Impact of dietary and nutritional intervention on post-concussive symptoms
Evaluation of the Impact of a Dietary and Nutritional Intervention on the Physical, Cognitive, Behavioural and Emotional Symptoms of Patients With Persistent Post-concussive Symptoms
This study is testing whether changes in diet and nutrition can help people with ongoing concussion symptoms feel better compared to those getting just supplements or physiotherapy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 120 (estimated) |
| Ages | 16 Years and up |
| Sex | All |
| Sponsor | Universite de Moncton Academic / other |
| Locations | 1 site (Moncton, New Brunswick) |
| Trial ID | NCT05589064 on ClinicalTrials.gov |
What this trial studies
This randomized controlled trial evaluates how dietary and nutritional interventions can affect the recovery of patients experiencing persistent post-concussive symptoms. Participants will be divided into three groups: one receiving dietary treatments and nutritional supplements, another receiving only nutritional supplements, and a control group receiving physiotherapy treatments. The study aims to assess changes in physical, cognitive, behavioral, and emotional symptoms over time. Conducted in New Brunswick, Canada, this trial seeks to explore a novel approach to concussion management through nutrition.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 16 and older who have experienced persistent post-concussive symptoms for at least 2 weeks but no longer than 6 months.
Not a fit: Patients under 16 years old, those with neurological disorders, or individuals in the acute phase of inflammatory bowel disease may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could provide a new, effective strategy for alleviating persistent post-concussive symptoms in patients.
How similar studies have performed: While some studies have explored nutritional supplements for brain injury recovery, this specific approach to dietary intervention for persistent post-concussive symptoms is novel and has not been previously tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 16 years or older * Must be able to understand English or French * Have persistent post-concussive symptoms lasting at least 2 weeks but no longer than 6 months Exclusion Criteria: * \<16 years old * People who are breastfeeding, pregnant or plan to become pregnant in the next 2 months * People with neurological disorders (other than concussion) or a history of moderate or severe brain injury * People in an acute phase of an inflammatory bowel disease * Any physical condition prohibiting a patient from receiving physiotherapy treatments
Where this trial is running
Moncton, New Brunswick
- Universite de Moncton — Moncton, New Brunswick, Canada (Recruiting)
Study contacts
- Principal investigator: Stephanie Ward Chiasson, PhD, RD — Universite de Moncton
- Study coordinator: Stephanie Ward Chiasson, PhD, RD
- Email: stephanie.ward@umoncton.ca
- Phone: 506-858-4000
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.