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Evaluation of the Impact of a Dietary and Nutritional Intervention on Persistent Post-concussive Symptoms

Brain Injury Traumatic Mild

Concussions affect thousands of Canadians every year. Although the effects are usually temporary, 10-15% of adults experience persistent symptoms likely to last several weeks or even months. It is suggested that nutritional interventions should be considered in concussion management because nutrition can act on several mechanisms of brain injury. However, to date, no study has assessed the impact of dietary interventions on the recovery of people with persistent post-concussive symptoms.

This randomized controlled trial aims to determine the impact of a dietary and nutritional intervention on the physical, cognitive, behavioural and emotional symptoms of patients with persistent post-concussive symptoms in New Brunswick, Canada. Patients will be randomized to one of three groups: 1) dietary treatments and nutritional supplements (experimental group A), 2) nutritional supplements (experimental group B), and 3) physiotherapy treatments (control group). Patients in group A will receive four consultations with a dietitian over eight weeks, in addition to conventional physiotherapy treatments. These patients will receive nutritional counselling and omega-3, vitamin D and creatine supplements. Patients in group B will be prescribed the same supplements as those in group A by their doctor and receive physiotherapy treatments. Finally, patients in the control group will only receive physiotherapy treatments. Patient symptoms will be measured using a questionnaire constructed from tools commonly used in practice. This questionnaire will be completed at the first physiotherapy session and 2, 4 and 8 weeks after the start of the intervention.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    16 and up

Participation 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

Study Location

Universite de Moncton
Universite de Moncton
Moncton, New Brunswick
Canada

Contact Study Team

Backup Contact

Horia-Daniel Iancu, PhD

[email protected]
506-858-4000
Primary Contact

Stephanie Ward Chiasson, PhD, RD

[email protected]
506-858-4000
Study Sponsored By
Universite de Moncton
Participants Required
More Information
Study ID: NCT05589064