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SMART Concussion Trial: Symptom Management vs Alternative Randomized Treatment of Concussion Trial

Mild Traumatic Brain Injury | Neck Pain | Dizziness | Headaches Posttraumatic

Given the rising rates of concussion in youth ages 10-19 and the significant proportion of young people who remain symptomatic for months following concussion, research evaluating the efficacy of multifaceted treatment options following concussion is imperative. Studies examining the efficacy of treatment strategies following concussion in children and adults are surprisingly limited, and most focus on one treatment approach, have small sample sizes, are not randomized controlled trials, and focus on individuals with prolonged recovery (months). There is a need for a multifaceted treatment trial to examine the early implementation of treatment approaches that may reduce prolonged recovery while considering the heterogeneous presentation of symptoms and patient preferences in the sub-acute stage following concussion. Randomized controlled trials that consider a multifaceted transdisciplinary approach to treatment in the early period following concussion are needed to raise the bar regarding evidence-informed management following concussion

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Participation Requirements

  • Sex:

    ALL

  • Eligible Ages:

    13 to 19

Participation Criteria

Inclusion Criteria:

* 13 - 19 years of age at the start of treatment
* Diagnosed by the study physician with a concussion as per the 5th International Consensus Statement on Concussion in Sport1
* Glasgow Coma Scale 13-15 if recorded
* Loss of consciousness \< 30 minutes if present
* Post-traumatic amnesia \< 24 hours if present
* Diagnosis within 2 weeks of injury
* Moderate-severe symptoms of dizziness, neck pain, headaches, or sleep disturbance at \> one week and \< three weeks post injury reported on the PCSS (3-6 on 0-6 Likert scale for at least one of three symptoms)
* Patients can have a history of migraine or a family history of migraine

Exclusion Criteria:

* Inability to communicate orally and/or in writing in English language
* Significant developmental delay or intellectual disability
* No access to smartphone or computer
* Red flags or other clinical indication suggesting that further medical investigation is warranted (e.g., neurological scan - reflexes, dermatomes, myotomes, long tract signs, CN II-XII, Cerebellar Scan
* Unresolved Benign Paroxysmal Positional Vertigo (BPPV) (Dix-Hallpike and Roll Test)
* Inability to participate in physical activity for a reason other than concussion
* Orthopedic or other injury precluding ability to participate
* Medical history of neurological conditions: seizures (febrile SZ will be allowed), stroke, previous moderate/severe TBI, CNS cancers, SCI
* Psychotic disorder
* Inability to provide informed consent
* History of surgery in the occipital region
* Uncontrolled rheumatologic, inflammatory, or neurologic disorders (eg MS); Fibromyalgia/chronic fatigue syndrome; coagulopathy; immunosuppression
* Active cancer
* Herpes zoster infection in last 6 months
* Pregnancy
* Steroid injection to the greater or lesser occipital nerve infiltration in past 3 months
* Previously enrolled in the trial

Study Location

University of Calgary
University of Calgary
Calgary, Alberta
Canada

Contact Study Team

Backup Contact

Lisa Marie Langevin, PhD

4039557254
Primary Contact

Heather Godfrey, BSc, BN

4039552797
Study Sponsored By
University of Calgary
Participants Required
More Information
Study ID: NCT05446597