Traumatic Brain Injury
Research Study
This study is testing whether light therapy can help older adults with a past non-penetrating traumatic brain injury (a TBI that did not break the skull). Researchers want to see if the therapy improves blood flow in the brain, thinking skills, and if it causes any side effects.
Fast Facts
Experienced a traumatic brain injury (TBI) 6 months to 10 years ago
TBI was non-penetrating (did not break the skull)
Ages 40-85
Compensation
up to $1250
Conducted in
Manhattan, NYC
Additional Information
This study is focused on a type of light therapy called transcranial photobiomodulation (tPBM), in which near-infrared energy is applied to the forehead. Near infrared energy is like light but is not visible to the human eye.
We want to find out whether this type of therapy can change blood flow in the brains of people with traumatic brain injury and improve their functioning. Eventually, the findings of this study may provide better treatment options for people living with the effects of TBI.
You may be eligible for this study if you meet the following criteria.
Inclusion Criteria:
- Ages 40-85
- Experienced a traumatic brain injury (TBI) 6 months to 10 years ago
- TBI was non-penetrating (injury did not break the skull)
- TBI was considered moderate in severity
- Able to undergo an MRI (no claustrophobia or non-removable objects in the body)
- No history of dementia or other serious neurological conditions
- Able to travel to Midtown Manhattan for study visits
There will be a total of 22 visits separated by phases, lasting about 20 weeks altogether. All visits are in person.
Phase 1: Screening and Enrollment (4-6 hours)
- Consent
- Neuropsychological testing
- Questionnaires
- Blood draw
- Urine drug testing
Phase 2: Baseline phase (3-5 hours)
- MRI of the brain
- You will receive both the treatment and a “sham” procedure with the light therapy device.
Phase 3: Treatment phase (25-27 hours of participation across 18 visits)
- You will be randomly placed into either the treatment or the “sham” group. You won’t know which group you are in and the investigators will not know either.
- For 6 weeks, you will come 3 days a week (a total of 18 visits) and have either sham or treatment, depending on which group you were randomly assigned.
Phase 4: Primary outcome phase (5-8 hours) over one week
- MRI of the brain
- Neuropsychological testing
- Questionnaires
Phase 5: Follow up phase (4-5 hours)
- 8 weeks post-treatment
- Neuropsychological testing
- Questionnaires
Participants may receive up to $1,250 in compensation for their time and effort.
There is no cost for you to participate in our research study.