Status:
RECRUITING
Behavioral Pharmacology of Cannabis in Older Adults
Lead Sponsor:
University of Arkansas
Conditions:
Health Services for the Aged
Eligibility:
All Genders
55-70 years
Phase:
PHASE1
Brief Summary
This study examines the effects of cannabis on mood, cognitive and psychomotor performance, balance and vital signs in older adults.
Detailed Description
The overarching aims of this pilot study are to determine the dose-related effects of cannabis and explore feasibility and acceptability of conducting a rigorous behavioral pharmacology study in this ...
Eligibility Criteria
Inclusion
- Self-reported history of marijuana use with no serious adverse effects
- Negative urine toxicology screen for psychoactive drugs (cocaine, fentanyl, methadone, opiates, buprenorphine, methamphetamine, amphetamines, barbiturates, oxycodone, benzodiazepines, phencyclidine, and THC) and CBD
- Negative breath alcohol concentration
- Report ≥1 year abstinence from nicotine and tobacco
- Report ≥1 month of abstinence from THC- and CBD- containing products and be willing to abstain from these products for the study duration
- Blood pressure (BP) reading ≤140/90 and ≥110/70 at the time of screening
- Read and understand English (because assessments are validated in English)
- Menopause as defined as no reported menstruation for ≥12 months (females only)
- Negative urine pregnancy test (females only)
- Stable medical conditions controlled by non-psychoactive medications that do not alter THC/CBD metabolism (e.g., hypertension under control with certain antihypertensives; type II diabetes controlled by metformin)
Exclusion
- A history of moderate to severe substance use disorders (SUDs) (except tobacco), according to the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5), and no recent history (≥1 year) of SUD
- Current tobacco/nicotine use
- ECG abnormalities at screening including but not limited to: bradycardia (\<55 beats per minute); prolonged QTc interval (\>450 msec); Wolff-Parkinson White syndrome; wide complex tachycardia; 2nd degree, Mobitz type II heart block; 3rd degree heart block; left or right bundle branch block; pre-existing severe gastrointestinal narrowing (pathologic or iatrogenic)
- Have a serious and uncontrolled medical condition (major cardiovascular, renal, endocrine, or hepatic disorder) including a history of serious head trauma or neurological disorder (e.g., seizure disorder)
- Meet Diagnostic and Statistical Manual of Mental Disorders (DSM)-5 criteria for lifetime psychosis, schizophrenia, or bipolar disorder or current major depressive disorder, suicidality (e.g., last month suicidal ideation or suicide attempt in past year, as measured by Columbia Suicide Severity Rating Scale) or have significant psychiatric symptoms of another disorder
- Diagnosis of a cognitive disorder (Alzheimer's Disease, dementia) or a score of \<25 on the Montreal Cognitive Assessment (MoCA) for Dementia during screening
- Currently taking any prescribed medication for a psychiatric disorder
- Current use of over-the-counter medication or prescription psychoactive drugs that would be expected to have major interaction with THC (e.g., warfarin, serotonin reuptake inhibitors, tricyclic antidepressants, sildenafil).
- Reported cancer-related fibromyalgia or neuropathic pain conditions
- Have a medical contraindication to, or prior serious adverse events from, cannabis or brownie ingredients (e.g., food sensitivities to gluten/wheat, chocolate, eggs)
- Consume the equivalent of \>2 cups of coffee/day (to reduce variability related to metabolic interactions with caffeine)
- Have any of the following: uncontrolled hypertension (i.e., systolic \>140 mm Hg and/or diastolic \>90 mm Hg on three separate occasions; systolic \>170 or diastolic \>110 on any occasion), liver function tests \>3 times normal, blood urea Nitrogen and Creatinine outside normal range
- Have a physical limitation that will interfere with completing study tasks
- Have child-bearing potential (women)
Key Trial Info
Start Date :
May 1 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 31 2025
Estimated Enrollment :
5 Patients enrolled
Trial Details
Trial ID
NCT06055309
Start Date
May 1 2025
End Date
December 31 2025
Last Update
November 3 2025
Active Locations (1)
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1
University of Arkansas for Medical Science
Little Rock, Arkansas, United States, 72205