RecruitingNot ApplicableNCT05555771

Paediatric Syncope in the Emergency Department

Determining the Effectiveness of Counterpressure Maneuvers in Pediatric Patients Presenting With Syncope to the Emergency Department


Sponsor

Dr. Victoria Claydon

Enrollment

300 participants

Start Date

Sep 3, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

The investigators will assess the efficacy of clinically recommended counterpressure maneuvers (CPM) in preventing syncope for paediatric patients. Participants presenting to the emergency department (ED) will first provide written informed consent. In stage I, they will be asked to complete a brief survey documenting the presentation of their syncopal episode, and any prodromal symptoms they experienced. Participants that consent to the second stage of the study will either receive usual care (control arm) or training in counter pressure maneuvers alongside usual care (intervention arm; leg crossing, bending, arm tensing). These patients will be followed for one years time, and will be asked to complete monthly surveys detailing their syncopal and presyncopal recurrence. Medical records will be accessed over the duration of the study to identify any changes in medical diagnosis.


Eligibility

Min Age: 6 YearsMax Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is looking at children and teenagers who have a brief fainting episode (syncope) and come to the emergency department. Fainting in children is very common and usually benign, but it can sometimes signal a serious underlying heart or brain condition. The study aims to develop better tools to quickly identify which children are at low risk (and can safely go home) versus those who need further evaluation — reducing unnecessary testing while keeping patients safe. You may be eligible if: - Your child is between 6 and 18 years old - Your child had a brief episode of loss of consciousness that fully resolved and occurred within the last week - You present to the ED between 10am and 10pm - You and your child are willing to complete a survey in English You may NOT be eligible if: - Your child has a known cardiac arrhythmia such as Wolff-Parkinson-White or long QT syndrome - Your child has a history of traumatic head injury - Your child is presenting with a new seizure or recurrence of epilepsy - Your child was involved in a drug overdose or intoxication - Your child has structural heart disease - Your child has already been enrolled in this study previously Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALCounterpressure Maneuvers

Movements that can aid in delaying or preventing syncope by recruiting skeletal muscle pumping (via compression of major veins by contracting muscle to eject blood through cardiovascular circuit) and increased sympathetic drive (via sustaining an isometric muscle contraction). In this trial, we will be evaluating three commonly recommended maneuvers of arm tensing, squatting, and leg crossing with arm tensing. Maneuvers should be held for 1-2 minutes, or until symptoms subside.

BEHAVIORALUsual Care

Participants will engage in behavioural interventions and avoidance measures that are commonly recommended as a part of usual care for recurrent syncope. This primarily includes recommendations such as staying hydrated, increasing salt intake, avoiding warm temperatures, avoiding standing for long periods of time, and engaging in regular physical activity. Some patients may be prescribed medication (Midodrine, Fludrocortisone), or other assistive interventions (e.g., compression stockings) at the discretion of their physician.


Locations(1)

BC Children's Hospital

Vancouver, British Columbia, Canada

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NCT05555771


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