Effectiveness of Rehabilitation in Adults Suffering From Persistent Concussion Symptoms
Postconcussion Syndrome, Mild Traumatic Brain Injury
About this trial
This is an interventional treatment trial for Postconcussion Syndrome
Eligibility Criteria
Inclusion Criteria: 21-years and older meet the definition of postconcussion syndrome, which requires a participant to report any 3 symptoms or more (from an inclusive list of 40 most commonly reported persisting symptoms) lasting at least 1-month following the diagnosis of a concussion. Concussion was defined according to the 5th International Consensus Statement on Concussion in Sport. Have adequate language skills in English to read and take part in rehabilitation treatment program. Exclusion Criteria: In-patients at Toronto Rehabilitation Institute or any other affiliated University Health Network clinics. Participants will be excluded should their clinical examination be unremarkable for objective physical impairments, Have a chronic infectious disease, Uncontrolled hypertension, Other neurological disorders (not attributed to their primary diagnosis), Cancer treatment (other than basal cell carcinoma), craniotomy, or refractory subdural hematoma long-term use of psychoactive medications that would compromise their ability to comprehend and perform study activities, those with pacemakers or elevated cardiovascular risk, Ongoing litigation surrounding their injury, Have been diagnosed with a moderate or severe brain injury prior to enrolment, post-concussive symptoms persisting beyond 12-months.
Sites / Locations
- Toronto Rehabilitation InstituteRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Individualized care program
Usual care
Participants in the individualized care stream, will be provided reassurance and psychoeducation via the bio-psycho-social model on understanding persistent symptoms consistent with usual care. Additionally, they will be afforded up to 12 treatments over the course of 6-weeks. Treatments will be standardized; however, given the heterogeneity of symptoms, components of the treatments will be individualized to the participants based on what subgroup they're classified into at baseline based on their initial clinical examination and self-reported dominant impairment. Regardless of subgroup classification, as part of individualized care, all patients will receive reassurance and psychoeducation about the bio-psycho-social understanding of persistent symptoms, including advice on adaptive illness behaviours, such as gradually resuming premorbid activities and avoiding excessive rest and "all-or-nothing behaviour".
Active control - All participants in the active control group will receive 'usual care', (twice a week for 6 weeks), which will consist of reassurance and psychoeducation via the bio-psycho-social model on understanding persistent symptoms, including advice on adaptive illness behaviours, such as gradually resuming premorbid activities and avoiding excessive rest and "all-or-nothing behaviour". Additionally, participants will be afforded weekly 20-minute supervised progressive sub-symptom aerobic exercise sessions at the KITE clinic under the supervision of study coordinator. They will be instructed to also perform daily 20-minutes of subsymptom aerobic exercise outside the supervised exercise sessions.