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Not yet recruiting Not applicable NCT07496489

Perceptions of Proposed Warnings for Cannabis Edibles Packaging

No applicable phase (e.g. observational)
Conditions: Cannabis Use

Sponsor: Wake Forest University Health Sciences

trial.available_in: БГ
Overview
The purpose of this study is to compare a delayed-effects warning to an expanded warning developed in previous experiments on knowledge, harm perceptions, and willingness to try cannabis edibles. Additionally, this study will examine the effects of a corresponding icon on attention to and recall of the warning.
Description
Cannabis edibles are rapidly leading the legal recreational cannabis market. The Cannabis edibles present health harms that are not typical of smoked marijuana, including accidental overconsumption of high levels of THC. One effective way to communicate proper dosing and risks of overconsumptions is through package warnings. This experiment will assign participants to view real cannabis edibles packaging with one of four variations of warnings and a series of questions to assess knowledge, harm perceptions, and willingness to try the product shown. One group of participants will serve as the control and will see the same cannabis edibles packaging without a warning.
Who can participate
Inclusion Criteria: * English-speaking by self-selection * United States resident Exclusion Criteria: * Already participated in a precursor project (IRB00104038, IRB000111438) * Eligible but demographic and user group strata have already been met
Interventions
No Warning Control
BEHAVIORAL
Delayed Effects Text Only
BEHAVIORAL
Delayed Effects Plus Icon
BEHAVIORAL
Delayed Effects Plus Dose
BEHAVIORAL
Delayed Effects Plus Dose Plus Adverse Effects
BEHAVIORAL
Locations 1
United States (1)
Wake Forest University Health Sciences
Winston-Salem , North Carolina
Technical details
Status
Not yet recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
65 Years
Healthy volunteers
No
Start date
01.06.2026
Completion date
01.08.2026
Registry ID
NCT07496489
Source
clinicaltrials.gov
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