Exercise Facilitation of Adolescent Fear Extinction, Frontolimbic Circuitry, and Endocannabinoids

Purpose

Anxiety disorders commonly begin during adolescence, and are characterized by deficits in the ability to inhibit or extinguish pathological fear. Recent research has provided new understanding of how fear is learned and can be regulated in the adolescent brain, and how the endocannabinoid system shapes these processes; however, these advances have not yet translated into improved therapeutic outcomes for adolescents with anxiety. This study will test whether a behavioral intervention, acute exercise, can help to improve fear regulation by enhancing brain activity and endocannabinoid signaling. This line of research may ultimately lead to more effect treatments for adolescent anxiety, and to new preventive strategies for at-risk youth.

Condition

  • Adolescence

Eligibility

Eligible Ages
Between 14 Years and 17 Years
Eligible Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  1. Provision of signed and dated informed consent form 2. Stated willingness to comply with all study procedures and available for the duration of the study 3. 14-17 years of age upon enrollment 4. Right-handed 5. In good general health as evidenced by medical history 6. Adolescent and parent/guardian are English-speaking, as study assessments are in English 7. Availability of a parent or legal guardian who is willing to provide consent and attend all study visits

Exclusion Criteria

  1. Traumatic brain injury with ongoing symptoms 2. Sensory (e.g., hearing) or physical (e.g., motor, balance) impairment or significant developmental delay 3. MRI participants: MRI contraindication (e.g., braces, implants, claustrophobia) 4. Any condition that would contraindicate blood draws (e.g., hemophilia, sickle cell) 5. Past or current diagnosis or presence of likely neurological disorder (e.g., epilepsy), psychotic disorder (e.g., schizophrenia, schizoaffective disorder), or bipolar disorder 6. Severe/unstable medical condition (e.g., diabetes, rheumatoid arthritis) 7. Current (past 1-month) use of cannabis or cannabinoid products including CBD unless willing to stop for at least 4 weeks prior to entering the study 8. Currently pregnant, lactating, or positive pregnancy test at screening visit 9. Current homicidal thoughts or suicide attempt in the past year 10. Current suicidal thoughts requiring immediate intervention 11. Concurrent use (past 6 weeks) of oral contraceptives 12. Diagnosed or probable substance use disorder (past 1-month) 13. Positive drug test at baseline visit (e.g., THC, cocaine) 14. Moderate/severe drug or alcohol use in the past 8 weeks 15. Current or recent (past 1-month) COVID-19 diagnosis or febrile illness 16. Treatment with investigational drug or intervention (past 1-month) 17. Current smoker, vaper, or tobacco or nicotine use (past 1-month) 18. Ongoing exposure to abuse

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Basic Science
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Moderate Intensity Exercise
  • Behavioral: Moderate Intensity Exercise
    Participants randomized to the active (moderate intensity) exercise condition will complete a 3-minute warm-up at low speed on a treadmill. Speed and incline will be increased in 3-minute increments until moderate-intensity exercise, defined as participants staying within a zone of 60-80% AAMHR with the target being to attain and maintain 70-75% AAMHR while briskly walking and/or jogging depending on current fitness status, is reached for a total of 30 min.
No Intervention
Control (Coloring)

Recruiting Locations

Tolan Park Medical Building
Detroit, Michigan 48201
Contact:
MacKenna Shampine
313-242-7464‬
mackenna.shampine@wayne.edu

More Details

NCT ID
NCT06297278
Status
Recruiting
Sponsor
Wayne State University