Actively Recruiting

Phase Not Applicable
Age: 6Years - 18Years
All Genders
ID05633693

Impact of Postural Sway on Cardiovascular Control in Pediatric Patients With Syncope

Led by Simon Fraser University · Updated on 2026-04-23

30

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

Sponsors

S

Simon Fraser University

Lead Sponsor

P

Provincial Health Services Authority British Columbia

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating whether specific muscle movements in the lower body, called discrete counterpressure maneuvers (CPM), can improve blood pressure and heart function in children aged 6 to 18 years who experience fainting. The study focuses on children with recurrent fainting due to vasovagal syncope or postural orthostatic tachycardia syndrome (POTS). Researchers will compare cardiovascular responses to different maneuvers and analyze factors like sex, puberty stage, body size, and autonomic nervous system control. Participants will perform a series of movements including leg crossing with muscle tensing, crouching, exaggerated forward-backward swaying, and rhythmic gluteal muscle clenching. These maneuvers will be tested alongside a baseline standing period, with volunteers acting as their own controls. The study involves one 1.5-hour session where participants will undergo cardiovascular monitoring using non-invasive devices measuring heart rate, blood pressure, cerebral blood flow, and stroke volume. Tests include the Valsalva maneuver and sit-stand transitions. During the session, participants will complete questionnaires on fainting history, physical activity, and quality of life. Measurements of height, weight, muscle mass, and pubertal development will be taken. Urine samples will be collected briefly for sodium testing. Continuous cardiovascular data will be recorded during rest, standing, and maneuver performance. The main outcome is how stroke volume relates to postural movements. Safety will be monitored closely, and testing will pause if participants feel unwell. The total participation time is about 1.5 hours in a controlled clinical setting.

CONDITIONS

Brief Title

Postural Sway and Counterpressure Maneuvers for Pediatric Syncope

Who Can Participate

Age: 6Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • English-speaking children aged 6 to 18 years
  • Diagnosed with recurrent fainting (at least two episodes in the last year) due to vasovagal syncope or postural orthostatic tachycardia syndrome (POTS)
  • Willing to attend one testing session
  • Able to complete testing procedures and questionnaires
Not Eligible

You will not qualify if you...

  • Diagnosed with cardiac arrhythmias such as Wolff-Parkinson-White or Long QT syndrome
  • History of traumatic head injury
  • New or recurrent seizure disorder or epilepsy
  • Overdose or intoxication history
  • Structural heart disease or cardiovascular diseases including hypertension, diabetes, or renal disease
  • Hypoglycemia
  • Physical or psychological disabilities that prevent test completion
  • Pregnant or possibly pregnant females
  • Taking cardiovascular acting medications including treatments for orthostatic syncope
  • Not fully vaccinated against COVID-19 as per current guidelines

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Approximately 1.5 hours

Participants attend one testing session involving various cardiovascular and postural assessments, including performing counterpressure maneuvers and baseline standing trials while cardiovascular responses are monitored using non-invasive equipment.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Simon Fraser University

Burnaby, British Columbia, Canada, V5A1S6

Actively Recruiting

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Research Team

E

Erin L Williams, BSc

V

Victoria E Claydon, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Counter pressure maneuvers for syncope prevention: A semi-systematic review and meta-analysis.

Erin Lori Williams, Farhaan Muhammad Khan, Victoria Elizabeth Claydon

https://pubmed.ncbi.nlm.nih.gov/36312294

Decreased skeletal muscle pump activity in patients with postural tachycardia syndrome and low peripheral blood flow.

Julian M Stewart, Marvin S Medow, Leslie D Montgomery...

https://pubmed.ncbi.nlm.nih.gov/14576081

Effectiveness of physical counterpressure maneuvers in preventing vasovagal syncope: the Physical Counterpressure Manoeuvres Trial (PC-Trial).

Nynke van Dijk, Fabio Quartieri, Jean-Jaques Blanc...

https://pubmed.ncbi.nlm.nih.gov/17045903

Pubertal Hormonal Changes and the Autonomic Nervous System: Potential Role in Pediatric Orthostatic Intolerance.

Kassandra E Coupal, Natalie D Heeney, Brooke C D Hockin...

https://pubmed.ncbi.nlm.nih.gov/31798399