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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05365776
Other study ID # H21-02605
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 1, 2022
Est. completion date August 2024

Study information

Verified date May 2024
Source University of British Columbia
Contact Noah Silverberg, PhD
Phone 16047341313
Email noah.silverberg@ubc.ca
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Concussions are very common. Although many people recover well from concussion, some will have persistent symptoms and difficulties with daily activities. How people cope with their symptoms following concussion powerfully influences their recovery. Fear avoidance behaviour is a particularly unhelpful approach to coping, in which people perceive their pre-injury activities as unnecessarily dangerous and take great care to avoid overexertion and overstimulation. The investigators developed and pilot tested a behavioural therapy, called graded exposure therapy, to reduce fear avoidance behaviour. Our preliminary work suggested that graded exposure therapy was acceptable to patients with concussion and possibly beneficial for their recovery. The GET FAB after concussion study will assess the effectiveness of graded exposure therapy.


Description:

GET FAB is a multisite randomized controlled trial designed to evaluate a behavioural treatment (graded exposure therapy) for adults with persistent symptoms after concussion. Participants in this study will be recruited from a network of concussion clinics in Canada. This study follows from the investigators' prior work establishing that (1) fear avoidance behaviour is a risk factor for poor concussion outcome, (2) graded exposure therapy reduces fear avoidance behaviour, and (3) graded exposure therapy is perceived as credible and is well-tolerated by patients with persistent post-concussion symptoms. Participants will be assigned at random (in a 1:2:2 ratio) to receive enhanced usual care, graded exposure therapy group, or another therapy that might have similar benefits (prescribed aerobic exercise). The investigators hypothesize that patients who participate in graded exposure therapy will have reduced fear avoidance behaviour and improved daily functioning compared to other treatment conditions and this difference will be greatest for patients who enter the study with high fear avoidance behaviour.


Recruitment information / eligibility

Status Recruiting
Enrollment 220
Est. completion date August 2024
Est. primary completion date August 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 69 Years
Eligibility Inclusion Criteria: 1. aged 18-70 years; 2. sustained a concussion according to the ACRM mTBI Task Force definition between 1 and 24 months ago 3. fluent in English, because validated translations are not available for most questionnaires and recruiting multilingual therapists is not feasible; 4. access to a computer, tablet, or smartphone with internet capability; 5. 3 or more moderate-severe symptoms on the Rivermead Postconcussion Symptom Questionnaire. Exclusion Criteria: 1. medical contraindication to aerobic exercise (cardiac disease, chest pain with exertion, acute bone/joint/soft tissue injury aggravated by exercise) 2. change in cardiac medication within the last month, such as beta blockers, calcium channel blockers, or ivabradine 3. involved in personal injury litigation for index mTBI 4. currently pregnant or plan to become pregnant within the next three months 5. severe/unstable medical or psychiatric condition that could worsen over the next year")

Study Design


Intervention

Behavioral:
Graded Exposure Therapy
Graded exposure therapy is delivered by a psychologist over 12 individual (1:1) secure videoconference sessions. The core active ingredient is graded situational exposure to foster habituation and challenge beliefs that the avoided activities are dangerous. Homework exercises involve planned exposure exercises in the home and community to support generalization.
Prescribed aerobic exercise
Participants will be asked to complete 30 minutes of aerobic exercise on 5 days/week for a 12-week period. Participants select the mode (e.g., swimming, jogging, bicycling) and location of exercise (e.g., outdoors, a gym or community centre, at home). The initial exercise intensity target will be based on the Buffalo Concussion Bike Test. The target progression will be 3-5 beats per minute every two weeks.
Other:
Enhanced usual care
Usual care (education about concussion from the website: concussion.vch.ca/) will be enhanced through email message support.

Locations

Country Name City State
Canada Calgary Brain Injury Program Calgary Alberta
Canada Fraser Health Acquired Brain Injury and Concussion Services Langley British Columbia
Canada Head Injury Clinic at St. Michael's Toronto Ontario
Canada Hull-Ellis Concussion and Research Clinic Toronto Ontario
Canada Sunnybrooke Traumatic Brain Injury Clinic Toronto Ontario
Canada Toronto Western Hospital Toronto Ontario
Canada G.F. Strong Adult Concussion Services Vancouver British Columbia

Sponsors (2)

Lead Sponsor Collaborator
University of British Columbia Canadian Institutes of Health Research (CIHR)

Country where clinical trial is conducted

Canada, 

References & Publications (1)

Silverberg ND, Cairncross M, Brasher PMA, Vranceanu AM, Snell DL, Yeates KO, Panenka WJ, Iverson GL, Debert CT, Bayley MT, Hunt C, Baker A, Burke MJ; Canadian Traumatic Brain Injury Research Consortium (CTRC). Feasibility of Concussion Rehabilitation Approaches Tailored to Psychological Coping Styles: A Randomized Controlled Trial. Arch Phys Med Rehabil. 2022 Aug;103(8):1565-1573.e2. doi: 10.1016/j.apmr.2021.12.005. Epub 2021 Dec 28. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other World Health Organization Disability Assessment Schedule (WHODAS) 2.0 12-item: interviewer version: Change. score of 12 to 60, where higher scores indicate higher disability or loss of function 3 months
Other The Generalized Anxiety Disorder-7 score of 0-15, where higher scores indicate severity of anxiety experienced. 3 months
Other Personal Health Questionnaire-9 score of 0-27, where higher scores indicate severity of depression experienced. 3 months
Other The Post-Concussion Functional Scale-Screen 0 (unable) - 5 (more than 2 hours), higher score means longer length of time an activity can be tolerated without symptoms. baseline and 3 months
Primary Rivermead Post Concussion Symptoms Questionnaire (RPQ): Change Score of 0-64, with a higher score indicates worse symptoms. 3 months
Secondary Fear Avoidance Behaviour after Traumatic Brain Injury Questionnaire (FAB-TBI): Change score of 0-48, where higher score indicates higher avoidance. 3 months
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