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Cognitive Rehabilitation for Concussion
N/A
Waitlist Available
Led By Noah Silverberg, PhD
Research Sponsored by University of British Columbia
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Age 18-59 years old
Age 18-65 years old
Must not have
Unstable/serious medical condition (e.g., cancer, multiple sclerosis, etc.),
Timeline
Screening 3 weeks
Treatment Varies
Follow Up week 12
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a new therapy to help people with long-term memory problems after a concussion. It focuses on changing negative thoughts about memory. The study targets those who had a concussion within the past few months to a couple of years and still have memory issues. The goal is to see if this therapy is practical and effective.
Who is the study for?
This trial is for adults aged 18-65 who had a concussion 6-24 months ago, meet criteria for Functional Cognitive Disorder, speak English fluently, and have regular internet access. It's not for those with serious conditions like cancer or MS, MRI contraindications, failed validity tests, severe mental illness requiring recent hospitalization, substance abuse disorders, or on memory-impairing meds.
What is being tested?
The study is testing a new cognitive behavioural therapy (CBT) aimed at improving memory after a concussion. Participants will be randomly assigned to either this CBT or an alternative cognitive rehabilitation program to compare effectiveness. The focus is on how feasible the treatment is based on recruitment success and participant adherence.
What are the potential side effects?
Since the interventions are non-medical therapies (CBT and cognitive rehabilitation), they typically do not have side effects like drugs do. However, participants may experience emotional discomfort discussing their experiences during sessions.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am between 18 and 59 years old.
Select...
I am between 18 and 65 years old.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I do not have any serious or unstable medical conditions.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ week 12
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~week 12
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Memory concern
Patient adherence
Recruitment
+3 moreSecondary study objectives
Avoidance
Catastrophization
Patient Global Impression of Change
+1 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Cognitive Behavioural Therapy (CBT)Experimental Treatment1 Intervention
11 weekly sessions of cognitive behavioural therapy (CBT) delivered over videoconference
Group II: Cognitive RehabilitationActive Control1 Intervention
11 weekly sessions of traditional cognitive rehabilitation delivered over videoconference
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Cognitive Behavioural Therapy (CBT)
2017
N/A
~970
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Cognitive Behavioral Therapy (CBT) is a common treatment for concussion that focuses on improving functional memory symptoms through cognitive and behavioral techniques. The mechanism of action involves helping patients develop strategies to manage and compensate for memory deficits, enhancing their cognitive control, and reducing the psychological impact of memory problems.
This is crucial for concussion patients as it not only aids in the recovery of cognitive functions but also helps in managing associated emotional and psychological stress, thereby improving overall quality of life.
Find a Location
Who is running the clinical trial?
University of British ColumbiaLead Sponsor
1,465 Previous Clinical Trials
2,485,467 Total Patients Enrolled
Harvard Medical School (HMS and HSDM)OTHER
203 Previous Clinical Trials
1,316,429 Total Patients Enrolled
Noah Silverberg, PhDPrincipal InvestigatorUniversity of British Columbia
5 Previous Clinical Trials
474 Total Patients Enrolled
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