Loading clinical trials...

RECRUITINGNA

Facilitating Access to Specialty Treatment

Utilizing Mobile Health to Expedite Access to Specialty Care for Youth Presenting to the Emergency Department With Concussion at Highest Risk of Developing Persisting Symptoms

NCT05741411•Children's Hospital of Philadelphia

View on ClinicalTrials.gov

Summary

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.

Eligibility

Age

13 - 18 years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•Males and females age 13 - 18
•Present to the Children's Hospital of Philadelphia (CHOP) Emergency Department (ED) within 72 hours of head injury
•Meet criteria for concussion as defined by the most recent International Consensus Statement on Concussion
•Own a smartphone
•Meet criteria for moderate-to-high risk for Persistent Post-Concussion Symptoms according to 5P rule (score \>3/12)
•Child meets the study eligibility criteria
•ED or specialty provider caring for at least one patient via the mobile Health (mHealth)-facilitated care handoff strategy

Exclusion Criteria

•Glasgow Coma Scale score \<13
•Lower extremity trauma
•A prior concussion within 1 month
•Non-English speaking
•Admission to the hospital at the initial head injury visit
•Previously enrolled in the study
•Inability to complete study procedures.
•Non-English speaking
•Non-English speaking

Locations (1)

Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States

Key Dates

Start Date

March 11, 2024

Primary Completion Date

September 1, 2026

Completion Date

March 1, 2027

Last Updated

June 20, 2025

Enrollment

210

ESTIMATED participants

Conditions

Mild Traumatic Brain InjuryConcussion, MildConcussion, SevereConcussion, Intermediate

Interventions

RPM-assisted specialist access

OTHER

Contacts

Melissa Godfrey

CONTACT

267-425-0386 godfreym2@chop.edu

Auditory Plasticity Training

NCT06628505

Mild Traumatic Brain Injury

View study

RECRUITINGNA

Wearable Technology to Characterize and Treat mTBI Subtypes: Biofeedback-Based Precision Rehabilitation

NCT06381674

Mild Traumatic Brain Injury, ConcussionRehabilitation+1 more

View study

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: June 20, 2025Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions

Facilitating Access to Specialty Treatment

Inclusion Criteria

Exclusion Criteria

Auditory Plasticity Training

Wearable Technology to Characterize and Treat mTBI Subtypes: Biofeedback-Based Precision Rehabilitation

Integrating Metabolism, Connectivity, and Mesoscale Imaging at Ultra-high Field to Decipher Mechanisms of Resilience and Neurodegeneration in Neurological Diseases and Healthy Aging

MindRhythm Detection of Concussion and Recovery Study

Randomized Controlled Trial of Treatment to Optimize Heart Rate Variability for Persistent Post-Concussion Symptoms

BCAAs in Concussion 2.0