Clinical trial Recruiting at 1 site Phase 1 Interventional Ages 21 to 55

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

PhasePhase 1
Study typeInterventional
Ages21 Years to 55 Years
SexAll
Enrollment70 (estimated)
SponsorJohns Hopkins University
Academic / other
Locations1 site (Baltimore, Maryland)
StatusRecruiting
StartedSeptember 15, 2026
Main results expectedJune 2029
Study endsSeptember 2029
Registry record updatedSeptember 18, 2026
Trial IDNCT07214155 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

  • 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • Brain imaging to predict teens' response to cannabis treatment

    This project will test whether teens' brain activity during a learning task can predict how well 14–17-year-olds do in a 10-week virtual reward program to reduce cannabis use.

    Recruiting Indiana University · Indianapolis, Indiana · NCT07340554

  • Pregnenolone to treat cannabis intoxication

    This trial tests whether oral pregnenolone can quickly reverse cannabis intoxication symptoms in healthy adults with prior cannabis use.

    Recruiting Phase 2 Johns Hopkins University · Baltimore, Maryland · NCT07216690

  • Oral saliva testing to detect recent cannabis use in young adults.

    This project will test whether at-home saliva tests can detect recent cannabis use in 18-to-30-year-olds who use cannabis at least once a week.

    Recruiting Boston Children's Hospital · Boston, Massachusetts · NCT06891235

  • Effects of vaporized cannabis and alcohol on impairment

    This study is testing how using alcohol and vaporized cannabis together affects people's ability to think and act, to help understand the risks of mixing these substances.

    Recruiting Phase 1 Johns Hopkins University · Baltimore, Maryland · NCT06293040

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.