSE
Trial Overview
The REPOSE intervention is being tested, which involves a patient navigator helping overcome barriers, providing support, and coordinating care between clinical teams and parents to ensure evidence-based treatment for SDB in children.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
The ordinary course of care.
REPOSE is a theory-based patient navigation intervention to address multilevel barriers to timely diagnosis and treatment of obstructive sleep-disordered breathing.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Medical University of South Carolina
Lead Sponsor
National Heart, Lung, and Blood Institute (NHLBI)
Collaborator
Citations
The REPOSE (Reach for Equity in Pediatric Sleep ...
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 ...
Comparative outcomes in obstructive sleep apnea therapy
The results support the hypothesis that surgery for OSA can be at least as effective as CPAP. Yet, this is another study that suggests it is ...
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employer.myhealthtoolkitbsa.com
employer.myhealthtoolkitbsa.com/web/public/brands/medicalpolicy/external-policies/surgical-treatment-of-snoring-and-obstructive-sleep-apnea-syndrome/Surgical Treatment of Snoring and Obstructive Sleep Apnea ...
The trial indicates reductions in snoring, but limited efficacy on the Apnea/Hypopnea Index (AHI) or symptoms in patients with mild-to-moderate OSA. The ...
Pharyngeal suspension suture with Repose bone screw ...
Two-month outcomes were less (activity level, energy/fatigue, and sleepiness). Fewer changes were observed in snorers than in OSA patients. There were 6 ...
Obstructive Sleep Apnea in Children
Results showed a statistically significant 46% reduction in AHI (p = 0.00001), with 80% of patients demonstrating improvement and 28% achieving complete ...
Referral of adults with obstructive sleep apnea for surgical ...
The primary outcome was the apnea-hypopnea index (AHI), as many study investigators defined surgical success as a 50% reduction in AHI to a level less than 20 ...
Obstructive Sleep Apnea in Adults - Medical Clinical Policy ...
The results of 3 to 6 months of follow-up showed surgical response rates were 80 % in severe apneics and 100 % in mild apneics. However, Verse et al also noted ...
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