Improving memory symptoms after brain concussion
Official title: REhabilitation of MEMory Symptoms After BRain Concussion
Run by University of British Columbia · NCT06956417 · Data updated 2026-11-12
This study is testing whether cognitive behavioral therapy or memory training can help adults who have ongoing memory problems after a concussion feel better.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 59 Years |
| Sex | All |
| Enrollment | 184 (estimated) |
| Sponsor | University of British Columbia Academic / other |
| Locations | 8 sites (Calgary, Alberta and 7 other locations) |
| Status | Recruiting |
| Started | July 2, 2025 |
| Main results expected | April 30, 2028 |
| Study ends | April 30, 2029 |
| Registry record updated | June 2, 2026 |
| Trial ID | NCT06956417 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults aged 18-59 who have experienced a concussion within the last 6 to 36 months and are experiencing ongoing memory concerns.
✕Probably not a fit
Patients with comorbid psychiatric or neurological disorders or those whose memory symptoms can be fully explained by medication will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to evaluate the effectiveness of cognitive behavioral therapy (CBT) and cognitive compensatory strategy training (CCST) in improving subjective memory functioning in adults who have persistent memory symptoms following a concussion. Participants will be randomly assigned to one of three groups: CBT, CCST, or a waitlist control. The study will utilize a multisite, three-armed randomized control trial design, ensuring that participants are blinded to the other treatment arms. The goal is to determine which intervention is most effective in addressing memory concerns after a concussion.
Why it matters
Potential benefit: If successful, this study could provide effective therapeutic options for individuals suffering from persistent memory issues after a concussion.
How similar studies have gone: Previous studies have shown promise in using cognitive rehabilitation and CBT for memory improvement, suggesting that this approach may be effective.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Age 18-59 2. Concussion diagnosis confirmed with structured interview based on American Congress of Rehabilitation Medicine diagnostic criteria 3. Concussion occurred between 6 and 36 months before enrollment 4. Ongoing memory concerns 5. Fluent in English 6. Stable access to a computer, tablet, or smartphone with internet capability Exclusion Criteria: 1. Fail performance validity testing 2. Comorbid psychiatric or neurological disorder or is taking a medication that could fully account for their memory symptoms
Where it's running
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Calgary Brain Injury Program
Calgary, Alberta, Canada Recruiting -
Fraser Health Acquired Brain Injury and Concussion Services
Langley, British Columbia, Canada Recruiting -
G.F. Strong Adult Concussion Services
Vancouver, British Columbia, Canada Recruiting -
360 Concussion Care Clinic
Ottawa, Ontario, Canada Recruiting -
Sunnybrook Traumatic Brain Injury Clinic
Toronto, Ontario, Canada Recruiting -
Hull-Ellis Concussion and Research Clinic at University Health Network
Toronto, Ontario, Canada Recruiting
Show 2 more locations
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Canadian Concussion Centre at Toronto Western Hospital
Toronto, Ontario, Canada Recruiting -
Integrated Adult Concussion Program at Hamilton Health Sciences
Hamilton, Ontario, Canada Active not recruiting
Study contacts
- Principal investigator: Noah D Silverberg, PhD — University of British Columbia
- Study coordinator: Noah D Silverberg, PhD
- Email: noah.silverberg@ubc.ca
- Phone: 6047341313
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.