Impact of a Paced Breathing Exercise Intervention on Autonomic Nervous System Function After Pediatric Concussion

Recruiting N/A Interventional Study
Concussion, Mild
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
9 – 18
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
20 (estimated)
Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre · Other
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About This Trial
The goal of this pilot clinical trial is to assess the feasibility of administering a paced breathing exercise intervention program to children and adolescents in the sub-acute period after concussion, and to document the autonomic function, and symptom severity (post-concussion symptoms, anxiety, sleep) before and after administration of the intervention. Participants will: will be instructed t…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * aged 9-18 years * seven days-3 months post-concussion, * at least one post-concussion symptom in the Post-concussion Symptom Inventory (PSCI) that is relevant to ANS dysfunction (e.g. dizziness, nausea, fatigue, confusion, anxiety or sleep disturbances). Exclusion Criteria: …
Contacts

Isabelle Gagnon, PhD

514-412-4400

isabelle.gagnon8@mcgill.ca

CONTACT