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.
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:
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Contacts