Percutaneous Electrical Nerve Field Stimulation (PENFS) in Patients With Post Concussion Syndrome (PCS)
Recruiting
N/A
Interventional Study
Post-Concussion Syndrome
COVID Long-Haul
COVID-19
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 11 – 18
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 125 (estimated)
- Sponsor
- Children's Hospital of Orange County · Other
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About This Trial
The purpose of this study is to test the effect of Auricular Percutaneous Electrical Nerve Field Stimulation (a Neurostim device) on children with pain and Post Concussion symptoms. An additional purpose of this study is to demonstrate that PENFS improves functioning in children with post Covid-19 symptoms.
Trial Locations
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Eligibility Criteria
Concussion:
Inclusion Criteria:
* Clinical diagnosis of Post-Concussion Syndrome
* Post-Concussion Symptoms for at least 3 months along with lack of other explanation for their symptoms
* English and Spanish-speaking families
Exclusion Criteria:
* Seizure disorders
* Significant developmental de…
Contacts