Actively Recruiting
Facilitating Access to Specialty Treatment
Led by Children's Hospital of Philadelphia · Updated on 2025-06-20
210
Participants Needed
1
Research Sites
155 weeks
Total Duration
On this page
Sponsors
C
Children's Hospital of Philadelphia
Lead Sponsor
N
National Institute of Neurological Disorders and Stroke (NINDS)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this hybrid implementation-effectiveness study is to evaluate the effectiveness (hastened recovery times) and feasibility (fidelity in connecting to concussion specialty care) of a novel mobile health intervention, designed to reduce disparities in access to specialty care through the use of remote patient monitoring (RPM) to facilitate care hand-off from the emergency department (ED) to concussion specialty care. Participants will report their symptoms and activity once daily through RPM chat technology that is linked to their electronic health record and prompts referral to specialty care.
CONDITIONS
Official Title
Facilitating Access to Specialty Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Males and females age 13 - 18
- Present to the Children's Hospital of Philadelphia Emergency Department within 72 hours of head injury
- Meet concussion criteria as defined by the most recent International Consensus Statement on Concussion
- Own a smartphone
- Have moderate-to-high risk for Persistent Post-Concussion Symptoms (5P rule score >3/12)
- Child meets the study eligibility criteria (for parents)
- ED or specialty provider caring for at least one patient via the mobile health-facilitated care handoff strategy (for providers)
You will not qualify if you...
- Glasgow Coma Scale score less than 13
- Lower extremity trauma
- Prior concussion within 1 month
- Non-English speaking (for participants, parents, and providers)
- Admission to the hospital at the initial head injury visit
- Previously enrolled in the study
- Inability to complete study procedures
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States, 19104
Actively Recruiting
Research Team
M
Melissa Godfrey
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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