Effects of Different Cannabis Strains on Perception, Feelings, and Performance
Official title: Effects of Various Cannabis Strains on Perceptual, Subjective and Objective Use Outcomes
Run by Johns Hopkins University · NCT07214155 · Data updated 2026-11-12
This study tests how indica, sativa, or generic cannabis affects thinking, mood, and driving-related performance in adults who already use cannabis.
Quick facts
| Phase | Phase 1 |
|---|---|
| Study type | Interventional |
| Ages | 21 Years to 55 Years |
| Sex | All |
| Enrollment | 70 (estimated) |
| Sponsor | Johns Hopkins University Academic / other |
| Locations | 1 site (Baltimore, Maryland) |
| Status | Recruiting |
| Started | September 15, 2026 |
| Main results expected | June 2029 |
| Study ends | September 2029 |
| Registry record updated | September 18, 2026 |
| Trial ID | NCT07214155 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 21–55 who have prior cannabis experience and meet health criteria, including negative drug and pregnancy tests and controlled blood pressure.
✕Probably not a fit
Individuals without prior cannabis use or with health issues outside inclusion criteria may not experience benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a Phase 1, double-blind, placebo-controlled laboratory study where participants will complete six outpatient sessions. In each session, they will self-administer smoked cannabis labeled as indica, sativa, or generic, at 0 mg or 25 mg THC, in a within-subjects design. Primary outcomes include cognitive and psychomotor performance, subjective effects, and simulated driving performance, along with smoking topography. The trial aims to characterize how different labelings and THC levels influence use outcomes in healthy, adult cannabis users.
Why it matters
Potential benefit: Findings could improve understanding of how cannabis labeling and THC content relate to user experience and safety, informing harm reduction and labeling practices.
How similar studies have gone: Similar randomized, placebo-controlled cannabis studies have shown measurable effects on cognition and driving-related tasks, supporting the feasibility of this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Have provided written informed consent. * Be between the ages of 21 and 55 * Be in good general health based on a physical examination, medical history, vital signs, and screening urine and blood tests * Test negative for drugs of abuse including breath alcohol at the screening visit and at clinic admission * Not be pregnant or nursing (if female). All females must have a negative serum pregnancy test at the screening visit and a negative urine pregnancy test at clinic admission. Participants must confirm use of appropriate birth control methods (e.g., condoms, birth control pills) throughout the entirety of the study. * Blood pressure at Screening Visit does not exceed a systolic blood pressure (SBP) of 150 mmHg or a diastolic blood pressure (DBP) of 90 mmHg * Have prior experience smoking cannabis but not currently using more than 3 times per week on average; participants must be active cannabis users (i.e., report past 3-month use) to participate. Exclusion Criteria: * Self-reported use of illicit drugs (e.g., amphetamine, cocaine, methamphetamine, 3,4-Methylenedioxymethamphetamine (MDMA), lysergic acid diethylamide (LSD), ketamine, heroin, psilocybin, prescription medications not prescribed to the person) in the past 30 days. * History of or current evidence of significant medical (e.g., seizure disorder) or psychiatric illness (e.g. psychosis) judged by the investigator to put the participant at greater risk of experiencing an adverse event due to exposure or completion of other study procedures. * History of clinically significant cardiac arrhythmias or vasospastic disease (e.g., Prinzmetal's angina). * Enrolled in another clinical trial or having received any drug as part of a research study within 30 days prior to dosing. * Having previously sought medical attention to manage adverse effects following acute cannabis use * Individuals with anemia or who have donated blood in the prior 30 days
Where it's running
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Johns Hopkins University
Baltimore, Maryland, United States Recruiting
Study contacts
- Principal investigator: Carlos A Zamarripa, PhD — Johns Hopkins University
- Study coordinator: Carlos A Zamarripa, PhD
- Email: czamarr2@jhmi.edu
- Phone: 410-550-6969
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.