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Clinical Trials/NCT01873287
NCT01873287
Completed
Not Applicable

Predicting Persistent Postconcussive Problems in Pediatrics: A Clinical Prediction Rule Derivation and Validation Study

Children's Hospital of Eastern Ontario9 sites in 1 country3,063 target enrollmentAugust 2013
ConditionsConcussionsPCS

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Concussions
Sponsor
Children's Hospital of Eastern Ontario
Enrollment
3063
Locations
9
Primary Endpoint
Count of Children Who Have Persistent Post-concussive Symptoms (PCS) at One-month Follow-up.
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Concussion, a mild traumatic injury common in children and adolescents, is a complex pathophysiological process affecting the brain. The lay press is inundated with reports of tragic consequences of concussion, and children are not immune.

Persistent postconcussive symptoms (PCS) is defined as the persistence of somatic, cognitive, physical, psychological or behavioural changes lasting more than one month following injury. PCS significantly impacts children and their family's quality of life through school absenteeism, depressed mood and loss of activities.

Validated, easy-to-use prognosticators do not exist for clinicians to identify children at highest risk for PCS. As a result,physicians cannot accurately inform children and parents whether they should expect longer symptoms, nor initiate pharmacotherapy or other management to reduce the occurrence or severity of PCS.

The investigators objective is to derive and validate a clinical prediction rule for the development of PCS in children and adolescents presenting to the emergency department (ED) following acute head injury. The investigators have three aims: (1) determine PCS incidence at one-month follow-up in children aged 5-17 who sustain a concussion; (2) derive a rule to predict PCS from variables present in the history and physical examination; and, (3) assess the accuracy, reliability and acceptability of the prediction rule in a subsequent cohort. Using a prospective, multicentre study at nine large Canadian pediatric EDs, the investigators will recruit the largest prospective epidemiological cohort of children with concussions in the literature.

This work will provide rigorous evidence to determine PCS incidence in children and its impact on quality of life. The results will enable clinicians to identify children at highest risk for PCS, optimize treatment and provide families with realistic anticipatory guidance. This study will also establish a strong and vital evidence base to advance concussion research.

Detailed Description

The full protocol has been published in BMJ Open (open access): Zemek R, Osmond MH, Barrowman N for PERC Concussion Team. Predicting and preventing postconcussive problems in paediatrics (5P) study: protocol for a prospective multicentre clinical prediction rule derivation study in children with concussion. BMJ Open. 2013 Aug 1;3(8). pii:e003550. doi: 10.1136/bmjopen-2013-003550. PubMed PMID: 23906960. https://www.ncbi.nlm.nih.gov/pubmed/23906960 The primary outcome results have been published in JAMA (open access): Zemek R, Barrowman N, Freedman SB, Gravel J, Gagnon I, McGahern C, Aglipay M, Sangha G, Boutis K, Beer D, Craig W, Burns E, Farion KJ, Mikrogianakis A, Barlow K, Dubrovsky AS, Meeuwisse W, Gioia G, Meehan WP 3rd, Beauchamp MH, Kamil Y, Grool AM, Hoshizaki B, Anderson P, Brooks BL, Yeates KO, Vassilyadi M, Klassen T, Keightley M, Richer L, DeMatteo C, Osmond MH; Pediatric Emergency Research Canada (PERC) Concussion Team. Clinical Risk Score for Persistent Postconcussion Symptoms among Children With Acute Concussion in the ED. JAMA. 2016 Mar 8;315(10):1014-25. doi: 10.1001/jama.2016.1203. PubMed PMID: 26954410. http://dx.doi.org/10.1001/jama.2016.1203

Registry
clinicaltrials.gov
Start Date
August 2013
End Date
June 2015
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Roger Zemek

Pediatric Emergentologist, Division of Emergency Medicine

Children's Hospital of Eastern Ontario

Eligibility Criteria

Inclusion Criteria

  • Subjects presenting to one of the study hospital EDs after sustaining a head injury will be eligible if they:
  • are aged 5 to 17 years;
  • have a concussion, defined by Zurich consensus statement;22
  • suffered the initial injury in the previous 48 hours;
  • are proficient in English or French.

Exclusion Criteria

  • Patients will be excluded if they present with traumatic head injuries with any of the following:
  • GCS ≤13; any abnormality on standard neuroimaging studies, including any positive head CT findings (Note: neuroimaging is not required, but may be performed by the clinician if thought to be clinically indicated);
  • neurosurgical operative intervention, intubation or PICU care required;
  • multi-system injuries with treatment requiring admission to hospital, operating room or procedural sedation in the ED (Note: admission to hospital for observation or management of ongoing concussion symptoms is not an exclusion criteria);
  • severe chronic neurological developmental delay resulting in communication difficulties;
  • intoxication at the time of ED presentation as per clinician judgment;
  • no clear history of trauma as primary event (e.g., seizure, syncope or migraine as primary event);
  • previously enrolled in this same study.

Outcomes

Primary Outcomes

Count of Children Who Have Persistent Post-concussive Symptoms (PCS) at One-month Follow-up.

Time Frame: 1 month

The primary outcome is the number of of children aged 5 - 17 years who have PCS at one-month follow-up. A PCS case is defined as an increase from pre-concussion baseline of three or more symptoms on the validated PCSI at one-month (consistent with the ICD-10 definition of PCS).

Secondary Outcomes

  • Neuropsychological Evaluation(1 month and 3 month)
  • Pediatric Quality of Life Inventory (PedsQL) Total Score at 4-weeks Post-injury(1 month)

Study Sites (9)

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