- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04641832
The Combined Effect of Chronic Cannabis Use and Subconcussive Head Impacts on Brain Health
The Effect of Chronic Cannabis Use on Neural Response to Acute Subconcussive Head Impacts
Study Overview
Detailed Description
NUMBER OF PEOPLE TAKING PART IN THE STUDY
We plan to recruit 45 THC using subjects and 45 non-using subjects.
PROCEDURES FOR THE STUDY
Participants will be assigned to the THC cannabis user group or the nonuser group based on participants' report of past cannabis use. These groups will then be verified using saliva and urine tests for cannabis use history.
The study consists of 4 test sessions during a 4-day period. The 1st day will take approximately 4 hours. The 2nd and 4th day will each take approximately 1 hour. Participants will not need to do anything on the 3rd day.
- The 1st test session takes place right before the soccer heading intervention.
- After the 1st test session, participants will then perform 20 soccer headings in 10 minutes.
- The 2nd test session takes place 2h after the intervention.
- The 3rd test session takes place approximately 24h after the intervention.
- The 4th test session takes place approximately 72h after the intervention.
During each test session, participants will be asked to complete a paper-pencil questionnaire assessing participants' current feeling. The questionnaire consists of 22 possible symptoms with 7-point scale to see if participants are experiencing concussion-related symptoms. A trained phlebotomist will draw blood from a vein in participants' arm at the four time points described in the above bulletpoints. Each 4mL blood sample is equivalent to approximately 1 teaspoon. A total of approximately 16mL (3-4 teaspoons) will be drawn during this study. The researchers will collect saliva samples (2mL) at each time point. Participants will be then asked to perform eye-movement tasks with directions from the research assistant. The eye-movement tasks consist of watching an object nearing the face (called a convergence test) and a brief test that asks participants to name numbers aloud from a screen. These eye-movement tasks will be repeated twice and will take about 2 minutes. After eye-movement testing, the investigators will ask participants to complete an imPACT test, which is a computerized test commonly used to diagnose concussions that measures memory, attention span, and visual and verbal problem solving. Completing the imPACT takes 20 to 25min. The last test is an autonomic function test, where participants will place participants' hand in a bowl of ice water for 60s while participants' heartrate is recorded.
The first 1st test session is slightly longer than the other two. It requires a saliva collection, where participants are asked to collect saliva in his/her mouth for approximately 15s before spitting onto a test strip. Researchers will need to collect about 7mL (1.5 teaspoon) of saliva from participants. This test will verify that participants have not used cannabis products in the past 72 hours. participants will also be asked for a urine sample. A urine sample of approximately 50mL will be used to verify cannabis use history over the past 3 months.
During the 1st day, after finishing the 1st test session, participants will perform 20 soccer headings. A standard size 5 soccer ball will be projected at 25 mph (equivalent speed to a long throw-in) by a JUGS soccer machine, and participants will perform 20 headers with 30 seconds resting period between each header. participants will be asked to direct the ball back towards the JUGS soccer machine in the air.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Indiana
-
Bloomington, Indiana, United States, 47405
- Indiana University School of Public Health
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
For Chronic THC User Group
- being between 18 to 26 years of age
- self-reported chronic THC use (average use once per week but not dependent)3) at least 3 years of soccer heading experience.
For Non-User Cohort
- being between 18 to 26 years of age
- self-reported non cannabis use in the past 6 months
- at least 3 years of soccer heading experience
Exclusion Criteria:
- any head, neck, or face injury in the 1 year prior to the study (e.g., concussion, eye injury);
- history of vestibular, ocular, or vision dysfunction (e.g., macular degeneration)
- currently taking any medications affecting balance (e.g., antibiotics)
- pregnancy
- HIV
- any neurological disorders (e.g., seizure disorders, closed head injuries with loss of consciousness greater than 15 minutes, CNS neoplasm, spinal cord injury/surgery, history of stroke)
- hypertension, cardiac arrhythmia, or pulmonary disease
- lower extremity injury that would prohibit performing soccer headings
metal implants in the head
Session-specific exclusion criteria will include:
- used cannabis within the last 72 hours (verified by saliva cannabis test before intervention)
- slept less than 4 hours before the 1st and 2nd test day (verified by screening questionnaire)
- drank any alcoholic drinks or used recreational drugs 72 hours before the 1st test day and during the study period.
- drank more than 3 cups of coffee before any test sessions
- glasses are prohibited (contact lenses are okay) for safety purpose for the heading intervention
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Chronic cannabis use and subconcussive head impacts
Group: Chronic cannabis users Criteria: self-reported chronic THC use (average use once per week but not dependent). Urine cannabis test must show positive. Device: Soccer Heading Soccer Heading: Subjects stood approximately 40 feet away from a JUGS soccer ball launcher and participated in 20 consecutive soccer headings, separated by one minute intervals. |
A standardized and reliable soccer heading protocol will be used for the experiment.
A triaxial accelerometer embedded in a head-band pocket and positioned directly below the external occipital protuberance (inion) to monitor linear and rotational head accelerations.
A JUGS soccer machine will be used to simulate a soccer throw-in with a standardized ball speed of 25mph.
The ball speed is similar to when soccer players make a long throw-in from the sideline to mid-field.
Soccer players frequently perform this maneuver during practice and games.
Subjects will stand approximately 40ft away from the machine to perform the heading.
Participants perform 20 standing headers with 1 header per 30 seconds.
The subjects will be instructed to direct the ball back toward the JUGS soccer machine in the air.
|
|
Active Comparator: Non-cannabis use and subconcussive head impacts
Group: Non cannabis users Criteria: self-reported none THC use. Urine cannabis test must show negative. Device: Soccer Heading Soccer Heading: Subjects stood approximately 40 feet away from a JUGS soccer ball launcher and participated in 20 consecutive soccer headings, separated by one minute intervals. |
A standardized and reliable soccer heading protocol will be used for the experiment.
A triaxial accelerometer embedded in a head-band pocket and positioned directly below the external occipital protuberance (inion) to monitor linear and rotational head accelerations.
A JUGS soccer machine will be used to simulate a soccer throw-in with a standardized ball speed of 25mph.
The ball speed is similar to when soccer players make a long throw-in from the sideline to mid-field.
Soccer players frequently perform this maneuver during practice and games.
Subjects will stand approximately 40ft away from the machine to perform the heading.
Participants perform 20 standing headers with 1 header per 30 seconds.
The subjects will be instructed to direct the ball back toward the JUGS soccer machine in the air.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Acute change in brain-derived blood and saliva biomarkers from pre to 24 hour post-heading
Time Frame: Blood samples will be collected at pre- and 24 hour post-heading
|
Blood samples will be collected and centrifuged at 1500 x g for ten minutes at 4 degree celsius. Serum and saliva samples will be aliquoted and stored at -80 degree celsius until analysis. Serum and saliva samples will be assayed for S100B, neurofilament-light (NfL), glial fibrillary acidic protein (GFAP), and tau, and UCH-L1. All expression levels in pg/mL. |
Blood samples will be collected at pre- and 24 hour post-heading
|
|
Acute change in brain-derived blood and saliva biomarkers from pre to 2 hour post-heading
Time Frame: Blood and saliva samples will be collected at pre- and 2 hour post-heading
|
Blood samples will be collected and centrifuged at 1500 x g for ten minutes at 4 degree celsius. Serum and saliva samples will be aliquoted and stored at -80 degree celsius until analysis. Serum and saliva samples will be assayed for S100B, neurofilament-light (NfL), glial fibrillary acidic protein (GFAP), and tau, and UCH-L1. All expression levels in pg/mL. |
Blood and saliva samples will be collected at pre- and 2 hour post-heading
|
|
Acute change in neurocognitive function from pre to 2 hour post-heading
Time Frame: Neurocognitive function will be assessed at pre- and 2 hour post-heading
|
Participants will complete a computerized neurocognitive assessment (Immediate Post-Concussion Assessment and Cognitive Testing).
|
Neurocognitive function will be assessed at pre- and 2 hour post-heading
|
|
Acute change in neurocognitive function from pre to 24 hour post-heading
Time Frame: Neurocognitive function will be assessed at pre- and 24 hour post-heading
|
Participants will complete a computerized neurocognitive assessment (Immediate Post-Concussion Assessment and Cognitive Testing).
|
Neurocognitive function will be assessed at pre- and 24 hour post-heading
|
|
Acute change in ocular-motor function from pre to 2 hour post-heading
Time Frame: Ocular-motor function will be assessed at pre- and 2 hour post-heading
|
Participants will undergo 2 ocular-motor assessments: 1) near-point of convergence and 2) King-Devick Test--a brief assessment of saccadic eye movements, attention, and visual and language processing.
|
Ocular-motor function will be assessed at pre- and 2 hour post-heading
|
|
Acute change in ocular-motor function from pre to 24 hour post-heading
Time Frame: Ocular-motor function will be assessed at pre- and 24 hour post-heading
|
Participants will undergo 2 ocular-motor assessments: 1) near-point of convergence and 2) King-Devick Test--a brief assessment of saccadic eye movements, attention, and visual and language processing.
|
Ocular-motor function will be assessed at pre- and 24 hour post-heading
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Acute change in brain-derived blood and saliva biomarkers from pre to 72 hour post-heading
Time Frame: Blood and saliva samples will be collected at pre- and 72 hour post-heading
|
Blood samples will be collected and centrifuged at 1500 x g for ten minutes at 4 degree celsius. Serum and saliva samples will be aliquoted and stored at -80 degree celsius until analysis. Serum and saliva samples will be assayed for S100B, neurofilament-light (NfL), glial fibrillary acidic protein (GFAP), and tau, and UCH-L1. All expression levels in pg/mL. |
Blood and saliva samples will be collected at pre- and 72 hour post-heading
|
|
Acute change in neurocognitive function from pre to 72 hour post-heading
Time Frame: Neurocognitive function will be assessed at pre- and 72 hour post-heading
|
Participants will complete a computerized neurocognitive assessment (Immediate Post-Concussion Assessment and Cognitive Testing).
|
Neurocognitive function will be assessed at pre- and 72 hour post-heading
|
|
Acute change in ocular-motor function from pre to 72 hour post-heading
Time Frame: Ocular-motor function will be assessed at pre- and 72 hour post-heading
|
Participants will undergo 2 ocular-motor assessments: 1) near-point of convergence and 2) King-Devick Test--a brief assessment of saccadic eye movements, attention, and visual and language processing.
|
Ocular-motor function will be assessed at pre- and 72 hour post-heading
|
|
Acute change in autonomic nerve function from pre to 2 hour post-heading
Time Frame: Autonomic response will be assessed at pre- and 2 hour post-heading
|
Participants will undergo cold-pressor testing (CPT). CPT is a general assessment of the ability of the sympathetic nervous system to become activated. This test will be performed by submerging a participant's hand into cold water for 2 minutes while autonomic and hemodynamic variables are recorded. At each data collection, participants will be instrumented for the measurement of heart rate (electrocardiogram) and continuous blood pressure. Participants will rest quietly for ~10mins before the CPT begins. The test takes 2 minutes. Mean arterial pressure (in mm/Hg) is the outcome measure. |
Autonomic response will be assessed at pre- and 2 hour post-heading
|
|
Acute change in autonomic nerve function from pre to 24 hour post-heading
Time Frame: Autonomic response will be assessed at pre- and 24 hour post-heading
|
Participants will undergo cold-pressor testing (CPT). CPT is a general assessment of the ability of the sympathetic nervous system to become activated. This test will be performed by submerging a participant's hand into cold water for 2 minutes while autonomic and hemodynamic variables are recorded. At each data collection, participants will be instrumented for the measurement of heart rate (electrocardiogram) and continuous blood pressure. Participants will rest quietly for ~10mins before the CPT begins. The test takes 2 minutes. Mean arterial pressure (in mm/Hg) is the outcome measure. |
Autonomic response will be assessed at pre- and 24 hour post-heading
|
|
Acute change in autonomic nerve function from pre to 72 hour post-heading
Time Frame: Autonomic response will be assessed at pre- and 72 hour post-heading
|
Participants will undergo cold-pressor testing (CPT). CPT is a general assessment of the ability of the sympathetic nervous system to become activated. This test will be performed by submerging a participant's hand into cold water for 2 minutes while autonomic and hemodynamic variables are recorded. At each data collection, participants will be instrumented for the measurement of heart rate (electrocardiogram) and continuous blood pressure. Participants will rest quietly for ~10mins before the CPT begins. The test takes 2 minutes. Mean arterial pressure (in mm/Hg) is the outcome measure. |
Autonomic response will be assessed at pre- and 72 hour post-heading
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Mental Disorders
- Chemically-Induced Disorders
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Substance-Related Disorders
- Wounds and Injuries
- Craniocerebral Trauma
- Trauma, Nervous System
- Head Injuries, Closed
- Wounds, Nonpenetrating
- Brain Injuries
- Brain Injuries, Traumatic
- Marijuana Abuse
- Brain Concussion
Other Study ID Numbers
- 2006187939
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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