This is a double-blind, placebo-controlled, parallel group study designed to assess the tolerability and efficacy of fsCBD and bsCBD, compared to a placebo control, to improve cognition and traumatic brain injury-related symptoms. If eligible for the study, subjects will be randomized to receive one of the conditions for 12 weeks.
To better understand the effects of hemp-derived CBD with and without a small amount of THC, we propose a Phase II randomized clinical trial (RCT) to examine the safety, tolerability, and clinical effects of Full Spectrum CBD (fsCBD, contains less than 0.3% THC) vs. Broad Spectrum CBD (bsCBD, does not contain THC), vs. a matching placebo in a population of patients with traumatic brain injury. This is a double-blind, placebo-controlled, parallel group study designed to assess the tolerability and efficacy of fsCBD and bsCBD, compared to a placebo control, to improve cognition and TBI-related symptoms such as anxiety, pain, depression, and sleep. If eligible for the study, subjects will be randomized to receive one of the conditions for 12 weeks. The initial Week 0 / Baseline visit will take place at the University of Colorado Anschutz Medical Campus. There will be in-person visits at Weeks 1, 6, and 12. Participants will be contacted remotely each remaining week during the 12-week period.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
43
The current study will directly test the hypothesis that a moderate dose of CBD leads to improvements in cognition, TBI-related symptoms, pain, sleep, depression, anxiety, and peripheral markers of inflammation and oxidative stress.
Placebo arm
University of Colorado Anschutz
Aurora, Colorado, United States
Change in Neuropsychiatric Symptoms
The effects of study treatment (CBD or placebo) on neuropsychiatric symptoms associated with TBI will be assessed by the Neurobehavioral Symptom Inventory (NSI)
Time frame: Week 0 to Week 12
Change in Cognition
The effects of study treatment (CBD or placebo) on attention, processing speed, working memory, long-term memory recall, and executive function will be assessed using the Trail Making Test; the Wechsler Adult Intelligence Scale-IV (WAIS-IV) Digit Span, Symbol Search, Coding, Letter-Number Sequencing; and HVLT delayed recall, to create domain scores used to inform an aggregate measure of cognition.
Time frame: Week 0 to Week 12
Change in Biomarkers of Inflammation
Circulating levels of cytokine proteins before and after will be measured using immunoassay before and after treatment
Time frame: Week 0 to Week 6, Week 0 to Week 12
Change in Biomarkers of Oxidative Stress
Circulating levels of cytokine proteins before and after will be measured using immunoassay before and after treatment
Time frame: Week 0 to Week 12
Change in Pain Intensity
PROMIS Pain Intensity 1a - A single-item measure of pain intensity. Average pain in the last 7 days is recorded on a scale of 1 - 10, with higher scores indicating higher pain levels.
Time frame: Week 0 to 12
Change in Anxiety
PROMIS Anxiety SF - An 8-item measure to rate subjective anxiety symptoms. Possible scores range from 1 - 5 with higher scores indicating worse anxiety symptoms.
Time frame: Week 0 to 12
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Change in Sleep Disturbance
PROMIS SF v10 Sleep Disturbance 4a - a 4-item measure assessing subjective sleep quality.
Time frame: Week 0 to Week 6, Week 0 to Week 12
Change in Quality of Life
The Short Form 36 will be used to measure quality of life.
Time frame: Week 0 to Week 12
Change in Depression
The Beck Depression Inventory II (BDI-II) will be used to measure depressive symptoms throughout the study.
Time frame: Week 0 to Week 12