No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
13 – 18
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
210 (estimated)
Sponsor
Children's Hospital of Philadelphia · Other
Who this trial is looking for
This trial is looking for teenagers between 13 and 18 who have had a concussion within the last 72 hours. Participants will use a mobile app to report their symptoms and get connected with specialists for better care.
Are You a Good Fit for This Trial?
You may be able to join if
I am between 13 and 18 years old.
I have come to the Children's Hospital of Philadelphia within 72 hours of my head injury.
I have been diagnosed with a concussion according to the latest guidelines.
I own a smartphone.
I have a moderate to high risk for ongoing symptoms.
You may not be able to join if
I have a Glasgow Coma Scale score lower than 13.
I have any trauma to my legs.
I had a concussion in the past month.
I do not speak English.
I was admitted to the hospital after my head injury.
I have already taken part in this study.
I cannot complete the study procedures.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
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) …
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.
Trial Locations
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City
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Status
Eligibility Criteria
Inclusion Criteria for concussed subjects:
* 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 Concussio…
Inclusion Criteria for concussed subjects:
* 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)
Exclusion Criteria for concussed subjects:
* 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.
Inclusion Criteria for parents:
* Child meets the study eligibility criteria
Exclusion Criteria for parents:
* Non-English speaking
Inclusion Criteria for providers:
* ED or specialty provider caring for at least one patient via the mobile Health (mHealth)-facilitated care handoff strategy
Exclusion Criteria for providers:
* Non-English speaking
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